Classifications

• • 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
  • C07K14/52—Cytokines; Lymphokines; Interferons
  • C07K14/54—Interleukins [IL]
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • 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
  • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
  • C07K14/715—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons
  • C07K14/7155—Receptors; Cell surface antigens; Cell surface determinants for cytokines; for lymphokines; for interferons for interleukins [IL]

Definitions

• the present invention relates to gastric cancer, and more particularly to a new treatment for combating this cancer.
• Stomach cancer is the second most common cancer in the world, accounting for about 10% of all cancer cases.
• the people most likely to contract this pathology have for the most part a diet rich in starch, low in fat, proteins, fruits and fresh vegetables. Salt, alcohol and excessive consumption of smoked foods are also involved.
• An infection caused by Helicobacter pylori is also often implicated.
• stomach cancer causes only a few symptoms, which are often uncharacteristic, making early diagnosis even more difficult.
• the most common symptom is pain in the upper and middle part of the belly.
• the patient is prone to weight loss, vomiting, anemia, the presence of blood in the stool.
• the diagnosis is usually made by endoscopy or fibroscopy, which can detect small cancerous tumors at an early stage, tumors sometimes benign or other lesions present on the gastric mucosa.
• Curative treatment is usually partial or complete gastrectomy.
• chronic atrophy gastritis the eradication of H. pylori is also important.
• There is currently no consensus chemotherapy protocol. Improvement in survival and quality of life compared to simple symptomatic treatment is moderate. It is therefore important from a clinical point of view to propose new treatment alternatives to the clinician.
• the present invention proposes to solve the disadvantages of the state of the art by presenting new biological tools to improve the diagnosis and treatment of a patient against gastric cancer.
• the inventors have shown that interleukin 17 F (IL 17 F), just like interleukin 17 A (IL 17 A), plays a very important role in gastric cancer.
• the invention relates to the use of at least one interleukin 17 inhibitor and / or at least one TIL17 receptor inhibitor, for the preparation of a medicament intended for inhibition, the prevention or treatment of gastric cancer.
• the interleukin 17 is interleukin 17 A (TL 17A) or interleukin 17F (IL 17F).
• said TIL17 receptor is TIL17 receptor A or TIL17 receptor C.
• the interleukin-17 inhibitor is an antibody directed against IL17, preferentially against IL17A or F and / or the inhibitor of said IL-17 receptor is an antibody directed against the IL-17 receptor. , preferably against the receptor A or C of IL 17.
• the interleukin 17 inhibitor is an interfering RNA with IL 17, preferentially against
• TIL17A or F and / or the inhibitor of said TIL17 receptor is an RNA interfering with the IL 17 receptor, preferentially against the TIL17 receptor A or C.
• the invention also relates to a pharmaceutical composition comprising as active substance at least one interleukin 17 inhibitor and / or at least one inhibitor of a TIL17 receptor in combination with a pharmaceutically appropriate vehicle.
• the interleukin 17 is interleukin 17 A (TL 17A) or interleukin 17F (IL 17F).
• said TIL17 receptor is TIL17 receptor A or TIL17 receptor C.
• the interleukin-17 inhibitor is an antibody directed against IL17, preferentially against IL-17A or F and / or the inhibitor of said IL-17 receptor is an antibody directed against the IL-17 receptor.
• the interleukin 17 inhibitor is an interfering RNA with IL 17, preferably against TIL17A or F and / or the inhibitor of said TIL17 receptor is an RNA that interferes with the TIL17, preferably against the A or C receptor of the IL 17.
• the invention also relates to the use of the pharmaceutical composition as defined above for the inhibition, prevention and / or treatment of a gastric cancer.
• IL17 receptor is understood to mean a molecule of the IL-17 receptor family, the latter being defined by their cognate with the IL-17RA receptor (Moseley et al., 2003, Cytokine Growth Factor Rev, 14 (2 ): 155-74)
• said IL 17 receptor is the IL 17 receptor A or the TIL17 C receptor.
• IL-17RA receptor means the molecule initially discovered for its involvement in the inflammatory and / or immunostimulating activity of TIL-17A (Yao
• IL-17RC receptor is meant a molecule related to the IL-17RA receptor
• inhibitor of interleukin 17F is meant a molecule (or set of molecules) which blocks the inflammatory and / or immunostimulating activity of IL17F.
• the inhibitor may be in particular an antibody directed against IL17F, or an RNA that interferes with IL17.
• inhibitor of an IL17 receptor is meant a molecule (or set of molecules) that blocks the action of a TIL17 receptor.
• the inhibitor may be in particular an antibody, directed against the TIL17 receptor, preferentially against the TIL17 receptor A or C.
