US20160151405A1 - Pappalysin Regulator - Google Patents

Pappalysin Regulator Download PDF

Info

Publication number
US20160151405A1
US20160151405A1 US14/889,997 US201414889997A US2016151405A1 US 20160151405 A1 US20160151405 A1 US 20160151405A1 US 201414889997 A US201414889997 A US 201414889997A US 2016151405 A1 US2016151405 A1 US 2016151405A1
Authority
US
United States
Prior art keywords
pappalysin
stanniocalcin
polypeptide
papp
stc2
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US14/889,997
Other languages
English (en)
Inventor
Claus Oxvig
Jakob Hauge Mikkelsen
Malene Runge JEPSEN
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aarhus Universitet
Original Assignee
Aarhus Universitet
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aarhus Universitet filed Critical Aarhus Universitet
Assigned to AARHUS UNIVERSITET reassignment AARHUS UNIVERSITET ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: MIKKELSEN, JAKOB HAUGE, JEPSEN, Malene Runge, OXVIG, CLAUS
Publication of US20160151405A1 publication Critical patent/US20160151405A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • A61K31/713—Double-stranded nucleic acids or oligonucleotides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/22—Hormones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/575—Hormones
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
    • C07K16/38—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against protease inhibitors of peptide structure
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
    • C07K16/40—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against enzymes
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
    • C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
    • C12N9/6489—Metalloendopeptidases (3.4.24)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y304/00—Hydrolases acting on peptide bonds, i.e. peptidases (3.4)
    • C12Y304/24—Metalloendopeptidases (3.4.24)
    • C12Y304/24079—Pappalysin-1 (3.4.24.79)
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor

