AR111410A1 - SYNERGIC COMBINATION OF OLIGONUCLEOTIDES OF NUCLEIC ACIDS AND CHEMOTHERAPEUTIC AGENTS INHIBITORS OF PROTEIN KINASES - Google Patents

SYNERGIC COMBINATION OF OLIGONUCLEOTIDES OF NUCLEIC ACIDS AND CHEMOTHERAPEUTIC AGENTS INHIBITORS OF PROTEIN KINASES

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Publication number
AR111410A1
AR111410A1 ARP180100851A ARP180100851A AR111410A1 AR 111410 A1 AR111410 A1 AR 111410A1 AR P180100851 A ARP180100851 A AR P180100851A AR P180100851 A ARP180100851 A AR P180100851A AR 111410 A1 AR111410 A1 AR 111410A1
Authority
AR
Argentina
Prior art keywords
splice variant
nucleic acid
chemotherapeutic agents
gene
protein kinases
Prior art date
Application number
ARP180100851A
Other languages
Spanish (es)
Inventor
Shikha Saini
Fei Yue
Aditi Mathur
Sidney Hopps
Bellur Prabhakar
Original Assignee
Jivana Biotechnology Inc
Univ Illinois
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 Jivana Biotechnology Inc, Univ Illinois filed Critical Jivana Biotechnology Inc
Publication of AR111410A1 publication Critical patent/AR111410A1/en

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    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • C12N2320/30Special therapeutic applications
    • C12N2320/34Allele or polymorphism specific uses

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Abstract

Composiciones y métodos para tratar cánceres, que comprenden administrar una combinación de agentes antineoplásicos, donde la combinación comprende agentes quimioterapéuticos inhibidores de proteína quinasas y una o más moléculas de ácidos nucleicos capaces de regular negativamente la expresión de al menos una variante de empalme del gen IG20, donde no todas las variantes de empalme del gen IG20 son reguladas negativamente. En una forma de realización, la variante de empalme del gen IG20 es una variante de empalme MADD y las moléculas de ácidos nucleicos son siARN, ARNhc y oligonucleótidos antisentido que comprenden una secuencia de ácido nucleico complementaria de la secuencia de ácido nucleico del exón 13L de la variante de empalme MADD o un transcripto de ARNm del exón 13L de la variante de empalme MADD. Métodos para tratar cánceres donde se aplica una terapia combinada con moléculas de ácidos nucleicos capaces de regular negativamente la expresión de al menos una variante de empalme del gen IG20 y agentes quimioterapéuticos inhibidores de proteína quinasas.Compositions and methods for treating cancers, comprising administering a combination of antineoplastic agents, wherein the combination comprises chemotherapeutic agents that inhibit protein kinases and one or more nucleic acid molecules capable of negatively regulating the expression of at least one splice variant of the IG20 gene , where not all splice variants of the IG20 gene are negatively regulated. In one embodiment, the splice variant of the IG20 gene is a MADD splice variant and the nucleic acid molecules are siRNA, hRNA and antisense oligonucleotides comprising a nucleic acid sequence complementary to the exon 13L nucleic acid sequence of the MADD splice variant or an exon 13L mRNA transcript of the MADD splice variant. Methods to treat cancers where a combination therapy with nucleic acid molecules capable of negatively regulating the expression of at least one splice variant of the IG20 gene and protein kinase inhibitor chemotherapeutic agents is applied.

ARP180100851A 2017-04-24 2018-04-05 SYNERGIC COMBINATION OF OLIGONUCLEOTIDES OF NUCLEIC ACIDS AND CHEMOTHERAPEUTIC AGENTS INHIBITORS OF PROTEIN KINASES AR111410A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201762489050P 2017-04-24 2017-04-24

Publications (1)

Publication Number Publication Date
AR111410A1 true AR111410A1 (en) 2019-07-10

Family

ID=63919941

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP180100851A AR111410A1 (en) 2017-04-24 2018-04-05 SYNERGIC COMBINATION OF OLIGONUCLEOTIDES OF NUCLEIC ACIDS AND CHEMOTHERAPEUTIC AGENTS INHIBITORS OF PROTEIN KINASES

Country Status (3)

Country Link
AR (1) AR111410A1 (en)
TW (1) TW201902487A (en)
WO (1) WO2018200149A1 (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004012769A1 (en) * 2002-08-02 2004-02-12 The Regents Of The University Of California Therapeutic inhibitionof protein kinases in cancer cells
WO2007084954A2 (en) * 2006-01-19 2007-07-26 The Board Of Trustees Of The University Of Illinois Selective inhibition of ig20 splice variants to treat cancers
WO2010006239A2 (en) * 2008-07-10 2010-01-14 The Board Of Trustees Of The University Of Illinois Regulation of apoptosis by neural specific splice variants of ig20

Also Published As

Publication number Publication date
WO2018200149A1 (en) 2018-11-01
TW201902487A (en) 2019-01-16

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