• the inhibitor may also be an RNA that interferes with the IL17 receptor, preferentially against the IL 17 receptor A or C.
• Gastric cancer means any cancer of the stomach.
• antibody is meant both an entire antibody and an antibody fragment.
• the recombinant antibodies can be obtained according to conventional methods known to those skilled in the art, from prokaryotic organisms, such as bacteria, or from eukaryotic organisms, such as yeasts, mammalian cells, plants, insects or animals, or by systems extracellular production.
• the monoclonal antibodies can be prepared according to conventional techniques known to those skilled in the art, such as the hybridoma technique, the general principle of which is recalled below.
• an animal usually a mouse (or cells cultured in the context of in vitro immunizations) is immunized with a target antigen of interest, whose B lymphocytes are then capable of producing antibodies against the said antigen. antigen.
• B lymphocytes are then capable of producing antibodies against the said antigen. antigen.
• These antibody-producing lymphocytes are then fused with "immortal" myeloma cells (murine in the example) to give rise to hybridomas. From the heterogeneous mixture of cells thus obtained, the cells capable of producing a particular antibody and of multiplying indefinitely are then selected.
• Each hybridoma is multiplied in the clone form, each leading to the production of a monoclonal antibody whose recognition properties with respect to the antigen of interest can be tested, for example by ELISA, by immunoblotting in one or two-dimensional, in immunofluorescence, or with a biosensor.
• the monoclonal antibodies thus selected are subsequently purified, in particular according to the affinity chromatography technique.
• antibody fragments can be obtained by proteolysis.
• they can be obtained by enzymatic digestion, resulting in Fab-type fragments (papain treatment, Porter RR, 1959, Biochem J., 73: 119-126) or F (ab) '2 type (treatment pepsin, Nisonoff A. et al., 1960, Science, 132: 1770-1771).
• Fab-type fragments papain treatment, Porter RR, 1959, Biochem J., 73: 119-126
• F (ab) '2 type treatment pepsin, Nisonoff A. et al., 1960, Science, 132: 1770-1771.
• they can also be prepared recombinantly (Skerra A., 1993,
• Another antibody fragment which is suitable for the purposes of the invention comprises a fragment Fv which is a dimer consisting of the non-covalent association of the light variable domain (VL) and the heavy variable domain (VH) of the Fab fragment, therefore of the association of two polypeptide chains.
• this fragment Fv can be modified by genetic engineering by inserting a peptide link adapted between the VL domain and the VH domain (Huston P. et al., 1988, Proc Natl.Acad.Sci.USA, 85: 5879-5883).
• fragment scFv single chain Fragment variable
• the use of a peptide bond preferably composed of 15 to 25 amino acids makes it possible to connect the C-terminal end of one domain to the N-terminus of the other domain, thus constituting a monomeric molecule with properties similar to those of the antibody in its complete form.
• the two orientations of the VL and VH domains are suitable (VL-link-VH and VH-link-VL) because they have identical functional properties.
• any fragment known to those skilled in the art and having the immunological characteristics defined above is suitable for the purposes of the invention.
• the antibody is directed against TIL17A or F or against the IL17 receptor, preferentially against the TIL17 or A receptor.
• interfering RNA is meant a ribonucleic acid which blocks the expression of a predetermined gene (Dallas A. et al., 2006, Med Sci Monit, 12 (4): RA67-74).
• the RNAi interferes with IL17, preferentially TIL17A or F or with the TIL17 receptor, preferentially the A or C receptor of TIL17.
• drug or pharmaceutical composition is meant any substance or composition presented as possessing curative or preventive properties with regard to human or animal diseases, as well as any product that can be administered to humans or animals in order to establish a medical diagnosis or restore, correct or modify their organic functions.
• active substance is meant a component recognized as having therapeutic properties.
• the active substances may be administered in unit dosage forms or in admixture with conventional pharmaceutical carriers, and intended for oral administration, for example in the form of a tablet, a capsule, an oral solution, etc., or rectally, in the form of a suppository, parenterally, in particular in the form of an injectable solution, especially intravenously, intradermally, subcutaneously, etc., according to conventional protocols well known to those skilled in the art.
• the active substances can be used in creams, ointments, lotions.
• the active substances are mixed with a pharmaceutically acceptable excipient also called a pharmaceutically suitable vehicle, such as gelatin, starch, lactose, magnesium stearate, talc, gum Arabic or the like.
• a pharmaceutically suitable vehicle such as gelatin, starch, lactose, magnesium stearate, talc, gum Arabic or the like.
• the tablets may be coated with sucrose, a cellulose derivative, or other suitable materials. They can also be treated in such a way that they have prolonged or delayed activity and that they continuously release a predetermined quantity of active substances.