Definitions

  • the present invention relates to interaction and complex formation between Pappalysin and stanniocalcin, and the use of stanniocalcin as regulator of Pappalysins.
  • PAPP-A pregnancy associated plasma protein-A
  • IGF insulin-like growth factor
  • PAPP-A is, based on its primary structure, characterized as a metalloproteinase belonging to the metzincin superfamily. However, PAPP-A also has features differing from other metzincins, and therefore it is categorized into a subgroup of metzincins called the pappalysins, which also includes the PAPP-A homologue PAPP-A2.
  • PAPP-A Pregnancy-associated plasma protein-A
  • the protein was of placental origin and was found in serum of pregnant women.
  • the concentration of PAPP-A increases during pregnancy, and reduced levels of PAPP-A in the maternal circulation in the first trimester of pregnancy correlates with high risks of fetal Down's syndrome making PAPP-A a clinical marker for trisomy 21.
  • low PAPP-A concentrations in maternal pregnancy serum have been associated with high risks of trisomy 18, pre-eclampsia and low birth weight of full-term babies.
  • PAPP-A is the protease responsible for IGF dependent proteolytic activity against IGFBP-4. PAPP-A also specifically cleaves IGFBP-5, and to some extent IGFBP-2. In particular, no other proteinases have been shown to physiologically process IGFBP-4. PAPP-A mediated cleavage of IGFBP-4 is significantly accelerated by the presence of IGF. Cleaved IGFBP fragments have decreased affinity towards IGF and PAPP-A proteolytic activity consequently results in release of bioactive IGF capable of binding and activating the IGF-I receptor. Thus, PAPP-A functions as an IGFBP antagonist.
  • PAPP-A is secreted from the placenta as a dimer of 400 kDa, but circulates primarily as a disulfide bound 2:2 complex with the proform of eosinophil major basic protein (proMBP) of 500 kDa.
  • proMBP eosinophil major basic protein
  • PAPP-A activity against IGFBP-4 is inhibited by polyclonal antibodies raised against PAPP-A/proMBP.
  • agents capable of chelating divalent cations such as EDTA and 1,10-phenantroline, are general unspecific inhibitors of metalloproteinases and thus abolish PAPP-A proteolytic activity as well (Overgaard 2000).
  • phage derived single chain fragment variable (scFv) antibodies have been shown to inhibit PAPP-A proteolysis of IGFBP-4 through targeting of LNR3, which consequently is considered to be an exosite of PAPP-A.
  • the LNR3 module is located in the C-terminal end of PAPP-A.
  • PAPP-A is a potential target in therapeutical control of IGF signaling
  • LNR3 targeting by antibodies demonstrates a way of selectively inhibiting IGFBP-4 proteolysis.
  • proMBP is the only known physiological inhibitor of PAPP-A.
  • the present invention relates to aspects of using stanniocalcin as inhibitor of the proteolytic activity of Pappalysin, as well as other aspects of using the interaction between stanniocalcin and Pappalysins.
  • Pappalysins comprise PAPP-A and PAPP-A2 polypeptides, as well as fragments and variants thereof. Specifically, Pappalysins may form dimers of PAPP-A subunits, PAPP-A2 subunits or fragments or variants thereof, or Pappalysin heterodimers of PAPP-A and PAPP-A2 or fragments or variants thereof.
  • the present invention relates to a method of decreasing or increasing the activity of a Pappalysin polypeptide by decreasing or increasing the level of interacting Pappalysin and stanniocalcin polypeptides.
  • the activity of a Pappalysin polypeptide is increased by administering an agent, which antagonizes the interaction of stanniocalcin with Pappalysin, for example a stanniocalcin directed siRNA or an antibody, such as an antibody capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • an agent which antagonizes the interaction of stanniocalcin with Pappalysin
  • the activity of Pappalysin polypeptide is inhibited by providing a stanniocalcin polypeptide, for example using a nucleic acid vector expressing said stanniocalcin polypeptide or part thereof, for example using a retroviral vector, or by providing a stanniocalcin polypeptide in the form of purified or partly purified stanniocalcin.
  • the activity of Pappalysin polypeptide correlates negatively with the level of stanniocalcin and thus, the activity of Pappalysin polypeptide may be decreased by increasing the level of a stanniocalcin polypeptide, and increased by decreasing the level of a stanniocalcin polypeptide.
  • the method is performed by increasing or decreasing the level of stanniocalcin polypeptide in a human cell, such as in a human stem cell.
  • the method can be applied to increase or decrease the level of a stanniocalcin polypeptide in a mammalian subject, such as in a human being, such as in a specific tissue of a mammalian subject, such as human being, for example a cancer tissue.
  • a method is provided of preventing, treating or ameliorating a clinical condition in a mammalian subject, such as a human being, said method comprising administering to said mammalian subject, such as human being an effective amount of a stanniocalcin polypeptide.
  • a mammalian subject such as a human being
  • administering to said mammalian subject, such as human being an effective amount of a stanniocalcin polypeptide.
  • This method serves to inhibit a proliferative process, and thus, the method is preferably applied for prevention, treatment or amelioration of a proliferative disorder, such as cancer, for example ovarian cancer, testicular cancer, lung cancer, or any cancer of the digestive system, including ventricular cancer, colon cancer, small bowel cancer and rectal cancer, in particular, the cancer is selected from the group consisting of ovarian cancer, lung cancer and colon cancer.
  • a proliferative disorder such as cancer, for example ovarian cancer, testicular cancer, lung cancer, or any cancer of the digestive system, including ventricular cancer, colon cancer, small bowel cancer and rectal cancer, in particular, the cancer is selected from the group consisting of ovarian cancer, lung cancer and colon cancer.
  • Other preferred clinical conditions include restenosis, atherosclerosis, ovulation, fibrosis, as well as clinical conditions related to human reproduction.
  • Other preferred clinical conditions include fluid accumulation, such as ascites production in ovarian cancer patients.
  • the present invention pertains to a method of preventing, treating or ameliorating a clinical condition in a mammalian subject, such as in a human being, said method comprising administering to said mammalian subject, such as human being an effective amount of an agent capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • an agent capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • Interactions between stanniocalcin and Pappalysin polypeptides are preferably antagonized by providing an antibody, such as a blocking antibody, which inhibits the interaction of stanniocalcin with Pappalysin.
  • an antibody which is capable of specifically binding interacting stanniocalcin and Pappalysin polypeptides, such as a non-covalent interaction between PAPP-A and stanniocalcin 1 and/or a covalent complex between PAPP-A and stanniocalcin 2.
  • the antibody preferably has a higher affinity for said complex consisting of or comprising a Pappalysin polypeptide and a stanniocalcin polypeptide than Pappalysin or stanniocalcin individually. This antibody can be used for detection of interacting stanniocalcin and Pappalysin polypeptides.
  • the antibody can also be used for stabilizing or promoting the formation of a covalent or non-covalent complex between Pappalysin and stanniocalcin, and thereby serve to inhibit Pappalysin.
  • an antibody which is capable of antagonizing the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide, for example by binding the Pappalysin polypeptide and/or a stanniocalcin polypeptide.
  • the invention also in one aspect provides an agent or a pharmaceutical composition
  • an agent which agent is capable of increasing or decreasing the level of a stanniocalcin polypeptide, and/or capable of antagonizing or promoting the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide for use in medicine.
  • agent is for example a stanniocalcin polypeptide or part thereof, an siRNA targeting stanniocalcin or an antibody of the invention.
  • the agent is used in wound healing and/or bone remodeling or bone growth (e.g.
  • the agent in the treatment of bone fractures), and/or the agent is used in the treatment of a restenosis, atherosclerosis, ovulation, fibrosis, or cancer, such as ovarian cancer, testicular cancer, lung cancer, or any cancer of the digestive system, including ventricular cancer, colon cancer, small bowel cancer and rectal cancer.
  • the invention in another aspect relates to a method of producing a composition comprising Pappalysin polypeptide, wherein said composition is essentially devoid of stanniocalcin polypeptide, said method comprising removing stanniocalcin and/or covalent and non-covalent complexes of Pappalysin and stanniocalcin from a composition comprising Pappalysin and said complexes of Pappalysin and stanniocalcin.
  • This aspect relates to a method of producing a composition comprising Pappalysin polypeptide, wherein said composition is essentially devoid of stanniocalcin polypeptide and complexes comprising stanniocalcin polypeptide, said method comprising the steps of
  • the invention also relates in a separate aspect to a composition obtainable by the method above.
  • the present invention relates to a composition comprising Pappalysin, wherein said composition is essentially free of stanniocalcin.
  • the invention provides a method for quantifying the level of Pappalysin in a sample, said method comprising using a homogenous composition essentially free of stanniocalcin as a standard.
  • a method is provided comprising the steps of
  • the invention provides a Pappalysin polypeptide interacting with at least one stanniocalcin polypeptide.
  • the interaction is in one embodiment a non-covalent interaction between PAPP-A and stanniocalcin 1 and/or a covalent interaction between PAPP-A and stanniocalcin 2; and/or a non-covalent interaction between PAPP-A2 and stanniocalcin 1 and/or a covalent interaction between PAPP-A2 and stanniocalcin 2.
  • the present invention relates to a method of producing an antibody specific for interacting Pappalysin and stanniocalcin polypeptides, said method comprising
  • the invention provides in one aspect a method of identifying an agent capable of promoting or antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide, said method comprising
  • an agent is identified, which is capable of binding interacting Pappalysin and stanniocalcin polypeptides with higher affinity than Pappalysin or stanniocalcin alone, by a method comprising
  • an agent is identified, which is capable of binding a polypeptide region of a Pappalysin or stanniocalcin polypeptide, which region is not surface exposed in interacting Pappalysin and stanniocalcin polypeptides, by a method comprising
  • an agent is identified, which is capable of binding an unbound Pappalysin polypeptide, wherein said agent binds Pappalysin in a region comprising the binding site for stanniocalcin, by a method comprising
  • an agent is identified, which is capable of binding unbound stanniocalcin polypeptide, wherein said agent binds stanniocalcin in a region comprising the binding site for Pappalysin, by a method comprising
  • the invention also in one aspect provides a method of detecting an interaction between a Pappalysin polypeptide and a stanniocalcin polypeptide in a sample, said method comprising
  • the invention in one aspect pertains to a method of determining a clinical condition, said method comprising detecting interacting Pappalysin and stanniocalcin polypeptides, such as PAPP-A and stanniocalcin 1 interacting non-covalently and/or a covalent complex between PAPP-A and stanniocalcin 2.
  • the clinical condition is for example a cancer, such as ovarian cancer, testicular cancer, lung cancer, or any cancer of the digestive system, including ventricular cancer, colon cancer, small bowel cancer and rectal cancer.
  • a cancer such as ovarian cancer, testicular cancer, lung cancer, or any cancer of the digestive system, including ventricular cancer, colon cancer, small bowel cancer and rectal cancer.
  • a stanniocalcin polypeptide preferably is selected from the group consisting of
  • a Pappalysin polypeptide is preferably selected from the group consisting of
  • FIG. 1 Western blots detecting STC1 and STC2—Visualization of the covalent PAPP-A/STC2 complex.
  • FIG. 2 Western blots detecting PAPP-A during co-expression with STC1 or STC2.
  • Samples were culture supernatant from transfected cells.
  • Cells were transfected with empty plasmid DNA (mock) or co-transfected with PAPP-A and empty plasmid DNA, STC1 (A), or STC2 (B) cDNA.
  • PAPP-A Antibodies (Ab) were used for PAPP-A detection.
  • White arrows in A) and B) point out the disappearance of high molecular weight (HMW) and low molecular weight (LMW) PAPP-A bands, respectively.
  • HMW high molecular weight
  • LMW low molecular weight
  • FIG. 3 Detection of PAPP-A/STC2 complex formation.
  • Mixtures of PAPP-A and STC2 (A) or PAPP-A and mock (B) medium taken out at the indicated time points were analyzed by Western blotting.
  • Conditioned medium from mock transfected cells or cells co-transfected with PAPP-A and STC2 cDNA (PA+STC2 co-tf) were loaded as controls.
  • PAPP-A antibodies were used for PAPP-A detection.
  • the localization of PAPP-A and PAPP-A in complex with STC2 is depicted. ON indicates overnight incubation. It is evident from B that a non-saturating level of endogenous stanniocalcin 2 is present in the medium.
  • FIG. 4 Detection of STC2 protein in PAPP-A samples.
  • FIG. 5 SDS-PAGE of eluted fractions of purified STC1 and STC2.
  • Purified STC1 A) and STC2 B) protein was eluted in 10 fractions.
  • Fractions #1-6 were separated by SDS-PAGE.
  • a sample of the wash eluate before protein elution and an EDTA sample from the final column stripping were loaded. After electrophoresis gels were stained with coomassie brilliant blue.
  • FIG. 6 Inhibition of PAPP-A proteolytic activity against IGFBP-4 by STC1 and STC2. PAPP-A in culture supernatant was pre-incubated with mock-, STC1- or STC2-medium
  • FIG. 7 Identification of PAPP-A interaction partner by MALDI-TOF mass spectrometry.
  • Total PAPP-A was immunoprecipitated from the medium of a human cancer cell line using a monoclonal PAPP-A antibody. The precipitated material appeared as two bands in non-reducing SDS-PAGE. In the lower band of 400 kDa, only peptides derived from PAPP-A were identified. Apart from PAPP-A, the upper band also contained Stanniocalcin peptides.
  • FIG. 8 PAPP-A western blot.
  • PAPP-A was incubated ON at 37 C with conditioned medium from either mock, STC2, or mutated STC2, in which cysteine 120 is replaced with an alanine residue (C120A).
  • Samples were separated by SDS-PAGE, blotted onto a PVDF membrane and bands visualized with polyclonal anti-PAPP-A antibodies. No band-shift is observed with the C120A mutant, demonstrating that cysteine 120 of STC2 is responsible for the formation of a covalent disulphide complex with PAPP-A.
  • FIG. 11 STC1 and STC2 inhibit the proteolytic activity of PAPP-A.
  • a PAPP-A proteolytic activity towards radiolabeled IGFBP-4 in media from HEK293T cells transfected with combinations of cDNAs as indicated.
  • b PAPP-A Western blot of samples from a.
  • c PAPP-A proteolytic activity towards radiolabeled IGFBP-4 in the presence or absence of purified STC1 or STC2 added at the beginning of the cleavage reaction.
  • Right panel Coomassie-stained SDS-PAGE gels of purified proteins.
  • d Surface plasmon resonance analysis of STC1 binding to PAPP-A.
  • e Kinetic analysis of STC1 inhibition of PAPP-A cleavage of IGFBP-4. All gel images and the immunoblot are representative of at least four independent experiments.
  • FIG. 12 Inhibition of PAPP-A by STC2 requires covalent complex formation.
  • a PAPP-A Western blot of medium from HEK293T cells transfected with combinations of cDNAs as indicated.
  • b STC2 Western blot of samples from a.
  • c PAPP-A Western blot of medium from HEK293T cells transfected with combinations of cDNAs.
  • d PAPP-A Western blot of separately synthesized PAPP-A and STC2 incubated for 0-16 h.
  • e PAPP-A proteolytic activity towards radiolabeled IGFBP-4 in 16 h-samples from d.
  • f PAPP-A Western blot of separately synthesized PAPP-A and STC1 incubated for 0-16 h.
  • the immunoblots and the gel image are representative of at least four independent experiments.
  • FIG. 13 Covalent binding to PAPP-A is mediated by C120 of STC2.
  • a STC2 Western blot of wild-type and mutated variants of STC2 as indicated.
  • b PAPP-A Western blot of media from HEK293T cells transfected with combinations of cDNAs.
  • c Kinetic analysis of STC2(C120A) inhibition of PAPP-A cleavage of IGFBP-4.
