US2019233484A1PendingUtilityA1
Kidney disease targets and uses thereof
Est. expiryMar 25, 2025(expired)· nominal 20-yr term from priority
A61P 35/00C07K 2317/734C12Q 1/6876C07K 2317/622C07K 16/3038Y10T436/143333C12Q 2600/118C07K 14/435C12Q 2600/158G01N 2333/47G01N 2500/00C12N 2310/14C12Q 2600/136G01N 2500/10A61P 13/12A61K 2039/505C12N 15/113C07K 2317/92C07K 2317/73C12Q 1/6886C07K 14/47G01N 33/53C07K 16/18C07K 2317/732G01N 33/57525G01N 33/5758G01N 33/57438G01N 33/57484
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Claims
Abstract
The present invention provides a method for diagnosing and detecting diseases associated with kidney. The present invention provides one or more proteins or fragments thereof, peptides or nucleic acid molecules differentially expressed in kidney diseases (KCAT) and antibodies binds to KCATs. The present invention provides that KCATs are used as targets for screening agents that modulates the KCAT activities. Further the present invention provides methods for treating diseases associated with kidney.
Claims
exact text as granted — not AI-modified1 . An isolated protein comprising an amino acid sequence selected from the group consisting of SEQ ID NOS:1-2736 and 5165-6044.
2 . A composition comprising the protein of claim 1 and a pharmaceutically acceptable carrier.
3 . An isolated nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of:
a) SEQ ID NOS:2737-5164; b) nucleotide sequences that encode a protein comprising an amino acid sequence selected from the group consisting of SEQ ID NOS:1-2736 and 5165-6044; and c) nucleotide sequences that are completely complementary to the nucleotide sequences of a) or b).
4 . An isolated RNAi or antisense nucleic acid molecule that selectively binds to the nucleic acid molecule of claim 3 .
5 . An isolated antibody that selectively binds to the protein of claim 1 .
6 . The antibody of claim 5 , wherein the antibody is at least one of a monoclonal, polyclonal, fully human, humanized, chimeric, single-chain, or anti-idiotypic antibody.
7 . A cell line, hybridoma, phage, or transgenic organism that produces the antibody of claim 5 .
8 . The antibody of claim 5 , wherein the antibody is coupled to a composition selected from the group consisting of detectable substances and therapeutic agents.
9 . A composition comprising the antibody of claim 5 and a pharmaceutically acceptable carrier.
10 . An isolated antibody fragment of the antibody of claim 5 , wherein the antibody fragment comprises a fragment selected from the group consisting of:
a) an Fab fragment; b) an F(ab′) 2 fragment; and c) an Fv fragment.
11 . A method of modulating cell proliferation or apoptosis, the method comprising contacting a cell with the antibody of claim 5 .
12 . The method of claim 11 , wherein the method comprises either inhibiting proliferation of kidney cancer cells or stimulating apoptosis of kidney cancer cells.
13 . A method of modulating cell proliferation or apoptosis, the method comprising contacting a cell with the RNAi or antisense nucleic acid molecule of claim 4 .
14 . A method of detecting the protein of claim 1 in a sample, the method comprising contacting the sample with an isolated antibody that selectively binds to the protein and determining whether the antibody binds to the protein.
15 . A method of detecting the nucleic acid molecule of claim 3 in a sample, the method comprising contacting the sample with an oligonucleotide that specifically hybridizes to the nucleic acid molecule and determining whether the oligonucleotide binds to the nucleic acid molecule.
16 . A method of diagnosing, prognosing, or determining risk of kidney cancer in a subject, the method comprising detecting at least one molecule in a sample, wherein the presence or abundance of the molecule is indicative of kidney cancer, and wherein the molecule is selected from the group consisting of:
a) proteins comprising an amino acid sequence selected from the group consisting of SEQ ID NOS:1-2736 and 5165-6044; b) antibodies that selectively bind to the protein of a); c) nucleic acid molecules comprising a nucleotide sequence selected from the group consisting of SEQ ID NOS:2737-5164 and nucleotide sequences that encode the protein of a); and d) nucleic acid molecules comprising a nucleotide sequence that is completely complementary to the nucleic acid molecule of c).
17 . A method of treating kidney cancer, the method comprising administering a therapeutically effective amount of the antibody of claim 5 to a subject.
18 . A method of screening agents, the method comprising contacting the protein of claim 1 or a cell that expresses the protein with an agent, and assaying for whether the agent binds to the protein or modulates the function, activity, or expression of the protein.
19 . A composition comprising the agent identified by the method of claim 18 and a pharmaceutically acceptable carrier.
20 . A method of determining or predicting the effectiveness of a treatment or selecting a treatment for administration to a subject having kidney cancer, the method comprising detecting the presence, abundance, or activity of the protein of claim 1 in a sample and determining or predicting the effectiveness of the treatment or selecting the treatment for administration based on the presence, abundance, or activity of the protein.Cited by (0)
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