• a preparation in capsules can also be obtained by mixing the active substances with a diluent and pouring the mixture into soft or hard gelatin capsules.
• a preparation in the form of a syrup or for administration in the form of drops in which the active substances are present together with a sweetening agent, an antiseptic, such as, in particular, methylparaben and propylparaben, and a reducing agent. taste or a suitable color.
• the water-dispersible powders or granules may contain the active substances in admixture with dispersants or wetting agents, or suspending agents, well known to those skilled in the art.
• aqueous suspensions for parenteral administration, use is made of aqueous suspensions, isotonic saline solutions or sterile and injectable solutions which contain dispersing agents, pharmacologically compatible wetting agents, such as in particular propylene glycol or butylene glycol.
• the drug or pharmaceutical composition according to the invention may further comprise an activating agent which induces the effects of a medication or enhances or supplements the effects of the main medication, in particular by increasing the bioavailability of the main medication.
• the dosage depends on the severity of the condition.
• the administration may in particular be administered once every 2 to 8 weeks, preferably from 50 to 100 mg of of antibodies, in combination with a pharmaceutically acceptable excipient.
• a pharmaceutical composition comprising interfering RNA the administration may in particular be administered once every 2 to 8 weeks, preferably from 1 to 10 mg / kg of interfering RNA, in combination with a pharmaceutically acceptable excipient. .
• the invention also relates to an in vitro method for determining, from a biological sample, the early diagnosis of a gastric cancer characterized in that the expression of the gene encoding TIL-17A, TIL-17F, TIL is determined. -17RA and / or IL-17RC.
• Measurement of the expression of the gene encoding TIL-17A, TIL-17F, TIL-17RA and / or IL-17RC comprises the following steps: a. biological material is extracted from the biological sample, b. the biological material is brought into contact with at least one reagent specific for the gene encoding IL17-A, IL17-F, IL17-RA and / or IL17RC; vs. the expression of the gene encoding TIL17-A, TIL17-F, TIL17-RA and / or IL17RC is determined.
• the biological material extracted in step a) may comprise nucleic acids or proteins.
• Said specific reagent of step b) may comprise a hybridization probe or an antibody specific for the gene encoding IL-17A, IL-17F, IL-17RA and / or IL-17RC.
• the invention also relates to the use of at least one specific reagent of the gene encoding IL-17A, IL-17F, IL-17RA and / or IL-17RC to determine the early diagnosis of a gastric cancer.
• the invention also relates to a kit for early diagnosis of gastric cancer comprising at least one reagent specific for the gene encoding TIL-17A, TIL-17F, IL-17
• TIL-17A, IL-17F, IL-17RA and / or IL-17RC provides a tool for the diagnosis of gastric cancer.
• the expression of the target gene can be analyzed in a patient susceptible to to develop gastric cancer, and compare with known mean expression values of the target gene of gastric cancer patients and known mean expression values of the target gene of healthy patients.
• biological sample is intended to mean any sample taken from a patient, and capable of containing a biological material as defined below.
• This biological sample can be in particular a sample of blood, serum, tissue, patient.
• This biological sample is available by any type of sampling known to those skilled in the art.
• the biological sample taken from the patient is a blood sample.
• the biological material is extracted from the biological sample by all the protocols for extraction and purification of nucleic acids or proteins known to those skilled in the art.
• the term "biological material” means any material making it possible to detect the expression of a target gene.
• the biological material may comprise, in particular, proteins, or nucleic acids such as in particular deoxyribonucleic acids (DNA) or ribonucleic acids (RNA).
• the nucleic acid may in particular be an RNA (ribonucleic acid).
• the biological material extracted during step a) comprises nucleic acids, preferably RNAs, and even more preferably total RNAs.
• Total RNAs include transfer RNAs, messenger RNAs (mRNAs), such as mRNAs transcribed from the target gene, but also transcribed from any other gene and ribosomal RNAs.
• This biological material comprises material specific for a target gene, such as, in particular, the transcribed mRNAs of the target gene or the proteins derived from these mRNAs, but may also comprise non-specific material of a target gene, such as in particular the mRNAs transcribed from the target gene.
• a gene other than the target gene tRNAs, rRNAs from genes other than the target gene.
• the extraction of nucleic acids can be carried out by: a step of lysis of the cells present in the biological sample, in order to release the nucleic acids contained in the cells of the patient.
• a step of lysis of the cells present in the biological sample in order to release the nucleic acids contained in the cells of the patient.
• lysis methods as described in patent applications WO 00/05338, WO 99/53304 and WO 99/15321.
• Those skilled in the art may use other well-known lysis methods, such as thermal or osmotic shocks or chemical lyses with chaotropic agents such as guanidium salts (US Pat. No. 5,234,809).