  • d Assessment of IGF-I receptor stimulation in vitro by combinations of IGF-I, IGFBP-4, PAPP-A and STCs. Quantified signals normalized to the signal with IGF-I alone are shown to the right. Results are means ⁇ s.d. from four independent experiments. ns, not statistically significant.
  • FIG. 14 Overexpression of STC2, but not STC2(C120A), causes growth retardation in mice.
  • a Growth curves of nontransgenic and STC2 transgenic female mice divided into groups according to circulating levels of STC2. Results are means with s.d. indicated. Statistical significance is based on comparison of mice older than three weeks.
  • b Body weight of STC2 transgenic female mice at week five as a function of measured levels of circulating transgene-derived STC2.
  • c Growth curves of nontransgenic and STC2(C120A) transgenic female mice. Results are means with s.d.
  • FIG. 15 STC1 and STC2 lack inhibitory activity towards selected proteolytic enzymes outside the pappalysin family, but inhibit PAPP-A2.
  • a Proteolytic cleavage of radiolabeled IGFBP-5 by matrix metalloproteinase-2 (MMP2, a metzincin metalloproteinase) preincubated (8 h) with buffer, STC1, STC2, or EDTA. Contrary to IGFBP-4, IGFBP-5 is promiscuously cleaved by many proteinases.
  • MMP2 matrix metalloproteinase-2
  • EDTA a metzincin metalloproteinase
  • b As a, but using matriptase (a serine proteinase) and trypsin (a serine proteinase) and phenylmethylsulfonyl fluoride (PMSF).
  • PMSF phenylmethylsulfonyl fluoride
  • FIG. 16 Sequence alignment of human STC1 and STC2. Sequence alignment of human STC1 (NM_003155.2) and STC2 (NM_003714.2) using Clustal Omega (http://www.clustal.org/omega/). Disulfide bonds and dimerization disulfide of STC1, indicated by lines, are according to published datal6. Cysteine residues of STC2 (C120, C197, and C205), which have no counterpart in STC1, are indicated with blue color.
  • FIG. 17 Circular dichroism analysis of purified STC2 and STC2(C120A).
  • a Temperature scans showing changes in mean residue ellipticity at 222 nm.
  • b Spectra recorded at 25° C. and 95° C., and at 25° C. following incubation at 95° C. for 2 min.
  • FIG. 18 Assessment of STC2 and STC2(C120A) antibody reactivity. The relative binding of available monoclonal antibodies to STC2 and STC2(C120A) is plotted. A value of 1 indicates equal binding to STC2 and STC2(C120A). Results are means ⁇ s.d. from four independent experiments performed in triplicate. Differences in ratios are not statistically significant.
  • FIG. 19 Murine PAPP-A and PAPP-A2 are inhibited by STC1 and STC2, but not STC2(C120A). a, Proteolytic activity towards radiolabeled IGFBP-4 in medium from
  • HEK293T cells transfected with cDNA encoding murine PAPP-A (mPAPP-A), preincubated with or without STC1, STC2, or STC2(C120A).
  • Right panel Western blot demonstrating covalent complex formation between murine PAPP-A and STC2, but not STC2(C120A).
  • b Kinetic analysis of STC2(C120A) inhibition of murine PAPP-A.
  • c Proteolytic activity towards radiolabeled IGFBP-5 in medium from HEK293T cells transfected with cDNA encoding murine PAPP-A2 (mPAPP-A2), preincubated with or without STC1, STC2, or STC2(C120A). All gel images and the immunoblot are representative of at least four independent experiments.
  • the present inventors have identified stanniocalcin polypeptides as inhibitors of pregnancy-associated plasma protein-A (PAPP-A).
  • the general inventive concept of the present invention relates to a novel complex of Pappalysin and stanniocalcin polypeptides.
  • the present invention relates to the application of this complex in different methods and products, which involves the complex.
  • aspects of the invention relates to the use of the complex between Pappalysins and stanniocalcin polypeptides, as well as methods of producing and screening agents, capable of specifically binding the complex.
  • interacting Pappalysin and stanniocalcin polypeptides refers to at least one Pappalysin polypeptide, which interacts with at least one stanniocalcin polypeptide, or at least one stanniocalcin polypeptide, which interacts with at least one Pappalysin polypeptide.
  • interacting Pappalysin and stanniocalcin polypeptides comprise two Pappalysin polypeptides and two stanniocalcin polypeptides.
  • stanniocalcin may be a recombinantly produced monomer in which one or more cysteine residues are mutated to prevent covalent dimerization.
  • unbound as used herein in relation Pappalysin and stanniocalcin polypeptides refers to any of said respective polypeptides which does not interact with the other.
  • unbound Pappalysin polypeptide refers herein generally to Pappalysin polypeptide, which does not interact with stanniocalcin.
  • unbound stanniocalcin polypeptide refers herein generally to stanniocalcin polypeptide, which does not interact with Pappalysin. In this connection, it is disregarded whether any of Pappalysin and/or stanniocalcin polypeptides may have any other interaction partners.
  • the present inventors have surprisingly found that Pappalysin and stanniocalcin polypeptides interact both covalently and non-covalently.
  • a main aspect of the present invention relates to interacting Pappalysin and stanniocalcin polypeptides.
  • Pappalysins are proteolytic enzymes, and include the metalloproteases PAPP-A and
  • PAPP-A2 specifically cleaves IGF-binding proteins, such as IGFBP-4 and IGFBP-5.
  • IGFBP-4 and IGFBP-5 The cleaved IGFBP fragments have decreased affinity towards IGF and PAPP-A proteolytic activity consequently results in release of bioactive IGF capable of binding and activating the IGF receptor.
  • Activation of the IGF receptor triggers an activation pathway, which leads to e.g. cellular proliferation.
  • the term “Pappalysin” is meant to include both PAPP-A and PAPP-A2 polypeptides.
  • the term includes Pappalysin polypeptides of any species, and therefore encompasses any mammalian Pappalysin protein; i.e. any polypeptide with homology to the human PAPP-A and human PAPP-A2, which particularly also includes mouse PAPP-A and mouse PAPP-A2.
  • the term “Pappalysin” also encompasses variants and fragments of any PAPP-A and PAPP-A2 polypeptides. The term encompasses both monomeric and multimeric forms of the polypeptides, both homomeric and heteromeric multimers.
  • Pappalysins may form homodimers of PAPP-A or PAPP-A2 or fragments or variants thereof, or Pappalysin heterodimers of PAPP-A and PAPP-A2 or fragments or variants thereof.
  • PAPP-A and PAPP-A2 as used herein, is meant to encompass homologous polypeptides of human PAPP-A and PAPP-A2 of any species, respectively, in particular mammalian PAPP-A and PAPP-A2, such as mouse or human PAPP-A and PAPP-A2, with human PAPP-A and PAPP-A2 being most preferred.
  • a Pappalysin polypeptide is a human Pappalysin or a fragment or variant thereof; specifically, the Pappalysin polypeptide is selected from the group consisting of
  • the Pappalysin polypeptide is PAPP-A, such as human PAPP-A, and in another preferred embodiment, the Pappalysin polypeptide is
  • variants of Pappalysin polypeptides include variants having at least 60%, such as at least 65%, such as at least 70%, for example at least 75%, for example at least 80, such as at least 85%, 86%, 76%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, such as at least 96%, 97%, 98%, or 99%, or 99.5% identity to any one of PAPP-A (SEQ ID NO: 3) or PAPP-A2 (SEQ ID NO: 4).
  • a variant has at least 90% identity, such as at least 95% or at least 98% identity to PAPP-A or PAPP-A2, such as human PAPP-A or PAPP-A2.
  • a Pappalysin polypeptide includes the full-length PAPP-A and PAPP-A2 polypeptides and any variants thereof, as well as any fragments of said full-length PAPP-A and PAPP-A2 polypeptides and variants thereof.
  • Fragments of PAPP-A, PAPP-A2 or variants thereof usually comprise or consist of at least 5 consecutive amino acids selected from PAPP-A or PAPP-A2, such as human PAPP-A or PAPP-A2.
  • Fragments may comprise at least 5, such as at least 25, for example at least 50, such as at least 75, for example at least 100, such as at least 200, at least 300, at least 400, at least 500, at least 600, at least 700, at least 800, at least 900, at least 1000, at least 1100, at least 1200, at least 1300, or at least 1400, such as at least 1500 consecutive amino acids selected from PAPP-A, PAPP-A2 or variants thereof.
  • fragments of the invention may comprise less than 1500, such as less than 1400, less than 1300, less than 1200, less than 1100, less than 1000, less than 900, less than 800, less than 700, less than 600, less than 500, less than 400, less than 300, less than 200, less than 100, less than 75 or less than 50, such as less than 25, such as less than 10 consecutive amino acids selected from PAPP-A, PAPP-A2 or variants thereof.
  • Pappalysin fragment of the invention depends on the specific use of the fragment. Pappalysin fragments used for immunization do not necessarily require the full length enzyme. However, methods of detecting a Pappalysin polypeptide in a biological sample, generally aims at detecting biologically native Pappalysins, which are usually full-length.
  • the variants and/or fragments of PAPP-A and PAPP-A2 are functional fragments, in particular metalloproteolytic fragments being able to cleave an IGFBP, such as IGFBP4 and/or IGFBP5.
  • Stanniocalcins are glycoproteins, which include stanniocalcin 1 (STC1) and stanniocalcin 2 (STC2).
  • STC1 and STC2 hSTC1 and hSTC2
  • hSTC1 and hSTC2 are homodimeric glucoproteins, with subunits of approximately 30-35 kDa and 35-40 kDa, respectively.
  • the mature STC1 protein is 247 amino acids long, while the STC2 protein is longer and consists of 302 amino acids.
  • the N-terminal part of newly synthesized STCs is hydrophobic and functions as a signal peptide for protein secretion. The STCs are conserved among a wide range of eukaryotes.
  • STC2 Blast searches of STC reveal, that the proteins have unique amino acid sequences with no recognizable protein motifs, and it is consequently impossible to predict the biochemical functions of the STCs based on their sequences. Furthermore, the amino acid sequence of STC2 is less than 30% identical to STC1 for a given species. There is, however, some degree of sequence homology between STC1 and STC2, including conservation of glycosylation sites. In addition, all 11 cysteine residues found in STC1 appear to be conserved in STC2. Furthermore, the exon-intron boundaries are conserved between the STCs, suggesting derivation from a common ancestral gene.
  • STC2 has a total of 14 cysteine residues, and compared to STC1, human STC2 has an elongated C-terminal containing a histidine cluster (HHxxxxHH), capable of coordinating divalent metal ions.
  • stanniocalcin or “STC” is meant to include both stanniocalcin 1 (STC1) and stanniocalcin 2 (STC2) polypeptides.
  • STC1 stanniocalcin 1
  • STC2 stanniocalcin 2
  • the term includes Stanniocalcin polypeptides of any species, and therefore encompasses any mammalian Stanniocalcin protein; i.e. any stanniocalcin polypeptide with homology to human STC1 and human STC2, which particularly also includes mouse STC1 and mouse STC2.
  • stanniocalcin or “STC” also encompasses variants and fragments of any STC1 and STC2 polypeptides.
  • stanniocalcins may form homodimers of STC1 and/or dimers of STC2 or fragments or variants thereof, or stanniocalcin heterodimers of STC1 and STC2 or fragments or variants thereof.
  • STC1 and STC2 as used herein, is meant to encompass homologous polypeptides of human STC1 and STC2 of any species, respectively, in particular mammalian STC1 and STC2, such as mouse or human STC1 and STC2, with human STC1 and STC2 being most preferred.
  • a stanniocalcin polypeptide is a human stanniocalcin or a fragment or variant thereof; specifically, the stanniocalcin polypeptide of the methods, antibodies, agents, compositions and polypeptides of the present invention is selected from the group consisting of
  • the stanniocalcin polypeptide is STC1
  • the stanniocalcin polypeptide is STC2.
  • Variants of stanniocalcin polypeptides include variants having at least 70%, such as at least 75%, for example at least 80, such as at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, such as at least 96%, 97%, 98%, or 99%, or 99.5% identity to any one of STC1 (SEQ ID NO: 1) or STC2 (SEQ ID NO: 2).
  • a variant has at least 90% identity, such as at least 95% or at least 98% identity to STC1 or STC2, such as human STC1 or STC2.
  • a stanniocalcin polypeptide includes the full-length STC1 and STC2 polypeptides, such as human STC1 or STC2, and any variants thereof, as well as any fragments of said full-length STC1 and STC2 polypeptides and variants thereof. Fragments of STC1, STC2 or variants thereof usually comprise or consist of at least 5 consecutive amino acids selected from STC1 or STC2.
  • Fragments may comprise at least 5, such as at least 15, such as at least 20, such as at least 25, such as at least 30, such as at least 40, such as at least 50, such as at least 60, such as at least 70, such as at least 80, for example at least 90, such as at least 100, such as at least 110, such as at least 120, such as at least 130, such as at least 140, such as at least 150, such as at least 160, such as at least 170, such as at least 180, such as at least 190, such as at least 200 consecutive amino acids selected from STC1, STC2 or variants thereof.
  • fragments of the invention may comprise less than 200, less than 190, less than 180, less than 170, less than 160, less than 150, less than 140, less than 130, less than 120, less than 110, less than 100, less than 90 or less than 80, such as less than 70, such as less than 60, such as less than 50, such as less than 40, such as less than 30, such as less than 25, such as less than 20, such as less than 15, such as less than 10 consecutive amino acids selected from STC1, STC2 or variants thereof, such as human STC1 or STC2 or variants thereof.
  • a stanniocalcin fragment of the invention depends on the specific use of the fragment. Pappalysin fragments used for immunization do not necessarily require the full length enzyme. However, methods of detecting a stanniocalcin polypeptide in a biological sample, generally aims at detecting biologically native stanniocalcin, which are usually full-length.
  • the variants and/or fragments of STC1 and STC2 are functional fragments, in particular such variants or fragments which are capable of interacting with a Pappalysin.
  • STC1 variants and fragments are preferably capable of interacting non-covalently with PAPP-A
  • STC2 variants and fragments are preferably capable of forming covalent complexes with PAPP-A.
  • the STC polypeptide is a polypeptide fragment of STC2, which comprise at least C120, i.e. amino acid residue corresponding to cysteine-120.
  • Pappalysin and stanniocalcin polypeptides interact both non-covalently and covalently.
  • the invention relates to a Pappalysin polypeptide interacting with at least one stanniocalcin polypeptide.
  • the interaction is a non-covalent interaction.
  • the interaction is a covalent complex between a Pappalysin polypeptide and a stanniocalcin polypeptide.
  • a non-covalent interaction is provided between PAPP-A or PAPP-A2 and stanniocalcin 1, i.e.
  • the invention provides a PAPP-A or a PAPP-A2 polypeptide interacting non-covalently with a STC1 polypeptide.
  • a covalent complex between PAPP-A or PAPP-A2 and STC2 is provided.
  • the invention in one aspect provides a method of detecting an interaction between a Pappalysin polypeptide and a stanniocalcin polypeptide in a sample.
  • Such method may use detecting agents with affinity for Pappalysin polypeptide, stanniocalcin polypeptide and/or for interacting Pappalysin and stanniocalcin polypeptides.
  • Antibodies are specifically suitable agents, as antibodies can be raised with specific activity against specific proteins, while also being easily detectable.
  • the method comprises the steps of
  • an antibody which has specific activity for interacting Pappalysin and stanniocalcin polypeptides; i.e. such antibody has no or little affinity for individual Pappalysin and stanniocalcin polypeptides, and has high affinity for interacting Pappalysin and stanniocalcin polypeptides, both non-covalently interacting polypeptides and/or for covalent complexes comprising or consisting of Pappalysin and stanniocalcin polypeptides.
  • Such antibodies are also encompassed by the present invention, as described elsewhere herein, and in a preferred embodiment, such antibodies of the present invention are employed in the detection method of the invention.
  • the method for detecting interacting Pappalysin and stanniocalcin polypeptides employs at least two different antibodies, wherein one antibody has affinity for one of the Pappalysin and stanniocalcin polypeptides and another antibody has affinity for the other of said Pappalysin and stanniocalcin polypeptides; e.g. one antibody has affinity for Pappalysin and another antibody has affinity for stanniocalcin or vice versa.
  • the first antibody could be a catching antibody in an ELISA assay, and the second antibody a detection antibody.
  • a detection method which comprise the steps of
  • interacting Pappalysin and stanniocalcin polypeptides is a non-covalent interaction between PAPP-A and stanniocalcin 1 and/or a covalent complex between PAPP-A and stanniocalcin 2.
  • interacting Pappalysin and stanniocalcin polypeptides is a non-covalent interaction between PAPP-A2 and stanniocalcin 1 and/or a covalent complex between PAPP-A2 and stanniocalcin 2.
  • the sample could be a biological sample obtained from a mammalian subject, such as a human being, for example a blood sample or a tissue sample.
  • the method may also be used for detecting the amount of interacting Pappalysin and stanniocalcin polypeptides secreted from a cell culture.
  • the sample can be culture medium of such a cell culture.
  • the method may also be used for screening for agents capable of modulating (i.e. stimulating or preventing) the formation of covalent and/or non-covalent complex, as described elsewhere herein.
  • compositions of Pappalysin generally comprise a certain amount of Pappalysin covalently complexed and/or interacting non-covalently with stanniocalcin.
  • the level of free Pappalysin in a composition obtained as secreted Pappalysin is generally not known, because an unknown fraction of Pappalysin is bound by stanniocalcin polypeptides.
  • the present invention therefore in one aspect relates to a composition comprising Pappalysin, wherein said composition is essentially free of stanniocalcin.
  • the invention in another aspect relates to a method of producing a composition comprising Pappalysin polypeptide, wherein said composition is essentially devoid of stanniocalcin polypeptide, said method comprising removing stanniocalcin from a composition comprising Pappalysin.
  • the method comprises the steps of
  • Removal of stanniocalcin can include the removal of both free stanniocalcin polypeptide and/or stanniocalcin polypeptide interacting with other polypeptides, in particular stanniocalcin polypeptide interacting with Pappalysin polypeptide. It is preferred that both free stanniocalcins and complexed/interacting stanniocalcins are removed from the composition.
  • Stanniocalcin may be removed by any methods available to those of skill in the art.
  • the stanniocalcin polypeptides are removed by affinity chromatography; however other methods are also available and could be applied by those of skill in the art.
  • the invention includes monitoring the separation of PAPP-A and complexes of PAPP-A and stanniocalcin, regardless of the method used for the separation. Said monitoring includes the detection by methods described herein of PAPP-A and complexes of PAPP-A and stanniocalcin.
  • the invention also includes verification of separation by said methods.
  • composition comprising Pappalysin polypeptide is produced by the steps of
  • the cell line may be selected from any cell line, which expresses Pappalysin, preferably the cell line is a human cell line, such as a human cancer cell line.
  • stanniocalcin polypeptides may also be removed by deletion or disruption of one or more stanniocalcin genes in the cultured cell line.
  • Stanniocalcin may also be removed by knock-down, such as siRNA knockdown, such as knock-down of STC1 and/or STC2; preferably both STC1 and STC2 are knocked-down, deleted or disrupted.
  • knock-down such as siRNA knockdown, such as knock-down of STC1 and/or STC2; preferably both STC1 and STC2 are knocked-down, deleted or disrupted.
  • Techniques for gene knock-down, disruption and deletion/knockout are well known in the art.
  • the present invention provides a method of producing a composition comprising Pappalysin polypeptide, wherein said composition is essentially devoid of stanniocalcin polypeptide, said method comprising
  • the invention also relates in a separate aspect to a composition obtainable or obtained by the method of the invention for producing a composition comprising Pappalysin polypeptide, wherein said composition is essentially devoid of stanniocalcin polypeptide, said method being as defined above.
  • composition of the invention comprising Pappalysin, which composition is essentially free of stanniocalcin is of specific use in methods for quantifying the level/amount of Pappalysin in a sample.
  • the level of free Pappalysin can only be precisely determined, if a reference material is available with known concentration of Pappalysin, such as PAPP-A and/or PAPP-A2.
  • the composition of the present invention can be used as such a reference or standard material, because this composition is essentially free of stanniocalcin, and therefore, comprise only Pappalysin, which is not bound by stanniocalcin.
  • the present invention provides a method for quantifying the level of Pappalysin in a sample, said method comprising using a composition essentially free of stanniocalcin as a standard.
  • the composition is preferably a Pappalysin composition of the present invention, as defined herein above.
  • the method may comprise the steps of
  • the reference samples may comprise a negative control comprising no Pappalysin, and additional samples comprising any levels of Pappalysin, for example unbound
  • Pappalysin such as any level of Pappalysin between 0.1 ng/mL and 1000 ng/mL, such as approximately 0.1 ng/mL, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 400, 500, 600, 700, 800, 900 and/or 1000 ng/mL Pappalysin.
  • the present invention broadly relates to the use of stanniocalcin as regulators of Pappalysins.
  • the present inventors have found that stanniocalcin form stable non-covalent interactions and/or covalent complexes with Pappalysins.
  • interaction of stanniocalcins with Pappalysins serves to inhibit the proteolytic activity of Pappalysins.
  • stanniocalcins function as inhibitors of Pappalysins. This means that the activity of Pappalysins can be regulated via regulation of the interactions between stanniocalcins and Pappalysins.
  • the level of Pappalysin-stanniocalcin interactions can be increased by providing stanniocalcins, thereby promoting formation of Pappalysin-stanniocalcin interactions, and consequently inhibiting the activity of Pappalysin polypeptide.
  • the level of Pappalysin-stanniocalcin interactions can be decreased by providing an agent, which is capable of antagonizing interactions between Pappalysins and stanniocalcins, thereby increasing the level of unbound Pappalysin (Pappalysins not bound by stanniocalcins), which is catalytically active; i.e. thereby activating Pappalysin polypeptides.
  • the activity of Pappalysin polypeptide correlates negatively with the level of stanniocalcin and thus, the activity of Pappalysin polypeptide may be decreased by increasing the level of a stanniocalcin polypeptide, and increased by decreasing the level of a stanniocalcin polypeptide.
  • One embodiment of the present invention therefore relates to a method for decreasing or increasing the activity of a Pappalysin polypeptide, wherein
  • This method is preferably an in vitro method, where the Pappalysin activity is regulated in a sample, for example in a sample comprising a cell culture, such as a cell culture, which expresses one or more Pappalysin polypeptides.
  • the method is performed by increasing or decreasing the level of stanniocalcin polypeptide in a human cell, such as in a human stem cell.
  • the stanniocalcin polypeptide may be a stanniocalcin polypeptide derived from any species and thus can be any mammalian stanniocalcin polypeptide.
  • the stanniocalcin polypeptide is human or mouse STC1 or STC2.
  • the method can be applied to increase or decrease the level of a stanniocalcin polypeptide in a mammalian subject, such as a human being, such as in a specific tissue of a mammalian subject, such as a human being, for example a cancer tissue.
  • the present invention relates to a method of decreasing or increasing the activity of a Pappalysin polypeptide by decreasing or increasing the level of interacting Pappalysin and stanniocalcin polypeptides.
  • the level of a stanniocalcin polypeptide can be increased or decreased by providing or administering to the sample an agent capable of decreasing or increasing the level of stanniocalcin polypeptide and/or the level of interacting Pappalysin and stanniocalcin polypeptides is provided to a sample comprising said Pappalysin polypeptide.
  • agent capable of decreasing or increasing the level of stanniocalcin polypeptide and/or the level of interacting Pappalysin and stanniocalcin polypeptides is provided to a sample comprising said Pappalysin polypeptide.
  • agent capable of decreasing or increasing the level of stanniocalcin polypeptide and/or the level of interacting Pappalysin and stanniocalcin polypeptides is provided to a sample comprising said Pappalysin polypeptide.
  • the choice of agent depends on whether the activity of Pappalysin is intended to be increased or decreased.
  • a method for increasing the activity of a Pappalysin polypeptide by decreasing the level of free stanniocalcin polypeptide.
  • the activity of a Pappalysin polypeptide is increased by administering an agent, which antagonizes the interaction of stanniocalcin with Pappalysin.
  • Any antagonist, polypeptide, antibody, aptamer, small molecule or any other agent capable of binding stanniocalcin in a manner, which antagonizes its interaction with Pappalysin can be provided or administered in a method of the invention for increasing the activity of Pappalysin.
  • any antagonist, polypeptide, antibody, aptamer, small molecule or any other agent capable of binding Pappalysin in a manner, which antagonizes its interaction with stanniocalcin without affecting the activity of Pappalysin, or at least not significantly affecting the activity of Pappalysin can be provided or administered in the method.
  • the agent can be a stanniocalcin directed siRNA or an antibody, such as an antibody capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • an antibody such as an antibody capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • a method for inhibiting the activity of a Pappalysin polypeptide by providing or administering a stanniocalcin polypeptide.
  • stanniocalcin polypeptide there are many methods available to those of skill in the art to provide a stanniocalcin polypeptide.
  • stanniocalcin polypeptide could be provided in a suitable buffered solution, e.g. as a recombinant protein.
  • a suitable buffered solution e.g. as a recombinant protein.
  • stanniocalcin can be provided or administered also as stanniocalcin polypeptide in a suitable buffered solution.
  • a delivery system could be used, which involves transgene expression after transfection with a suitable vector, for example a recombinant mammalian expression vector or a viral vector, such as a retroviral vector.
  • a suitable vector for example a recombinant mammalian expression vector or a viral vector, such as a retroviral vector.
  • the stanniocalcin polypeptide could be provided using a nucleic acid vector expressing said stanniocalcin polypeptide or part thereof, for example using a retroviral vector.
  • the activity of Pappalysins has been implicated in a number of clinical conditions, specifically clinical conditions, which involves the regulation of proliferative processes.
  • the present invention provides methods for the prevention, treatment or amelioration of clinical condition, where the treatment involves either activation of Pappalysin, such as PAPP-A or inactivation of Pappalysin, such as PAPP-A.
  • Activation of Pappalysin is relevant for the treatment of clinical condition, where a stimulation of cellular proliferation is desired; such as in bone remodeling or bone growth and/or wound healing.
  • Inactivation or inhibition of Pappalysin is relevant for the treatment of clinical condition, where an inhibition of cellular proliferation is desired; such as in the treatment of cancers.
  • a method is provided of preventing, treating or ameliorating a clinical condition in a mammalian subject, such as a human being, said method comprising administering to said mammalian subject, such as a human being an effective amount of a stanniocalcin polypeptide.
  • the stanniocalcin polypeptide may be a stanniocalcin polypeptide derived from any species and thus can be any mammalian stanniocalcin polypeptide.
  • the stanniocalcin polypeptide is human or mouse STC1 or STC2.
  • stanniocalcin By providing stanniocalcin in an effective amount, the activity of a Pappalysin polypeptide can be inhibited.
  • the activity of said Pappalysin polypeptide is inhibited by interaction of a Pappalysin polypeptide with at least one stanniocalcin polypeptide, but native stanniocalcin polypeptides generally form dimers, and thus, Pappalysin is often inhibited by interaction with two stanniocalcin dimers.
  • stanniocalcin may also be used in the form of stanniocalcin monomers.
  • Stanniocalcin monomers can be produced by recombinant expression of stanniocalcin variants, having a deletion in one or more cysteine residues, thereby preventing formation of disulfide bridges between thiol groups of cysteine residues.
  • Pappalysin will be inhibited by interaction with stanniocalcin monomers, such as interaction with two stanniocalcin monomers.
  • an agent is provided or a pharmaceutical composition comprising such agent, which is capable of promoting interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide for use in medicine.
  • an agent could be an antibody capable of binding interacting Pappalysin and stanniocalcin polypeptides, as described elsewhere herein.
  • This method and use serves to inhibit proliferative processes, and thus, the method is preferably applied for prevention, treatment or amelioration of a proliferative disorder. It is preferred that the proliferative process is associated with Pappalysin expression, or is associated with increased expression of Pappalysin. Methods for determining the level of Pappalysin are described elsewhere herein. It is specifically relevant for proliferative processes and clinical conditions, which are characterized by increased level of Pappalysin.
  • the method is also specifically relevant for proliferative processes and/or proliferative disorders associated with Pappalysin-meditated cleavage of an Insulin-like growth factor-binding protein (IGFBP), in particular such proliferative processes and/or proliferative disorders associated with Pappalysin-meditated cleavage of IGFBP4.
  • IGFBP Insulin-like growth factor-binding protein
  • the clinical condition is a cancer; in particular any cancer type characterized by high level of Pappalysin, preferably characterized by high level of Pappalysin, which is not interacting with stanniocalcin polypeptide.
  • the clinical condition is a vascular disease, in particular atherosclerosis or restenosis.
  • the clinical condition is a condition of increased fluid accumulation, such as ascites production in ovarian cancer patients.
  • the clinical condition is a cancer selected from Acute Lymphoblastic Leukemia, Acute Myeloid Leukemia, Adrenocortical Carcinoma, AIDS-Related Cancers, AIDS-Related Lymphoma, Anal Cancer, Astrocytoma (e.g.
  • Ovarian Cancer Childhood Ovarian Cancer
  • Ovarian Epithelial Cancer Ovarian Germ Cell Tumor, Ovarian Low Malignant Potential Tumor, Pancreatic Cancer, Pancreatic Cancer, Paranasal Sinus and Nasal Cavity Cancer, Parathyroid Cancer, Penile Cancer, Pheochromocytoma, Pineoblastoma and Supratentohal Primitive Neuro-ectodermal Tumors, Pituitary Tumor, Pleuropulmonary Blastoma, Prostate Cancer, Renal Pelvis and Ureter Transitional Cell Cancer, Retinoblastoma, Rhabdomyosarcoma (such as Childhood Rhabdomyosarcoma), Salivary Gland Cancer, Adult-onset soft tissue Sarcoma, Soft Tissue Sarcoma (such as Childhood Soft Tissue Sarcoma), uterine Sarcoma, Sezary Syndrome, Skin Cancer (such as non-Melanoma skin cancer), Merkel Cell Skin Carcinoma, Small Intestine Cancer, Supratentorial Primitive
  • Neuroectodermal Tumors such as occurring in Childhood
  • Cutaneous T-Cell Lymphoma Testicular Cancer
  • Thymoma and Thymic Carcinoma Thyroid Cancer
  • Transitional Cell Cancer of the Renal Pelvis and Ureter Trophoblastic Tumor (such as Gestational Trophoblastic Tumor), Urethral Cancer, Endometrial uterine cancer, Uterine Sarcoma, Vaginal Cancer, Visual Pathway and Hypothalamic Glioma (such as Childhood Visual Pathway and Hypothalamic Glioma), Waldenstrom's Macro-globulinemia or Wilms' Tumor.
  • the cancer is selected from the group consisting of ovarian cancer, testicular cancer, lung cancer, or any cancer of the digestive system, including ventricular cancer, colon cancer, small bowel cancer and rectal cancer, in particular, the cancer is selected from the group consisting of ovarian cancer, lung cancer and colon cancer.
  • the cancer is ovarian cancer.
  • Other preferred clinical conditions include restenosis, atherosclerosis, ovulation, fibrosis, as well as clinical conditions related to human reproduction.
  • a mammalian subject such as a human being
  • said method comprising administering to said mammalian subject, such as a human being an effective amount of a stanniocalcin polypeptide
  • the stanniocalcin polypeptide can be administered by any suitable method available to those of skill in the art.