• a purification step allowing separation between the nucleic acids and the other cellular constituents released in the lysis step.
• This step generally allows the nucleic acids to be concentrated, and may be suitable for the purification of DNA or RNA.
• magnetic particles optionally coated with oligonucleotides by adsorption or covalence (see in this regard US Pat. No. 4,672,040 and US Pat. No. 5,750,338), and thus to purify the nucleic acids that have attached to these magnetic particles. , by a washing step.
• This nucleic acid purification step is particularly advantageous if it is desired to subsequently amplify said nucleic acids.
• the first step generally consists, as for nucleic acids in lysing cells.
• An osmotic shock may be sufficient to break the cell membrane of fragile cells, which may be performed in the presence of a detergent.
• Mechanical action can also be added to the process (piston homogenizer for example). Lysis can also be induced by ultrasound, by mechanical lysis using glass beads.
• Extraction of proteins of interest can then be carried out by chromatography, such as in particular on a gel chromatography column, filled with a resin consisting of hollow and porous beads. The pore size of these beads is such that the proteins are separated according to their size.
• ion exchange column chromatography which allows the extraction of proteins according to their electrostatic affinity to groups charged with the resin.
• the term "specific reagent” means a reagent which, when it is brought into contact with biological material as defined above, binds with the specific material of said gene. target.
• a reagent which, when it is brought into contact with biological material as defined above, binds with the specific material of said gene. target.
• the specific reagent and the biological material are of nucleic origin, contacting the specific reagent and the biological material allows hybridization of the specific reagent with the specific material of the target gene.
• hybridization is meant the process in which, under appropriate conditions, two nucleotide fragments bind with stable and specific hydrogen bonds to form a double-stranded complex.
• hybridization can be partial (we then speak of nucleotide fragments or sufficiently complementary sequences), that is to say that the double-stranded complex obtained comprises A-T bonds and CG bonds making it possible to form the double-stranded complex, but also bases not linked to a complementary base.
• Hybridization between two nucleotide fragments depends on the operating conditions that are used, and in particular on stringency. The stringency is defined in particular according to the base composition of the two nucleotide fragments, as well as by the degree of mismatch between two nucleotide fragments.
• the stringency may also be a function of the reaction parameters, such as the concentration and type of ionic species present in the the hybridization solution, the nature and the concentration of denaturing agents and / or the hybridization temperature. All these data are well known and the appropriate conditions can be determined by those skilled in the art.
• the hybridization temperature is between approximately 20 and 70 ° C., in particular between 35 and 65 ° C., in a saline solution at a concentration of approximately 0 ° C. , 5 to 1 M.
• a sequence, or nucleotide fragment, or oligonucleotide, or polynucleotide is a sequence of nucleotide units joined together by phosphoric ester bonds, characterized by the informational sequence of natural nucleic acids, which can hybridize to a nucleotide fragment, the sequence may contain monomers of different structures and be obtained from a natural nucleic acid molecule and / or by genetic recombination and / or chemical synthesis.
• a unit is derived from a monomer which may be a natural nucleotide nucleic acid whose constituent elements are a sugar, a phosphate group and a nitrogen base; in the DNA sugar is deoxy-2-ribose, in RNA the sugar is ribose; depending on whether it is DNA or RNA, the nitrogenous base is chosen from adenine, guanine, uracil, cytosine, thymine; or the monomer is a modified nucleotide in at least one of the three constituent elements; for example, the modification can take place either at the level of the bases, with modified bases such as inosine, methyl-5-deoxycytidine, deoxyuridine, dimethylamino-5-deoxyuridine, diamino-2,6-purine, bromo Deoxyuridine or any other modified base capable of hybridization, either at the sugar level, for example the replacement of at least one deoxyribose with a polyamide, or at the level of the phosphate
• the specific reagent comprises at least one amplification primer.
• amplification primer is intended to mean a nucleotide fragment comprising from 5 to 100 nucleic motifs, preferably from 15 to 30 nucleic motifs, allowing the initiation of an enzymatic polymerization, such as in particular a reaction.
• enzymatic amplification By enzymatic amplification reaction is meant a process generating multiple copies of a nucleotide fragment by the action of at least one enzyme.
• PCR Polymerase Chain Reaction
• the specific reagent comprises at least 2 amplification primers, specific for the target gene, in order to allow the amplification of the specific material of the target gene.
• the specific material of the target gene then preferably comprises a complementary DNA obtained by reverse transcription of messenger RNA from the target gene (this is called target gene specific cDNA) or a complementary RNA obtained by transcription of gene-specific cDNAs. target (this is called specific cRNA of the target gene).
• target gene specific cDNA a complementary DNA obtained by reverse transcription of messenger RNA from the target gene
• target this is called specific cRNA of the target gene.