  • the stanniocalcin polypeptide is administered as stanniocalcin polypeptide in a suitable buffered solution adapted for therapeutic use.
  • a delivery system could be used, which involves transgene expression after transfection with a suitable vector, for example a recombinant mammalian expression vector or a viral vector, such as a retroviral vector.
  • a suitable vector for example a recombinant mammalian expression vector or a viral vector, such as a retroviral vector.
  • the stanniocalcin polypeptide could be provided using a nucleic acid vector expressing said stanniocalcin polypeptide or part thereof, for example using a retroviral vector.
  • the present invention also provides methods for treating clinical conditions, where an increase in cellular proliferation is desired.
  • Pappalysin is activated by inhibiting interaction between Pappalysins and stanniocalcins. This leads to more unbound Pappalysin, which is proteolytically active against for example IGFBP, such as IGFBP4, which stimulates the IGF-system.
  • the present invention pertains to a method of preventing, treating or ameliorating a clinical condition in a mammalian subject, such as a human being, said method comprising administering to said mammalian subject, such as said human being an effective amount of an agent capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • an agent capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • This method can be applied for stimulating a proliferative process, and thus, the method is applicable for clinical conditions such as bone fractures, where the treatment is bone remodeling and/or bone growth, and wounds, where the treatment or amelioration is wound healing.
  • the agent capable of decreasing the level of a stanniocalcin polypeptide is used in wound healing and/or bone remodeling or bone growth.
  • an agent is provided, or a pharmaceutical compostion comprising such agent, which agent is capable of antagonizing the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide for use in medicine.
  • Interactions between Pappalysin and stanniocalcin polypeptides can be inhibited by providing any agent capable of antagonizing interaction between Pappalysin and stanniocalcin.
  • agent includes for example, any antagonist, polypeptide, antibody, aptamer, small molecule or any other agent capable of binding stanniocalcin in a manner, which antagonizes its interaction with Pappalysin.
  • any antagonist, polypeptide, antibody, aptamer, small molecule or any other agent capable of binding Pappalysin in a manner, which antagonizes its interaction with stanniocalcin without affecting the activity of Pappalysin, or at least not significantly affecting the activity of Pappalysin, can be provided or administered in the methods of the invention.
  • the agent can be a stanniocalcin directed siRNA or an antibody, such as an antibody capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • an antibody such as an antibody capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • interactions between stanniocalcin and Pappalysin polypeptides are antagonized by providing an antibody, such as a blocking antibody, which inhibits the interaction of stanniocalcin with Pappalysin.
  • the clinical agents such as siRNA, antibodies and polypeptides, of the present invention herein may be administered by any suitable method available in the art.
  • the main routes of administration are parenteral injections, oral, and topical, as will be described below.
  • Other drug-administration methods such as subcutaneous injection, which are effective to deliver the drug to a target site or to introduce the drug into the bloodstream, are also contemplated.
  • intranasal administration and administration by pulmonary inhalation is convenient and effective methods of administration, which could be used.
  • the clinical agents may be administered orally, for example as an oral tablet. This is a convenient non-invasive approach for administration, which is also preferred by most patients. This administration can be used for agents, which are easily taken up via the gastrointestinal tract.
  • the clinical agents may be administered parenterally. This could also be relevant, where the agent is administered in combination with an additional agent, which requires parenteral injection.
  • the clinical agents provided herein are administered parenterally, that is by intravenous, intramuscular, subcutaneous, intranasal, intrarectal, intravaginal or intraperitoneal administration.
  • the intravenous forms of parenteral administration are generally preferred. Appropriate dosage forms for such administration may be prepared by conventional techniques.
  • the clinical agents may also be administered by inhalation that is by intranasal and oral inhalation administration.
  • the clinical agents of the present invention are delivered by intravenous, subcutaneous, and/or intra-muscular administration.
  • the dosage requirements will vary with the particular clinical agent employed, the route of administration and the particular individual being treated. Ideally, an individual to be treated by the present method will receive a pharmaceutically effective amount of the clinical agent in the maximum tolerated dose, generally no higher than that required before drug resistance develops.
  • a clinical agent such as siRNA, antibody or peptide
  • an effective amount herein is meant a dose that produces the therapeutic effects for which it is administered.
  • the exact dose will depend on the clinical condition or disorder to be treated, and can be ascertained by one skilled in the art using known techniques.
  • the an antibody or peptide of the present invention can be administered to a person in an amount of from 1 ⁇ g/kg to about 100 mg/kg per day.
  • an antibody or polypeptide of the invention can be administered in dosage ranges of 5 microgram to about 20 g per day.
  • suitable dosage ranges of antibody or polypeptide are typically 1-500 mg daily, preferably 1-100 mg daily, 70-200 mg daily, 70-150 mg daily and most preferably 1-30 mg daily, 30-70 mg daily, 40-60 mg daily, 45-55 mg daily or about 50 mg daily.
  • the suitable dose of antibody or polypeptide is 5-10 mg/kg bodyweight daily, or 10-20 mg/kg bodyweight, or even 20-25 mg/kg bodyweight or 25-30 mg/kg bodyweight or 30-40 mg/kg bodyweight or 40-50 mg/kg bodyweight or 50-60 mg/kg.
  • the clinical agents such as siRNA, antibody or polypeptide, as defined elsewhere herein is preferably administered at least once daily, and may therefore be administered once or twice daily.
  • the doses of clinical agent are preferably administered parenterally, for example by intraveneous injection.
  • the methods of the invention employ different regulatory agents capable of either increasing or decreasing the activity of Pappalysin by affecting the level of Pappalysin polypeptides, which is interacting with stanniocalcin polypeptides.
  • the agents thus employed in the methods as described elsewhere herein, are defined in the paragraph below.
  • agent is for example a stanniocalcin polypeptide or part thereof, an siRNA targeting stanniocalcin or an antibody of the invention.
  • the invention in a specific aspects relate to such regulatory agents.
  • the invention provides an agent capable of increasing or decreasing the level of a stanniocalcin polypeptide.
  • An agent capable of increasing the level of a stanniocalcin polypeptide includes any agent, which serves to increase the expression, stability, resistance to degradation etc. in respect of stanniocalcin.
  • the agent is a stanniocalcin polypeptide, such as STC1, STC2, or a variant or fragment thereof, which is capable of interacting with Pappalysin.
  • the stanniocalcin polypeptide is STC1 or STC2, such as human STC1 or STC2.
  • the agent capable of decreasing the level of a stanniocalcin polypeptide is used in the treatment of a restenosis, atherosclerosis, ovulation, fibrosis, or cancer, such as ovarian cancer, testicular cancer, lung cancer, or any cancer of the digestive system, including ventricular cancer, colon cancer, small bowel cancer and rectal cancer.
  • the invention relates to an agent capable of decreasing the level of a stanniocalcin polypeptide.
  • agent includes any agent, which inhibits expression and/or the stability of stanniocalcin.
  • the agent capable of decreasing the level of a stanniocalcin polypeptide is an siRNA targeting stanniocalcin, such as STC1 and/or STC2.
  • siRNA comprises or consists of a sequence of at least 5, such as at least 10, for example at least 15, for example at least 20 consecutive nucleotides selected from the STC1 or STC2 genes, such as the human STC1 gene identified by SEQ ID NO: 5 or the human STC2 gene identified by SEQ ID NO: 6.
  • the siRNA comprises or consists of a sequence of 5-30, such as 10-25, preferably 18-22 consecutive nucleotides selected from the STC1 or STC2 genes, such as the human STC1 gene identified by SEQ ID NO: 5 or the human STC2 gene identified by SEQ ID NO: 6.
  • STC1 or STC2 genes such as the human STC1 gene identified by SEQ ID NO: 5 or the human STC2 gene identified by SEQ ID NO: 6.
  • any interfering nucleic acid species can be used.
  • the invention relates to an agent capable of antagonizing the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • agent capable of antagonizing the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • agent includes any agent, which inhibits expression and/or the stability of stanniocalcin.
  • the agent capable of decreasing the level of a stanniocalcin polypeptide and/or capable of antagonizing the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide is used in wound healing and/or bone remodeling or bone growth.
  • An agent capable of antagonizing the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide may be selected from any antagonist, polypeptide, antibody, aptamer, small molecule or any other agent capable of binding stanniocalcin polypeptide in a manner, which antagonizes its interaction with Pappalysin. Also any antagonist, polypeptide, antibody, aptamer, small molecule or any other agent capable of binding Pappalysin in a manner, which antagonizes its interaction with stanniocalcin without affecting the activity of Pappalysin, or at least not significantly affecting the activity of Pappalysin polypeptide, is a relevant agent.
  • the agent is an antibody, as describes herein below.
  • the agent capable of antagonizing the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide is an antibody directed against a stanniocalcin polypeptide, such as an antibody specifically binding stanniocalcin polypeptide in a manner, which antagonize the interaction of stanniocalcin polypeptide with Pappalysin polypeptide.
  • the antibody is preferably directed against STC1 or STC2, such as human STC1 or STC2.
  • STC1 or STC2 such as human STC1 or STC2.
  • antibodies targeting both STC1 and STC2 are applicable.
  • the present inventors have identified C120 of STC2 to be involved in covalent binding of STC2 with pappalysin.
  • an antibody capable of antagonizing the interaction between STC and papplysin is directed against one or more peptides, which comprise the C120 residue of STC2.
  • an antibody is specific for a fragment of 3-15 amino acids selected from the region between amino acid residues 60 and 180 of STC2, such as a region between amino acid residues 70 and 170 of STC2, such as a region between amino acid residues 80 and 160 of STC2, such as a region between amino acid residues 90 and 150 of STC2, such as a region between amino acid residues 100 and 140 of STC2, such as a region between amino acid residues 110 and 130 of STC2, such as a region between amino acid residues 115 and 130 of STC2, such as a region between amino acid residues 119 and 125 of STC2,
  • candidate antibodies to specifically target stanniocalcin and antagonize its interaction with Pappalysin polypeptide can be verified by methods of the present invention.
  • antibodies targeting Pappalysin polypeptide can be relevant agents for antagonizing interactions between Pappalysin and stanniocalcin polypeptides.
  • the agent capable of antagonizing the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide is an antibody directed against a Pappalysin polypeptide, which antibody is capable of binding Pappalysin in a manner, which antagonizes its interaction with stanniocalcin without affecting the activity of Pappalysin, or at least not significantly affecting the activity of Pappalysin.
  • an antibody which is capable of specifically binding interacting stanniocalcin and Pappalysin polypeptides.
  • an antibody is provided, which is capable of promoting the interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide, for example by binding the Pappalysin polypeptide and/or a stanniocalcin polypeptide.
  • Pappalysin and stanniocalcin may interact covalently and/or non-covalently.
  • PAPP-A and stanniocalcin 1 interact non-covalently and PAPP-A and stanniocalcin 2 form a covalent complex.
  • an antibody of the invention is capable of specifically binding interacting stanniocalcin and Pappalysin polypeptides, such as a non-covalent interaction between PAPP-A and stanniocalcin 1 and/or a covalent complex between PAPP-A and stanniocalcin 2.
  • the antibody may simultaneously bind both interacting Pappalysin and stanniocalcin polypeptides; however, alternatively, the antibody may recognize a specific conformation of either Pappalysin or stanniocalcin polypeptide, which conformation is observed, when the polypeptides interact.
  • the antibody has a higher affinity for interacting Pappalysin and stanniocalcin polypeptides than either of Pappalysin or stanniocalcin individually.
  • Antibodies of the present invention can be raised by conventional methods by immunization of an animal. Such methods are also within the scope of the invention as is the selection of antibodies which arise from immunization.
  • the present invention relates to a method of producing an antibody specific for interacting Pappalysin and stanniocalcin polypeptides, said method comprising
  • the antibody can be produced in a method comprising the steps of
  • the Pappalysin and stanniocalcin polypeptides used for immunization may interact covalently or non-covalently, and in one embodiment, the interaction is a non-covalent interaction between PAPP-A or PAPP-A2 and STC1 and/or a covalent complex between PAPP-A or PAPP-A2 and STC2.
  • Recombinant Pappalysin and/or STC polypeptides can be used to generate antibodies.
  • Monoclonal antibodies reactive with Pappalysin and/or STC can be produced using standard techniques.
  • the present invention relates to a method of producing a monoclonal antibody specific for interacting Pappalysin and stanniocalcin polypeptides, which method comprises the steps of
  • Monospecific antibody as used herein is defined as a single antibody species or multiple antibody species with specific binding characteristics for Pappalysin and/or STC.
  • Specific binding as used herein refers to the ability of the antibody species to bind to a specific antigen or epitope, such as those associated with Pappalysin and/or STC, for example binding sites of STC for Pappalysin or binding sites of Pappalysin for STC.
  • Pappalysin and/or STC specific antibodies can generally be raised by immunizing animals such as mice, rats, guinea pigs, rabbits, goats, horses and the like, with rabbits or mice being preferred, with an appropriate concentration of Pappalysin and/or STC antigen either with or without an immune adjuvant.
  • immunizing animals such as mice, rats, guinea pigs, rabbits, goats, horses and the like, with rabbits or mice being preferred, with an appropriate concentration of Pappalysin and/or STC antigen either with or without an immune adjuvant.
  • antibodies specific against Pappalysin and/or STC can be used for the purification of native and recombinant Pappalysin and/or STC, as a laboratory reagent, and in antibody based diagnostic kits.
  • Monoclonal antibodies (mAb) reactive with Pappalysin and/or STC can be prepared by conventional methods, such as by immunizing inbred mice with Pappalysin and/or STC polypeptide/antigen.
  • the mice are immunized with about 0.1 mg to about 10 mg, preferably about 1 mg, of Pappalysin and/or STC polypeptide/antigen in about 0.5 ml buffer or saline incorporated in an equal volume of an acceptable adjuvant. Freund's complete adjuvant is preferred.
  • the mice receive an initial immunization on day 0 and are rested for about 3 to about 30 weeks.
  • Immunized mice may be given one or more booster immunizations of about 0.1 to about 10 mg of Pappalysin and/or STC polypeptide/antigen in a buffer solution such as phosphate buffered saline (PBS) by the intravenous (IV) route.
  • Lymphocytes from antibody-positive mice are obtained by removing spleens from immunized mice by standard procedures known in the art.
  • Hybridoma cells are produced by mixing the splenic lymphocytes with an appropriate fusion partner under conditions which will allow the formation of stable hybridomas.