• the specific reagent of step b) comprises at least one hybridization probe.
• Hybridization probe is understood to mean a nucleotide fragment comprising at least 5 nucleotide motifs, such as from 5 to 100 nucleic motifs, in particular from 10 to 35 nucleic motifs, having hybridization specificity under determined conditions to form a complex of nucleotides. hybridization with the specific material of a target gene.
• the specific material of the target gene may be a nucleotide sequence comprised in a messenger RNA derived from the target gene (referred to as mRNA specific for the target gene), a nucleotide sequence included in a complementary DNA obtained by reverse transcription.
• the hybridization probe may comprise a marker for its detection. Detection means either direct detection by a physical method or indirect detection by a detection method using a marker. Many detection methods exist for the detection of nucleic acids. [See, for example, Kricka et al, Clinical Chemistry, 1999, No. 45 (4), p.453-458 or Keller GH et al, DNA Probes, 2nd Ed., Stockton Press, 1993, sections 5 and 6, p. 173-249].
• marker is meant a tracer capable of generating a signal that can be detected.
• tracers includes enzymes that produce a detectable signal for example by colorimetry, fluorescence or luminescence, such as horseradish peroxidase, alkaline phosphatase, beta-galactosidase, glucose-6-phosphate dehydrogenase; chromophores such as fluorescent, luminescent or coloring compounds; electron density groups detectable by electron microscopy or by their electrical properties such as conductivity, by amperometry or voltammetry methods, or by impedance measurements; groups detectable by optical methods such as diffraction, surface plasmon resonance, contact angle variation or by physical methods such as atomic force spectroscopy, tunneling effect, etc. ; radioactive molecules such as 32P, 35S or 1251.
• the hybridization probe may be a so-called detection probe.
• the so-called detection probe is labeled by means of a marker as defined above.
• the detection probe may in particular be a "molecular beacon” detection probe as described by Tyagi & Kramer (Nature biotech, 1996, 14: 303-308). These "molecular beacons” become fluorescent during hybridization. They have a stem-loop structure and contain a fluorophore and a "quencher” group. Attachment of the specific loop sequence with its target nucleic acid complement sequence causes stem unwinding and fluorescent signal emission upon excitation at the appropriate wavelength.
• labeled target sequences can be used directly (in particular by the incorporation of a marker within the target sequence) or indirectly (especially by the use of a detection probe as defined above) the target sequence.
• it is possible to carry out a step of labeling and / or cleavage of the target sequence before the hybridization step for example by using a labeled deoxyribonucleotide triphosphate during the enzymatic amplification reaction. Cleavage can be achieved in particular by the action of imidazole and manganese chloride.
• the target sequence may also be labeled after the amplification step, for example by hybridizing a detection probe according to the sandwich hybridization technique described in WO 91/19812. Another particular preferred mode of nucleic acid labeling is described in application FR 2 780 059.
• the detection probe comprises a flurophore and a quencher.
• the hybridization probe may also be a so-called capture probe.
• the so-called capture probe is immobilized or immobilizable on a solid support by any appropriate means, that is to say directly or indirectly, for example by covalence or adsorption.
• a solid support it is possible to use synthetic materials or natural materials, optionally chemically modified, in particular polysaccharides such as cellulose-based materials, for example paper, cellulose derivatives such as cellulose acetate and cellulose.
• nitrocellulose or dextran polymers, copolymers, especially based on styrene-type monomers, natural fibers such as cotton, and synthetic fibers such as nylon; mineral materials such as silica, quartz, glasses, ceramics; latexes; magnetic particles; metal derivatives, gels etc.
• the solid support may be in the form of a plate of microtitration of a membrane as described in WO-A-94/12670, of a particle.
• step c) the determination of the expression of the target gene can be carried out by all the protocols known to those skilled in the art.
• the expression of a target gene can be analyzed by the detection of the mRNAs (messenger RNAs) which are transcribed from the target gene at a given instant or by the detection of the proteins derived from these mRNAs.
• mRNAs messenger RNAs
• the invention preferably relates to determining the expression of a target gene by detecting mRNAs derived from this target gene.
• step c) of the method according to the invention determines the expression of a target gene as follows:
• RNAs including the transfer RNAs (tRNAs), the ribosomal RNAs (rRNAs) and the messenger RNAs (mRNA)
• tRNAs transfer RNAs
• rRNAs ribosomal RNAs
• mRNA messenger RNAs
• this reverse transcription reaction can be carried out using a reverse transcriptase enzyme which makes it possible to obtain, from an RNA fragment, a complementary DNA fragment.
• AMV Avian Myoblastosis Virus
• MMLV Moloney Murine Leukemia Virus
• this reverse transcription step is carried out in the presence of nucleotide fragments comprising only thymine (polyT) bases, which hybridize by complementarity on the polyA sequence of the mRNAs to form a polyT-polyA complex which then serves as a starting point for the reverse transcription reaction carried out by the reverse transcriptase enzyme.
• Complementary cDNAs are thus obtained from the mRNAs resulting from a target gene (cDNA specific for the target gene) and cDNAs complementary to mRNAs originating from genes other than the target gene (non-specific cDNA of the target gene).
• the specific amplification primer or primers of a target gene are brought into contact with the cDNAs specific for the target gene and the nonspecific cDNAs of the target gene.
• the target gene specific amplification primer (s) hybridize with the target gene specific cDNAs and specifically amplify a predetermined region of known length of the cDNAs from the mRNAs from the target gene.
• the non-specific cDNAs of the target gene are not amplified, whereas a large quantity of cDNA specific to the target gene is then obtained.
• it is indifferently referred to as "target gene-specific cDNAs" or "cDNAs from mRNAs derived from the target gene”. This step may be carried out in particular by a PCR type amplification reaction or by any other amplification technique as defined above.
• step 2) determining the expression of the target gene by detecting and quantifying the target gene-specific cDNAs obtained in step 2) above.
• This detection can be performed after electrophoretic migration of the cDNAs specific for the target gene according to their size.
• the gel and the migration medium may comprise ethydium bromide to enable the direct detection of the target gene specific cDNAs when the gel is placed, after a given migration time, on a UV light table (ultra violet) by the emission of a light signal. This signal is all the brighter as the amount of cDNA specific to the target gene is important.
• Specific cDNAs of the target gene can also be detected and quantified by the use of a quantization range obtained by an amplification reaction conducted to saturation.
• the expression of a target gene of different groups of patients by the simultaneous determination of the expression of a so-called household gene, the expression of which is similar in the different groups of patients.
• By realizing a relationship between the expression of the target gene and the expression of the household gene ie by realizing a ratio between the amount of cDNA specific for the target gene, and the amount of cDNA specific for the gene of household, thus correcting any variability between different experiments.
• Those skilled in the art may refer in particular to the following publications: Bustin SA, J Mol Endocrinol, 2002, 29: 23-39; Giulietti A Methods, 2001, 25: 386-401.
• the expression of a target gene can be determined as follows:
• a reverse transcription step is carried out, as described above, for cDNAs complementary to the mRNAs resulting from a target gene (specific cDNA) target gene) and complementary cDNAs of mRNAs from genes other than the target gene (non-specific cDNA of the target gene).
• the hybridization reaction can be carried out on a solid support which includes all the materials as indicated above.
• the hybridization probe is immobilized on a support.
• the hybridization reaction may be preceded by a step of enzymatic amplification of the target gene specific cDNAs as described above to obtain a large amount of cDNA specific to the target gene and increase the probability that a specific cDNA of a The target gene hybridizes to a capture probe specific for the target gene.
• the hybridization reaction may also be preceded by a step of labeling and / or cleaving the cDNAs specific for the target gene as described above, for example using a labeled deoxyribonucleotide triphosphate for the amplification reaction. Cleavage can be achieved in particular by the action of imidazole and manganese chloride.
• the specific cDNA of the target gene may also be labeled after the amplification step, for example by hybridizing a labeled probe according to the sandwich hybridization technique described in document WO-A-91/19812. Other particular preferred modes of labeling and / or nucleic acid cleavage are described in the applications WO 99/65926, WO 01/44507, WO 01/44506, WO 02/090584, WO 02/090319. 3) a step of detecting the hybridization reaction is then carried out. The detection can be carried out by contacting the support on which the target gene-specific capture probes are hybridized with the target gene-specific cDNAs with a detection probe, labeled with a marker, and the signal emitted by the target gene is detected. the marker. When the specific cDNA of the target gene has been previously labeled with a marker, the signal emitted by the marker is detected directly.
• the expression of a target gene can also be determined as follows:
• a reverse transcription step is carried out in order to obtain the cDNAs of the mRNAs of the biological material.
• the polymerization of the complementary RNA of the cDNA is then carried out by the use of a T7 polymerase enzyme which functions under the control of a promoter and which makes it possible to obtain, from a DNA template , complementary RNA.
• the cRNAs of the cDNAs of the mRNAs specific for the target gene are then obtained (this is called target gene specific cRNA) and the cRNAs of the cDNAs of the nonspecific mRNAs of the target gene.
• the cRNAs are brought into contact with a support, on which are immobilized capture probes specific for the target gene whose expression is to be analyzed, in order to carry out a hybridization reaction between the target gene specific cRNAs and the capture probes, the nonspecific cRNAs of the target gene do not not hybridizing on capture probes.