  • Fused hybridoma cells are selected by growth in hypoxanthine, thymidine and aminopterin supplemented Dulbecco's Modified Eagles Medium (DMEM) by procedures known in the art.
  • Supernatant fluids are collected form growth positive wells on about days 14, 18, and 21 and are screened for antibody production by an immunoassay such as solid phase immunoradioassay (SPIRA) using Pappalysin and/or STC as the antigen.
  • SPIRA solid phase immunoradioassay
  • the culture fluids are also tested in the Ouchterlony precipitation assay to determine the isotype of the mAb.
  • Hybridoma cells from antibody positive wells are then cloned.
  • In vitro production of anti-Pappalysin or anti-STC is carried out by growing the hybridoma in culture medium to obtain sufficient quantities of the specific mAb.
  • the mAb are purified by techniques known in the art.
  • Antibody titers of ascites or hybridoma culture fluids are determined by various serological or immunological assays which include, but are not limited to, precipitation, passive agglutination, enzyme-linked immunosorbent antibody (ELISA) technique.
  • ELISA enzyme-linked immunosorbent antibody
  • the “monoclonal antibodies” may also be isolated from phage antibody libraries. Identified phage antibodies can be produced by expression in bacteria.
  • Methods such as those described above may be used to produce monospecific antibodies specific for Pappalysin and/or STC polypeptide fragments or full-length nascent Pappalysin and/or STC polypeptide.
  • Pappalysin and/or STC antibody affinity columns can be made by adding the antibodies to a gel support, such as Affigel-10 (Biorad), a gel support which is pre-activated with N-hydroxysuccinimide esters such that the antibodies form covalent linkages with the agarose gel bead support.
  • the antibodies are then coupled to the gel via amide bonds with the spacer arm.
  • the remaining activated esters are then quenched with 1M ethanolamine HCl (pH 8).
  • the column is washed with water followed by 0.23 M glycine HCl (pH 2.6) to remove any non-conjugated antibody or extraneous protein.
  • the column is then equilibrated in phosphate buffered saline (pH 7.3) and the cell culture supernatants or cell extracts containing Pappalysin and/or STC or Pappalysin and/or STC fragments are slowly passed through the column.
  • the column is then washed, and the protein is eluted.
  • the purified Pappalysin and/or STC protein is then dialyzed against phosphate buffered saline.
  • Native Pappalysin and/or STC from sources such as human plasma or serum, tissue extracts, or media from nontransfected cell lines (that endogenously secrete STC) may also be purified by use of an antibody affinity column.
  • kits based on antibodies may be used for diagnostic purposes.
  • the assays include, but are not limited to, precipitation, passive agglutination, enzyme-linked immunosorbent assay (ELISA) techniques, and radioimmunoassay (RIA) techniques.
  • a sandwich assay can be constructed where antigen present in an sample is caught by immobilized monoclonal or polyclonal anti(STC). Detection is then performed by the use of one or more monoclonal Pappalysin antibodies and peroxidase conjugated anti(murine IgG). In another assay, antigen present in an sample is caught by immobilized monoclonal or polyclonal anti(Pappalysin), and detected using biotinylated polyclonal anti(STC).
  • ELISA sandwich assay can also be constructed where any antigen present in sample is caught by immobilized monoclonal antibody. Detection is then performed by the use of a conjugated monoclonal antibody, such as biotinylated antibody.
  • a conjugated monoclonal antibody such as biotinylated antibody.
  • interacting Pappalysin and stanniocalcin polypeptides are detected contacting the sample with a monoclonal antibody specifically binding covalent and/or non-covalent complexes of Pappalysin and stanniocalcin, followed by detection by contacting the Pappalysin/stanniocalcin-antibody complex with a conjugated monoclonal antibodies, such as biotinylated antibody.
  • Assays can be calibrated using purified Pappalysin and/or STC, in particular using a composition comprising a known concentration of unbound Pappalysin or a known concentration of interacting Pappalysin and STC polypeptides. Such calibration may involve constructing a standard curve by serial dilution.
  • Polyclonal and/or monoclonal antibodies may be used to inhibit the interaction of STC with Pappalysin, in a preferred embodiment, however, monoclonal antibodies are used.
  • Such antibodies are also called blocking antibodies herein.
  • such antibodies can be used to inhibit a non-covalent interaction between PAPP-A and STC1 and/or formation of a covalent complex comprising or consisting of PAPP-A and STC2, and/or a non-covalent interaction between PAPP-A2 and STC1 and/or formation of a covalent complex comprising or consisting of PAPP-A2 and STC2.
  • Certain monoclonal antibodies may also be inhibitory towards the interaction of STC with Pappalysin. Such monoclonal antibodies are likely to recognize an epitope in the binding site for Pappalysin, but the inhibitory activity may also be based on binding to neighbouring epitopes. Inhibitory monoclonal antibodies can be obtained by immunization with Pappalysin and/or STC polypeptides or fragments thereof.
  • IGF-BP such as IGF-BP4
  • an antibody capable of inhibiting STC binding to Pappalysin also serves to activate or promote Pappalysin-mediated cleavage of IGF-BP4, which then leads to activation of IGF receptor.
  • Activation of IGF receptor is known to be involved in cellular proliferation and is also known to be associated with atherosclerotic plaques.
  • Antibodies which are inhibitory towards the interaction between Pappalysin and STC have therapeutic value in clinical conditions in which it is be desirable to increase the activity of Pappalysin.
  • Such conditions include for example wound healing and bone remodelling as described herein above.
  • the invention in one aspect pertains to a method of determining a clinical condition, said method comprising detecting interacting Pappalysin and stanniocalcin polypeptides.
  • the method comprises detecting a Pappalysin polypeptide, which interacts with a stanniocalcin polypeptide.
  • a stanniocalcin polypeptide is detected, which interacts with a Pappalysin polypeptide.
  • any specific Pappalysin/stanniocalcin interaction may be detected in the diagnostic method.
  • the interaction may include both non-covalent interactions and covalent complexes.
  • the interaction is a non-covalent interaction between PAPP-A and STC1 and/or STC2.
  • the interaction is a non-covalent interaction between PAPP-A2 and STC1 and/or STC2.
  • the interaction is a covalent complex between PAPP-A and STC1 and/or STC2; and in yet another embodiment, the interaction is a covalent complex between PAPP-A2 and STC1 and/or STC2.
  • the interaction is a non-covalent interaction between PAPP-A and stanniocalcin 1.
  • the interaction is a covalent complex between PAPP-A and stanniocalcin 2.
  • the diagnostic method may be used for the determination of any relevant clinical condition; in particular such conditions, which are associated with Pappalysin and/or stanniocalcin.
  • the clinical condition is a cancer.
  • the clinical condition is a cancer selected from Acute Lymphoblastic Leukemia, Acute Myeloid Leukemia, Adrenocortical Carcinoma, AIDS-Related Cancers, AIDS-Related Lymphoma, Anal Cancer, Astrocytoma (e.g.
  • the cancer is selected from the group consisting of ovarian cancer, testicular cancer, lung cancer, or any cancer of the digestive system, including ventricular cancer, colon cancer, small bowel cancer and rectal cancer, in particular, the cancer is selected from the group consisting of ovarian cancer, lung cancer and colon cancer.
  • the cancer is ovarian cancer.
  • Other preferred clinical conditions include restenosis, atherosclerosis, ovulation, fibrosis, as well as clinical conditions related to human reproduction.
  • the interacting Pappalysin and stanniocalcin polypeptides may be detected using any suitable method, in particular any method of the present invention, as defined elsewhere herein.
  • interaction between Pappalysin and stanniocalcin is detected using at least one antibody.
  • the interaction is preferably detected using two different antibodies in a solid phase immunoassay, such as ELISA.
  • the interaction may be detected using a Pappalysin-specific antibody and/or a stanniocalcin-specific antibody.
  • a Pappalysin-specific antibody can be used as a catching antibody and then a stanniocalcin-specific antibody can be used as detecting antibody.
  • the function of the antibodies can be reciprocated, and a stanniocalcin-specific antibody can be used as a catching antibody and a Pappalysin-specific antibody as detecting antibody.
  • a main aspect of the present invention relates to interacting Pappalysin and stanniocalcin polypeptides. Such interacting polypeptides are of use in a number of different applications, which are also within the scope of the present invention. Therefore, certain aspects of the present invention relates to the use of Pappalysin/stanniocalcin interactions or complexes in methods for identifying specific agents, which can be used in the detection and/or regulation of interacting Pappalysin and stanniocalcin polypeptides; in particular in detection and/or regulation of a non-covalent interaction between PAPP-A and stanniocalcin 1 and/or a covalent complex between PAPP-A and stanniocalcin 2.
  • Potential detecting agents or regulating/modulating agents of interacting Pappalysin and stanniocalcin polypeptides may include any relevant agent, such as any agent with therapeutic potential.
  • the agent is an antibody, such as an antibody directed against an epitope of a Pappalysin or stanniocalcin polypeptide or part thereof.
  • a method is provided of identifying an agent capable of antagonizing interaction of a stanniocalcin polypeptide with a Pappalysin polypeptide.
  • antistanniocalcin in relation to the interaction between stanniocalcin and Pappalysin generally refers to the ability of the agent to inhibit interaction between Pappalysin and stanniocalcin.
  • the method of the invention comprises the steps of
  • a collection of Pappalysin directed agents such as anti-Pappalysin antibodies, can be screened for the ability to bind Pappalysin in a manner, which antagonize the interaction of Pappalysin with stanniocalcin.
  • a collection of stanniocalcin directed agents, such as anti-stanniocalcin antibodies can be screened for the ability to bind stanniocalcin in a manner, which antagonize the interaction of stanniocalcin with Pappalysin.
  • an agent is identified, which is capable of binding interacting Pappalysin and stanniocalcin polypeptides, by a method comprising
  • an agent is identified, which is capable of binding a polypeptide region of a Pappalysin or stanniocalcin polypeptide, which region is not surface exposed in interacting Pappalysin and stanniocalcin polypeptides, by a method comprising
  • an agent is identified, which is capable of binding a unbound Pappalysin polypeptide (i.e. Pappalysin, which do not interact with a stanniocalcin polypeptide), wherein said agent binds Pappalysin in a region comprising the binding site for stanniocalcin, by a method comprising
  • an agent is identified, which is capable of binding unbound stanniocalcin polypeptide (i.e. stanniocalcin, which do not interact with a Pappalysin polypeptide), by a method comprising
  • pools of agents, such as antibodies, specifically binding either Pappalysin and/or stanniocalcin can be screened for their ability to selectively bind interacting Pappalysin/stanniocalcin polypeptides, without binding non-interacting Pappalysin or stanniocalcin polypeptides
  • HEK293T Human embryonic kidney 293T cells (DuBridge 1987) were maintained in high-glucose Dulbecco's modified eagles medium (DMEM) supplemented with 10% fetal bovine serum, 2 mM glutamine, nonessential amino acids, and gentamicin (10% SEM).
  • DMEM Dulbecco's modified eagles medium
  • transient transfection 2.5*10 6 cells were plated onto 6 cm culture dishes or 6,3*10 6 cells were plated onto 10 cm culture dishes and transfected 20 hours later (at a cell confluence of 60-70%) by calcium phosphate co-precipitation using 10 or 20 ⁇ g plasmid DNA, respectively, prepared by GenElute HP Plasmid Miniprep Kit (SIGMA) or Plasmid Giga Kit (QIAGEN) eluted in 2 mM Tris, pH 7.4. Transfected cells were maintained in 10% SEM or serum free medium (SFM). Harvested culture medium was cleared by centrifugation (3 min, 3200 rpm), and the culture supernatant was saved.
  • SIGMA GenElute HP Plasmid Miniprep Kit
  • QIAGEN Plasmid Giga Kit
  • Angiotensinogen (AGT) cDNA pcDNA3.1-AGT
  • PAPP-A variants Constructs containing cDNA encoding PAPP-A variants were described previously; PAPP-A-E483Q (Boldt 2001), PAPP-AdLNR1, PAPP-AdLNR2, PAPP-AdLNR1-2, PAPP-A-356A, PAPP-A389A (Weyer 2007), PAPP-A/PAPP-A2 chimeras (E. Gaidamauskus, C. Oxvig, unpublished), zfPAPP-A (Kjr-Sorensen 2009, unpublished), muPAPP-A (Soe 2002)
  • Human STC1 cDNA pcDNA3.1-STC1 encoding C-terminally myc-his-tagged human STC1 (made by J. Mikkelsen, C. Oxvig, unpublished)
  • Human STC2 cDNA pcDNA3.1-STC2 encoding C-terminally myc-his-tagged human STC2 (made by J. Mikkelsen, C. Oxvig, unpublished)
  • proMBP cDNA pcDNA3.1-proMBP was made previously (Overgaard 2004).
  • Samples were non-reduced or reduced by the addition of dithiothreitol (DTT). Samples were afterwards added to Laemmli loading buffer and heated for two minutes at 100° C. before loading on 5-15%, 10-20%, or 12% Tris-glycine gels. The gels were run for 40-60 minutes at 30 mA in Laemmli buffer in Sodium Dodecyl Sulfate-Polyacrylamide Gel Electrophoresis. Proteins were visualized by Coomassie Brilliant Blue staining or Western blotting. Radiolabeled proteins were visualized by autoradiography using a Typhoon Phosphorimager.
  • DTT dithiothreitol
  • PVDF polyvinylidene difluoride
  • HRP horse radish peroxidase
  • 293T cells were co-transfected with 5 ⁇ g PAPP-A and 5 ⁇ g empty plasmid DNA (for comparison), 5 ⁇ g STC1 or 5 ⁇ g STC2 cDNA.
  • STC1 and STC2 cells were co-transfected with 5 ⁇ g PAPP-A, 2.5 ⁇ g STC1 and 2.5 ⁇ g STC2 cDNA. Compared cells were always transfected with equal amounts of DNA.
  • the culture supernatants were afterwards analyzed by Western blotting using polyclonal antibodies detecting PAPP-A/proMBP (effectively polyclonal PAPP-A antibodies) or polyclonal antibodies detecting human STC1 or STC2.
  • culture supernatants containing recombinant PAPP-A or PAPP-A-E389Q and STC1 or STC2 were mixed in a 1:1 volume.
  • purified protein was first mixed with medium from mock-transfected cells (to obtain a 10 ⁇ g/mL concentration of PAPP-A/proMBP), and then mixed with STC2-medium, 1:1. Mixtures were incubated at 37° C. ON or samples were taken out at defined timepoints and frozen to stop complex formation. To visualize formed complexes, the mixtures were analyzed by the complex specific ELISA or Western blotting using polyclonal antibodies detecting PAPP-A/proMBP or polyclonal antibodies detecting STC1 or STC2.
  • 293T cells were transiently transfected with STC1 or STC2 cDNA (20 ug plasmid DNA per 10 cm plate) by calcium phosphate co-precipitation as explained in section 7.1.1. 48 hours post-transfection, 10% SEM was changed to serum-free medium (SFM), which was harvested and replaced two days later by fresh SFM, which was harvested after an additional two days.
  • SFM serum-free medium
  • SFM containing recombinant human STC1 or STC2 was mixed 1:1 with binding buffer (20 mM imidazole, 50 mM NaH 2 PO 4 , 1 M NaCl, 0.05% Tween-20, pH 7.5) and sterile filtrated before loading onto affinity columns.
  • Columns were packed with Chelating Sepharose Fast Flow affinity media (GE Healthcare), which was charged with Ni 2+ by addition of 2% NiSO 4 in H 2 O and equilibrated in binding buffer. Sample solutions were added to the columns at a flow rate of 1 mL/minute ON. Columns were afterwards washed with binding buffer, and proteins were eluted in 10 fractions of 250 ⁇ L elution buffer (50 mM NaH 2 PO 4 , 300 mM imidazole, pH 7.5).
  • PAPP-A Proteolytic Assay PAPP-A was pre-incubated with mock-, STC1- or STC2-medium in a 1:1 volume at 37 ° C. ON. PAPP-A samples (200x diluted) were incubated at 37° C. with purified, 125 I-labeled IGFBP-4 (pre-incubated with IGF-II, 50 nM, 0.35 ⁇ g/mL) or IGFBP-5 (10 nM, 0.30 ⁇ g/mL) in 50 mM Tris, 100 mM sodium chloride, 1 mM calcium chloride, pH 7.5.
  • STC1 and STC2 in the conditioned media were detected both under reducing and non-reducing conditions.
  • STC1 was detected in a faint band of ⁇ 70 kDa, representing the covalently linked STC1 dimer ( FIG. 1A ).
  • Loading a larger amount of sample lead to a much more distinct band.
  • one STC1 band of ⁇ 35 kDa appeared, corresponding to the STC1 monomer.
  • the STC2 monomer also appeared under reducing conditions, and was represented by a distinct band of ⁇ 45 kDa ( FIG. 1B ).
  • STC2 protein was primarily represented by bands of ⁇ 100 kDa, but bands of higher molecular weights of ⁇ 200 kDa as well as ⁇ 150 kDa and >250 kDa were also detectable. These bands probably represented multimers of STC2 protein. In general, the STC-detecting antibodies seemed to recognize reduced STC better than non-reduced protein.
  • proMBP is a well-known inhibitor of PAPP-A. Formation of the PAPP-A/proMBP complex has previously been shown to occur outside of cells when culture supernatants containing separately synthesized recombinant proMBP and PAPP-A were mixed. In a similar experiment, it was examined if the formation of the PAPP-A/STC2 complex was possible in the absence of cells. 293T cells were transfected with empty plasmid DNA (mock), PAPP-A or STC2 cDNA. Culture supernatant from the PAPP-A-transfected cells was mixed in a 1:1 volume with either STC2- or mock-medium and incubated at 37° C. Samples were taken out at defined time points. After incubation, PAPP-A Western blots were made to examine the appearance of HMW PAPP-A bands ( FIG. 3 ).
  • the data show, that a complex comprising or consisting of recombinant PAPP-A and STC2 can be formed upon co-transfection and by mixing of separately synthesized PAPP-A and STC2 protein. Furthermore, it is likely, that the HMW bands of PAPP-A observed in Western blotting of PAPP-A samples represent complexes of PAPP-A and endogenous STC2. Even though a covalent complex between PAPP-A and STC1 could not be detected, the existence of a non-covalent PAPP-A/STC1 complex is also likely.
  • STC2 was detected in medium containing recombinant PAPP-A and in a sample of purified PAPP-A-E483Q. In both cases, STC2 was detected in the HMW- complex, suggesting that it was complexed to PAPP-A. STC2 was, however, not detected in a sample of purified PAPP-A/proMBP complex.
  • STC1 and STC2 protein was therefore purified from serum-free medium of 293T cells transfected with STC1 or STC2 cDNA, respectively.
  • the STC proteins were purified by immobilized Ni 2+ affinity chromatography. Purified STC1 and STC2 protein was visualized in coomassie brilliant blue stained SDS-PAGE of eluted protein fractions ( FIG. 5 ).
  • Purified protein was visible in fractions #2-6. As in the STC1 Western blots, purified STC1 migrated primarily in a band of ⁇ 70 kDa ( FIG. 5A ). Furthermore, as expected from the STC2 Western blots, purified STC2 migrated in bands of multiple sizes, the primary one being of ⁇ 100 kDa ( FIG. 5B ). The appearance of HMW STC2 bands of >170 kDa could indicate formation of STC2-multimers or complex formation with unidentified proteins. Thus, since several bands were observed, especially for STC2, the identity of proteins in bands appearing under reducing and non-reducing conditions was investigated.
  • PAPP-A proteolytic activity of PAPP-A was affected by complex formation with the STCs.
  • PAPP-A was pre-incubated with mock-medium or medium containing recombinant STC1 or STC2.
  • PAPP-A/STC2 complex formation was verified by Western blotting.
  • the proteolytic activity of PAPP-A and PAPP-A/STC was monitored using 125 1-IGFBP-4 pre-incubated with IGF-II as described previously.
  • PAPP-A mediated proteolytic cleavage of IGFBP-4 at different time points was determined by correlating the intensities of bands representing intact and cleaved IGFBP-4, separated by SDS-PAGE ( FIG. 6A ).
  • Proteolytic cleavage assays and kinetic analyses were carried out with 125I-labeled natural substrate (IGFBP-4). Cleavage products were separated from intact substrate by SDS-PAGE, and cleavage was analyzed by photostimulated luminescence. Protein interaction studies and circular dichroism analysis were done using purified recombinant proteins. Assessment of protein concentrations were performed by quantitative amino acid analysis or by using immunoassays.
  • mice expressing STC2 or STC2(C120A) were generated using a ubiquitously strong promoter. Growth of mice was monitored by consecutive weighing.
  • Plasmid DNA containing the coding sequence of human STC1 (nt. 285-1025 of NM_003155.2 flanked by a 5′ XhoI site and a 3′ Hindi!l site) and STC2 (nt. 1131-2216 of NM_003714.2 flanked by a 5′ XhoI site and a 3′ Hindi!l site) were purchased (Invitrogen).
  • the cDNAs were cloned into the XhoI/HindIII sites of pcDNA3.1/Myc-His( ⁇ ) A (Invitrogen) to obtain pSTC1 and pSTC2.
  • cDNA was synthesized from mouse placental mRNA using two specific primers (5′-CCGAGAGGTCAGGAGAGCAG-3′ (nt. 3120-3101) and 5′-GAGCTTCTCTTTTAGTCTGCCCCC-3′ (nt. 5425-5402). Two overlapping PCR fragments, both containing the Bglll site at nt.
  • 2957 were generated using two sets of primers (5′-CCGGGGTACCATGATGTGTTGGAAGGTCCTGAG-3′ (nt. 1-23, Kpnl underlined) and 5′-GATGGTGAGCGGTATGTCACAA-3′ (nt. 3030-3009); 5′-CCGGTCCAGGCGGATACCCT-3′ (nt. 2881-2900) and 5′-GATCTCTAGATTACTGGTTTTCTTCTGCCTTGGGG-3′ (nt. 5370-5346, Xbal underlined)).
  • the fragments were ligated and cloned into the Kpnl/Xbal sites of pcDNA3.1(+) (Invitrogen) to generate pmPAPP-A2.
  • Mutagenesis of pSTC2 was carried out by QuikChange (Stratagene) using pSTC2 as a template, and the following sets of primers (numbering of NM_003714.2, mutated nucleotides underlined): 5′-GCACAGGTTCGGCGCCATAAGCCGGAAGTG-3′ (nt. 1655-1684) and 5′-CACTTCCGGCTTATGGCGCCGAACCTGTGC-3′ (nt.
  • Human embryonic kidney 293T cells (293tsA1609neo) were maintained in high-glucose DMEM supplemented with 10% fetal bovine serum, 2 mM glutamine, nonessential amino acids, and gentamicin (Invitrogen).
  • DMEM high-glucose DMEM supplemented with 10% fetal bovine serum, 2 mM glutamine, nonessential amino acids, and gentamicin (Invitrogen).
  • 6.0 ⁇ 10 6 cells were plated onto 10-cm dishes and transfected 18 h later by calcium phosphate coprecipitation using 5-10 ⁇ g plasmid DNA prepared by GenElute HP Plasmid Miniprep Kit (Sigma). Culture supernatants were harvested 48 h post transfection and cleared by centrifugation, or the cells were further cultured in serum free medium (CD293, Invitrogen) to facilitate purification.
  • Secreted levels of PAPP-A were determined by a commercial ELISA (AL-101, Ansh
  • His-tagged recombinant proteins was carried out by affinity chromatography on a 1 ml HisTrap HP column (GE Healthcare). Serum-free media were diluted 1:1 in 20 mM NaH2PO4, 150 mM NaCl, pH 7.4 (PBS) and loaded onto the column with a flow rate of 1 ml min ⁇ 1 . The column was washed with 20 column volumes of 50 mM NaH 2 PO 4 , 1 M NaCl, 20 mM imidazole, 0.05% Tween-20, pH 7.4, followed by five column volumes of PBS.
  • the proteins were eluted with 50 mM NaH 2 PO 4 , 300 mM imidazole, pH 7.4, and dialyzed against 20 mM HEPES, 150 mM NaCl, pH 7.4. Prior to iodination, IGFBP-4 and -5 were further purified by reversed-phase high pressure liquid chromatography (RP-HPLC) on a Discovery BIO Wde Pore C5 column (4 ⁇ 250 mm, Sigma), as described. Protein purity was assessed by SDS-PAGE, and quantification of purified proteins was done by amino acid analysis.
  • RP-HPLC reversed-phase high pressure liquid chromatography
  • IGFBP-4 was labeled with 125 1 (Amersham Biosciences), and cleavage reactions were carried out as previously described.
  • media harvested from cells transfected with human PAPP-A cDNA with or without pSTC1, pSTC2, or pSTC2(C120A) were diluted (1:500) to 50 ⁇ M PAPP-A and mixed with preincubated 125 I-IGFBP-4 (10 nM) and IGF-II (100 nM) (GroPep Bioreagents) in 50 mM Tris-HCl, 100 mM NaCl, 1 mM CaCl2, pH 7.5.
  • Cleavage of 125 I-IGFBP-5 was assessed similarly for the following proteinases with or without a 10-fold molar excess of purified STC1 or STC2: Human MMP-2 (R&D Systems, 902-MP-010), human ADAM-10 (R&D Systems, 936-AD-020), human matriptase, bovine trypsin (Sigma, T-8642), and human or murine PAPP-A2. Enzyme concentrations were 100 nM, except for trypsin (0.2 nM) and PAPP-A2 (50 ⁇ M). STC2 was preincubated with all proteinases for 8 h. Cleavage reactions were 30-180 min, to obtain approximately 30% substrate cleavage.
  • mice For use in ELISA and for immunoprecipitation, monoclonal antibodies against STC2 were raised.
  • Initial injections of 50 ⁇ g of purified recombinant human STC2 was given to BALB/c mice subcutaneously in Freund's Complete Adjuvant (MP Biomedicals).
  • a booster injection in Freund's Incomplete Adjuvant (MP Biomedicals) was given after one month.
  • responders were selected for final boosting one month after the first booster injection.
  • mice received intraperitoneal injections of 160 ⁇ g STC2. On the fifth day, the mice were sacrificed and the spleens removed. Spleen cells were centrifuged, aliquoted and stored in liquid nitrogen.
  • Fusion with SP2/0 cells was performed with one aliquot of the spleen cells.
  • Culture supernatants of picked clones were screened on STC2 coated plates, and positive clones were re-cloned. Resulting clones were STC216, STC220, STC221, STC225, STC239, and STC243.
  • the clones were cultured in CD Hybridoma Medium (Invitrogen) for antibody production.
  • Antibodies were purified on protein A Sepharose (GE Healthcare), and dialyzed against 20 mM HEPES, 150 mM NaCl, pH 7.5.
  • mAb STC216 was incubated at 7.4 ⁇ M with a 20-fold molar excess of EZ-Link Sulfo-NHS-LC-Biotin (Thermo Fisher Scientific, #21335) on ice for 2 h. The reaction was stopped with 10 mM Tris-HCl, and dialyzed against 20 mM HEPES, 150 mM NaCl, pH 7.5.
  • 96-well plates (MaxiSorp, Nunc) were coated with 100 ⁇ l per well of 7.5 ⁇ g ml ⁇ 1 of catching antibody (mAb STC221) in 100 mM Na 2 HCO 3 , pH 9.4 by overnight incubation at 4° C. The wells were then blocked with 200 ⁇ l per well of 2% bovine serum albumin (BSA) in TBS (30 mM Tris-HCl, 300 mM NaCl, 2 mM CaCl2, pH 7.4) for 30 min at 37° C.
  • BSA bovine serum albumin
  • Samples were diluted in TBS-T (TBS containing 0.05% Tween-20) supplemented with 1% BSA and incubated in the coated wells for 1 h at 37° C. Following washing in TBS-T, the wells were incubated for 1 h at 37° C. with biotinylated detecting antibody (STC216) diluted in TBS-T with 1% BSA to 1 ⁇ g ml ⁇ 1 , washed again, and incubated (1 h) with avidin-conjugated horseradish peroxidase (P0347, DAKO) diluted 1:20,000 in TBS-T with 1% BSA.
  • TBS-T TBS containing 0.05% Tween-20
  • Proteins separated by SDS-PAGE were blotted onto a PVDF membrane (Millipore), blocked with 2% Tween 20, and equilibrated in 50 mM Tris-HCl, 500 mM NaCl, 0.1% Tween 20, pH 9.0 (TST).
  • Primary antibodies were diluted (to 1-5 ⁇ g ml ⁇ 1 ) in TST containing 0.5% fetal bovine serum, and blots were incubated overnight at room temperature.
  • the blots were incubated for 1 h at room temperature with secondary antibodies (polyclonal swine anti-rabbit IgG-HRP (DAKO, P0217), polyclonal rabbit anti-goat IgG-HRP (DAKO, P0160), or polyclonal rabbit anti-mouse IgG-HRP (DAKO, P0260)) diluted 1:2000 in TST containing 0.5% fetal bovine serum. All washing between the steps was carried out with TST.
  • the blots were developed using enhanced chemiluminescence (ECL Prime, GE Healthcare), and images were captured and analyzed using an ImageQuant LAS 4000 instrument (GE Healthcare).
  • culture media were incubated 0-16 h at 37° C., separated by nonreducing SDS-PAGE (2 ⁇ l per lane), and then analyzed by Western blotting as described above. Media from cotransfected cells were not incubated prior to analysis.
  • Binding analysis was performed at 25° C., and data were collected at a rate of 10 Hz. Recorded signals were subtracted the background signal, as determined by the response obtained from the reference cell. Global fitting of a 1:1 Langmuir model was performed, using the Biacore T200 Evaluation Software, version 1.0.
  • Purified wild-type and mutant proteins were compared by using circular dichroism analysis. Prior to analysis, purified proteins were dialyzed against 20 mM NaH2PO4, 20 mM NaF, pH 7.4. Ten CD spectra were recorded at 25° C. for each protein on a Jasco J-810 spectropolarimeter (Jasco Spectroscopic, Japan) using a polypeptide concentration of 0.5 mg ml ⁇ 1 and a cuvette of 2 mm path length. CD data were obtained in the range from 260 to 190 nm at a resolution of 0.2 nm using a bandwidth of 1.0 nm. The scan speed was 100 nm min ⁇ 1 , and the response time was 1 s.
  • Temperature scans were carried out in the range from 260 to 200 nm, and melting curves were recorded at 222 nM. As (expressed in deg cm 2 dmol ⁇ 1 ) were calculated on the basis of a mean molar mass of 110 g mol ⁇ ' residue ⁇ 1 .
  • PAPP-A was then added and cleavage reactions were carried out in the same buffer for 20 min at 37° C. Prior to use, PAPP-A was incubated with or without STC1, STC2, or STC2(C120A) in serum medium for 16 h at 37° C. The stimulated cells were lysed on ice with RIPA buffer (Sigma, R0278), supplemented with Proteinase Inhibitor Cocktail (Sigma, P8340) and Phosphatase Inhibitor Cocktail Set II (EMD Millipore, 524625), for 10 min.
  • RIPA buffer Sigma, R0278
  • Proteinase Inhibitor Cocktail Sigma, P8340
  • Phosphatase Inhibitor Cocktail Set II EMD Millipore, 524625
  • PCR fragments encoding untagged STC2 or STC2(C120A) were generated by using the primers 5′-CGCAAATGGGCGGTAGGCGTG-3′ (nt. 769-789 of pcDNA3.1-Myc-His( ⁇ )A) and 5′-AAAAAAAGATCTTCACCTCCGGATATCAGAATACTC-3′ (nt. 2219-2196 of NM_003714.2, Bglll site underlined), and pSTC2 and pSTC2(C120A), respectively, as templates.
  • PCR fragments were cloned into the XhoI/Bglll sites of pCAGGS (BCCM, LM BP 2453) to generate pCAGGS-STC2 and pCAGGS-STC2(C120A). Plasmid DNA was linearized with Pvul, and microinjected into male pronuclei of
  • B6D2F2 zygotes (Taconic), which were then introduced into pseudopregnant NMRI female mice (Taconic).
  • Transgenic mice, B6D2F2-Tg(STC2), or B6D2F2-Tg(STC2(C120A)) were identified by PCR using pCAGGS plasmid-specific primers (5′-CGGAAGGACATATGGGAGGGCAAATC-3′ (nt. 216-241), and 5′-TGACTGGGAGTAGTCAGGAGAGGAGG-3′ (nt. 511-486), and genomic DNA purified from tail biopsies. Of 44 mice resulting from pCAGGS-STC2-injections, nine were positive for the transgenic insert.
  • mice resulting from pCAGGS-STC2(C120A)-injections nine were positive. Three of these gave rise to transgenic offspring with detectable levels of STC2 in the serum, and were used as founders.
  • Founders were bred with C57BL/6JBomTac (Taconic), giving rise to litters containing B6;D2-Tg(STC2)N1 or B6;D2-Tg(STC2(C120A))N1 mice as well as wild-type littermates, which were genotyped and analyzed blinded for growth by consecutive weighing.
  • MEFs mouse embryonic fibroblasts
  • Transgenic STC2 contained in the media of confluent plates was immunoprecipitated from 20 ml of media using 30 ⁇ l of Protein G Sepharose 4 Fast Flow (GE Healthcare), to which mAb STC221 was immobilized at 2 mg ml ⁇ 1 by using dimethyl pimelimidate dihydrochloride (Sigma) cross-linking, essentially as described. Eluted protein was assessed for the presence of endogenous murine PAPP-A by Western blotting using mAb D8-mlgG2a.
  • STC1 and STC2 function in vitro as proteinase inhibitors of the pappalysin family of metalloproteinases, comprised of PAPP-A and PAPP-A2.
  • STC1 exerts its inhibitory function by forming a high-affinity proteinase-inhibitor complex, while STC2 inhibitory activity requires that it forms a covalent complex with its target proteinase.
  • the homologous STCs have unique amino acid sequences with no known modules or motifs by which this biochemical function might have been predicted.
  • mice transgenic for STC2 To test our prediction that overexpression of STC2 causes growth retardation by proteolytic inhibition, we generated and compared mice transgenic for STC2 and
  • STC2(C120A) STC2(C120A).
  • STC2 overexpression caused a severe reduction in postnatal growth rate compared to nontransgenic animals ( FIG. 14 a ).
  • Our data further indicate a correlation between the circulating level of STC2 and the severity of the growth retardation ( FIG. 14 b ).
  • transgenic expression of STC2(C120A) did not cause a detectable alteration in growth rate, even at high levels of circulating protein ( FIG. 14 c ).
  • Dysregulated IGF receptor signaling has been extensively linked to various diseases, in particular human cancer. Also, the involvement of PAPP-A in cancer development is increasingly recognized, and is underscored by the finding that PAPP-A knockout mice have a remarkably low incidence of spontaneous cancers of age. It is therefore interesting that multiple reports link STC1 or STC2 to human cancers. For example, loss of BRCA1 tumor suppressor function in breast cancer causes STC1 expression to become undetectable, and late relapse of breast cancer correlates with high expression of STC1 and STC2.
  • the mammalian stanniocalcins are novel proteinase inhibitors of the complex extracellular network that regulates IGF receptor activation in vivo.
  • Murine PAPP-A2 primer SEQ ID NO: 8 5′-GAGCTTCTCTTTTAGTCTGCCCCC
  • Murine PAPP-A2 primer SEQ ID NO: 9 5′-CCGGGGTACCATGATGTGTTGGAAGGTCCTGAG
  • Murine PAPP-A2 primer SEQ ID NO: 10 5′-GATGGTGAGCGGTATGTCACAA
  • Murine PAPP-A2 primer SEQ ID NO: 11 5′-CCGGTCCAGGCGGATACCCT
  • Murine PAPP-A2 primer SEQ ID NO: 12 5′-GATCTCTAGATTACTGGTTTTCTTCTGCCTTGGGG STC2 primer SEQ ID NO: 13 5′-GCACAGGTTCGGCGCCATAAGCCGGAAGTG STC2 primer SEQ ID NO: 14 5′-CACTTCCGGCTTATGGCGCCGAACCTGTGC STC2 primer SEQ ID NO: 15 5′-CAGCGTGCAGGTTCAGGCTGAGCAGAACTGGGGAAG STC2 primer SEQ ID NO