• the hybridization reaction may also be preceded by a step of labeling and / or cleaving the target gene specific cRNAs as described above.
• a step of detecting the hybridization reaction is then carried out.
• the detection can be carried out by contacting the support on which the target gene-specific capture probes are hybridized with target gene-specific cNNAc with a detection probe, labeled with a marker, and the signal emitted by the target is detected. marker pen.
• the cRNA specific for the target gene has been previously labeled with a marker, the signal emitted by the marker is detected directly.
• the use of cRNA is particularly advantageous when using a biochip type support on which is hybridized a large number of probes.
• steps B and C are performed at the same time.
• This preferred mode can be implemented in particular by "NASBA in real time” which combines in a single step the NASBA amplification technique and real-time detection that uses “molecular beacons”.
• the NASBA reaction occurs in the tube, producing single-stranded RNA with which specific "molecular beacons” can hybridize simultaneously to give a fluorescent signal.
• the formation of the new RNA molecules is measured in real time by continuous control of the signal in a fluorescent reader.
• step c) can be carried out in particular by Western Blot or ELISA, or any other method known to those skilled in the art.
• the ELISA technique is a reference biochemical technique used in immunology to detect the presence of an antibody or an antigen in a sample.
• the technique uses two antibodies, one of which is specific for the antigen and the other is coupled to an enzyme.
• the Western Blot technique is a test for detecting a specific protein in a sample using an antibody specific for this protein comprising the following steps:
• the first step is gel electrophoresis, which separates the proteins from the sample according to their size.
• the proteins in the gel are then transferred to a membrane (nitrocellulose, PVDF, etc.) by pressure or by application of an electric current, the proteins being attached to the membrane by means of hydrophobic and ionic interactions.
• a first antibody specific for the protein to be studied (primary antibody) is incubated with the membrane.
• the membrane is then rinsed to remove unbound primary antibodies and incubated with so-called secondary antibodies, which will bind to the primary antibodies.
• This secondary antibody is usually linked to an enzyme that allows the visual identification of the protein studied on the membrane.
• the addition of a substrate of the enzyme generates a colored reaction that is visible on the membrane.
• Figure 1 shows the effects of IL-17A and IL-17F on IL-8 secretion of AGS cells.
• AGS cells were cultured in the presence or absence of
• FIG. 2 shows the effects of TIL17A and TIL17F on MAPK (mitogen-activated protein kinase) activation of AGS cells.
• MAPK mitogen-activated protein kinase
• FIG. 3 shows the effects of TIL17A and TIL17F on AP-I activation of AGS cells.
• AGS cells were cultured in serum
• Figure 5 shows the inhibition of the gene encoding TIL-17R (A) and IL 17RC (B) by interfering RNA (RNAi).
• AGS cells IxIO 5
• IxIO 5 interfering RNA
• Expression in IL-17R and IL-17RC mRNA normalized with GAPDH was analyzed 36 h after transfection by quantitative RT-PCR. The results are presented by the mean ⁇ SEM obtained on duplicates. * P ⁇ 0.05, compared to cells transfected with RNAi control.
• Figure 6 shows the effects of the inhibition of genes encoding IL-17R and IL-17RC on DNA binding activity of p65 NFKB (A) and c-jun AP-I (B).
• AGS cells IxIO 5
• IL-17R RNAi RNAi IL-17RC
• siRNA control 24 hours after transfection, the cells were placed in serum medium for 24h, then treated with 50 ng / ml IL-17A or IL-17F.
• the DNA binding activity of p-65 (A) was analyzed by a TransAM TM NFKB kit.
• MRNA expression of c-Jun (B) was analyzed by quantitative RT-PCR 30 min after stimulation. The results are presented by the mean ⁇ SEM obtained on duplicates. * P ⁇ 0.05, compared to cells transfected with RNAi control.
• a human gastric cancer cell line from the ATCC collection was used and cultured (37 ° C, 5% CO 2 ) in DMEM medium (Dulbecco's Modified Eagle's Medium, Invitrogen Life Technologies, Carlsbad, CA) supplemented with fetal calf serum (10% v / v).
• DMEM medium Dulbecco's Modified Eagle's Medium, Invitrogen Life Technologies, Carlsbad, CA
• fetal calf serum 10% v / v
• IL-8 ELISA AGS cells were stimulated with recombinant human IL17A or IL 17F (rhIL17A, rhIL17F, R & D Systems, USA) at a concentration of 50 ng / ml for 12h or 24h.
• the amount of IL8 secreted by the cultured cell was determined by ELISA (Diaclone, France). Western Blotting.
• the AGS cells were cultured in serum-depleted DMEM for 24 h, then treated with IL-17A or IL-17F at a concentration of 50 ng / ml or 200 ng / ml for 30 minutes. Activation of MAPKs was analyzed in Western blotting in the presence or absence of IL-17A and IL-17F.
• the cells were lysed in a lysis medium (20mM Hepes pH 7.7, 2.5mM MgCl 2 , 0.ImM EDTA, 20mM ⁇ -Glycerophosphate, 10OmM NaCl, 0.05% Triton X100, 0.5mM DTT, 0.ImM Na3VO4 , 20 ⁇ g / ml leupeptin, 20 ⁇ g / ml aprotinin, 100 ⁇ g / ml PMSF), and the protein concentration was determined by a BCA kit (Pierce, USA). Aliquots containing 80 ⁇ g of protein were used in gel electrophoresis comprising 10% SDS-polyacrylamide.
• the proteins were transferred from the gel to a nitrocellulose membrane (Amersham, USA).
• the membranes were then saturated (5% milk powder, 0.01% Tween20, 2% fetal calf serum) for 1 hour, then washed 3 times in PBS medium containing 0.1% Tween 20.
• the membranes were then placed in contact with each other.
• Activation of transcription factors were cultured in serum-depleted DMEM for 24 h, then treated with TIL-17A or IL-17F at a concentration of 50 ng / ml for 1 h.
• Nuclear protein extracts were obtained from cell lines by a kit (Active Motif, USA).
• the DNA binding activity of the C-jun factors, c-fos or p65, p55 was analyzed by a TransAM TM AP-I kit, or TransAM TM NFkB (Active Motif, CA, USA).
• AGS cells were cultured in a distilled DMEM medium in serum for 24h, then treated with TIL-17A or IL-17F at a concentration of 50 ng / ml for 30 minutes.
• the RNAs were extracted from AGS cells by TRIzol (Invitrogen, USA), and 1 ⁇ g RNA was reverse transcribed using Superscript reverse transcription system (Invitrogen, USA).
• PCR amplification was performed on LightCycler (Roche) using the SYBR Green I Real-time PCR Fast-StartTM DNA Master Kit (Roche Molecular Biochemicals).
• GAPDH has been used as a household gene.
• the C-Jun and GAPDH primers were purchased from Search-LC GmbH (Heidelberg, Germany).
• Thermocycling was carried out starting from a volume of 20 ⁇ l containing the primers at a concentration of 10 ⁇ M, 25 mM of magnesium chloride (MgCl 2), Taq and SYBR Green I dye as recommended in the LightCycler Fast Start DNA Master kit. SYBR green I kit (Roche).
• NM_153460 were obtained from Eurogentec (San Diego, CA): (IL 17RA forward: SEQ ID NoI 5'-AGACACTCCAGAACCAATTCC-3 ', IL17RA reverse : SEQ ID NO: 5'-TCTTAG AGTTGCTCTCCACCA-3 '; IL17RC forward: SEQ ID No35'- ACCAGAACCTCTGGCAAGC-3', IL 17RC reverse: SEQ ID No4 5'-GAGCTGTTCACCTGAACACA-3 '). PCR included 45 amplification cycles (10 seconds at 95 ° C, 10 seconds at 68 ° C and 16 seconds at 72 ° C). The results were expressed by the ratio of target gene / G APDH mRNA.
• Interfering RNA Interfering RNA. Interfering RNAs corresponding to nucleotides 1623-1641 of human IL-17RA (NM 014339) and nucleotides 985-1003 of human IL-17RC (NM 153460) were obtained from Dharmacon (Lafayette, CO, USA). RNAi control was also used ( ⁇ CONTROL). AGS cells (IxIO 5 ) were transfected with 0.5 ⁇ g of IL-17RA RNAi, IL-17RC or RNAi control by the use of a Nucleofector kit (Amaxa GmbH, Cologne, Germany). 24h after transfection, the cells were cultured in serum-depleted medium for 12 h and then treated with 50 ng / ml IL-17A.
• 1TL17A for 24h increased the basal expression of IL8, interleukin involved in neutrophil recruitment, from 604.3 ⁇ 39.2 ⁇ g / ml to 1290.8 ⁇ 142.6 ⁇ g / ml, (P ⁇ 0.05).
• TIL-17A stimulated AGS cells
• the p65 DNA binding activity involved in the development of cancer was 1.6 (p ⁇ 0.05) higher than in the unstimulated cells.
• Stimulation with TIL17F induced induction of p65 (p ⁇ 0.05).
• VIL17-A and F demonstrate that VIL17-A and F, and IL1 7RA and IL1 7RC receptors are therapeutic targets for combating gastric cancer.

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