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Biochemistry (AREA)
  • Genetics & Genomics (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Zoology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biophysics (AREA)
  • Immunology (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Wood Science & Technology (AREA)
  • Biomedical Technology (AREA)
  • Endocrinology (AREA)
  • General Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Toxicology (AREA)
  • Dermatology (AREA)
  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Reproductive Health (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Vascular Medicine (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
US14/889,997 2013-05-10 2014-05-12 Pappalysin Regulator Abandoned US20160151405A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DKPA201370259 2013-05-10
DKPA201370259 2013-05-10
PCT/DK2014/050131 WO2014180485A2 (en) 2013-05-10 2014-05-12 Pappalysin regulator

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/DK2014/050131 A-371-Of-International WO2014180485A2 (en) 2013-05-10 2014-05-12 Pappalysin regulator

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US16/599,706 Continuation US11318158B2 (en) 2013-05-10 2019-10-11 Pappalysin regulator

Publications (1)

Publication Number Publication Date
US20160151405A1 true US20160151405A1 (en) 2016-06-02

Family

ID=50943008

Family Applications (2)

Application Number Title Priority Date Filing Date
US14/889,997 Abandoned US20160151405A1 (en) 2013-05-10 2014-05-12 Pappalysin Regulator
US16/599,706 Active US11318158B2 (en) 2013-05-10 2019-10-11 Pappalysin regulator

Family Applications After (1)

Application Number Title Priority Date Filing Date
US16/599,706 Active US11318158B2 (en) 2013-05-10 2019-10-11 Pappalysin regulator

Country Status (9)

Country Link
US (2) US20160151405A1 (https=)
EP (1) EP2994158A2 (https=)
JP (1) JP2016520583A (https=)
CN (1) CN105263510A (https=)
CA (1) CA2911933A1 (https=)
EA (1) EA201591894A1 (https=)
HK (1) HK1215929A1 (https=)
MX (1) MX2015015519A (https=)
WO (1) WO2014180485A2 (https=)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115835879A (zh) * 2020-06-30 2023-03-21 国立大学法人东北大学 Stat3磷酸化抑制剂、自身免疫性疾病和冠状病毒传染病的预防或治疗剂
TW202235618A (zh) * 2021-01-05 2022-09-16 美國馬友醫藥教育研究基金會 治療眼內壓相關疾患
WO2022270926A1 (ko) * 2021-06-22 2022-12-29 동아대학교 산학협력단 다양한 암의 진단, 전이 또는 예후 예측용 신규한 바이오마커 및 이의 용도
WO2024042220A1 (en) * 2022-08-25 2024-02-29 Aarhus Universitet Modulators of papp-a activity
TW202432584A (zh) 2022-11-15 2024-08-16 美商嘉來克生命科學有限責任公司 抗papp-a抗體及其使用方法
WO2026008015A1 (en) * 2024-07-05 2026-01-08 The University Of Hong Kong Stanniocalcin 2 (stc2) and derivatives as anti-diabetic agents

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5994103A (en) * 1995-06-02 1999-11-30 Human Genome Science, Inc. Human stanniocalcin-alpha
CA2387685A1 (en) * 1999-10-27 2001-05-03 Human Genome Sciences, Inc. Stanniocalcin proteins and nucleic acids and methods based thereon
CA2389751A1 (en) 1999-11-01 2001-05-10 Curagen Corporation Differentially expressed genes involved in angiogenesis, the polypeptides encoded thereby, and methods of using the same
WO2005035732A2 (en) 2003-02-19 2005-04-21 Dyax Corporation Papp-a ligands
WO2008101118A2 (en) 2007-02-14 2008-08-21 The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services A gene expression signature identifying pro-angiogenic genes in ovarian tumor endothelial cell isolates
US20100292303A1 (en) 2007-07-20 2010-11-18 Birrer Michael J Gene expression profile for predicting ovarian cancer patient survival
AU2009207645B2 (en) 2008-01-25 2014-11-13 Aarhus Universitet Selective exosite inhibition of PAPP-A activity against IGFBP-4
WO2010020004A1 (en) * 2008-08-22 2010-02-25 Children's Medical Research Institute Compositions and methods for inhibition of adipogenesis and the treatment of obesity

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
Bowie et al, 1990, Science 247:1306-1310, especially p.1306, column 2, paragraph 2 *
Ngo et al., 1994, The Protein Folding Problem and Tertiary Structure Prediction, Merz et al., eds, Birkhauser, Boston, pp. 433-506 *
Wang et al 2001. J. Biol Chem. 276:49213-49220 *
Wells, 1990, Biochemistry 29:8509-8517 *

Also Published As

Publication number Publication date
HK1215929A1 (zh) 2016-09-30
WO2014180485A3 (en) 2015-03-05
US20200261490A1 (en) 2020-08-20
JP2016520583A (ja) 2016-07-14
EP2994158A2 (en) 2016-03-16
WO2014180485A2 (en) 2014-11-13
MX2015015519A (es) 2016-07-21
US11318158B2 (en) 2022-05-03
CN105263510A (zh) 2016-01-20
CA2911933A1 (en) 2014-11-13
EA201591894A1 (ru) 2016-04-29

Similar Documents

Publication Publication Date Title
US11318158B2 (en) Pappalysin regulator
US10941200B2 (en) TREM2 cleavage modulators and uses thereof
EP2172220B1 (en) Methods of diagnosing and treating pre-eclampsia or eclampsia
WO2017147742A1 (en) Gfral receptor therapies
CN101506239B (zh) 抗人α9整联蛋白抗体及其用途
EA025218B1 (ru) Способ диагностики злокачественных новообразований, экспрессирующих рецептор her2 или его укороченные варианты
Schenk et al. Tenascin‐C in serum: a questionable tumor marker
KR101560843B1 (ko) 페리오스틴의 Ｅｘｏｎ-17 부위에 의해 코드되는 펩티드에 대한 항체를 함유하는 암 치료제
JP2025176044A (ja) 抗ｎａｍｐｔ抗体及びその用途
RU2770006C2 (ru) Антитела к фактору ix padua
EP1978034B1 (en) Anti-periostin antibody and pharmaceutical composition containing the same for preventing or treating periostin-related disease
KR20120064072A (ko) 콜라겐 네오에피토프 항체
CN101103044B (zh) 抗α9整联蛋白抗体及其用途
JP2010512781A (ja) Ｖｅｇｆｒの変化体ならびに妊娠関連の医学的状態の診断および処置におけるその使用
WO2013001819A1 (ja) 可溶性インテグリンα４変異体
Hamaoka et al. Anti-human HB-EGF monoclonal antibodies inhibiting ectodomain shedding of HB-EGF and diphtheria toxin binding
US20120122107A1 (en) Homeostatic multidomain protein, and uses for it
JP7316592B2 (ja) 抗ｎｉｎｊ－１抗体及びその使用
GB2546773A (en) Cancer
TW201840588A (zh) 抗ｇｐｒ２０抗體
JPWO2005056597A1 (ja) 免疫グロブリンＦｃ受容体タンパク質
WO2015150815A1 (en) Methods and materials relating to auto-immune disease
JP2024542100A (ja) Ｘｘｉｉ型コラーゲンアッセイ
HK40080584A (en) Anti-nampt antibodies and uses thereof
JP2009031307A (ja) 絨毛外栄養膜細胞特異的蛋白質

Legal Events

Date Code Title Description
AS Assignment

Owner name: AARHUS UNIVERSITET, DENMARK

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:OXVIG, CLAUS;MIKKELSEN, JAKOB HAUGE;JEPSEN, MALENE RUNGE;SIGNING DATES FROM 20151218 TO 20151221;REEL/FRAME:037651/0775

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION