US2010092578A1PendingUtilityA1
Protein kinase c iota
Individually held — no corporate assignee on recordPriority: Mar 8, 2004Filed: Oct 1, 2009Published: Apr 15, 2010
Est. expiryMar 8, 2024(expired)· nominal 20-yr term from priority
A01K 2217/052G01N 2500/02C12N 15/8509C12N 9/1205C12N 2830/008A01K 2227/105G01N 2333/91215A61P 35/00A01K 2267/0331A01K 67/0278G01N 33/5752G01N 33/57535
40
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Claims
Abstract
The invention involves PKC ι signaling. The invention provides, for example, transgenic animals, inhibitors of PKC ι signaling, methods for inhibiting PKC ι signaling, methods for identifying inhibitors of PKC ι signaling, and methods for diagnosing cancer.
Claims
exact text as granted — not AI-modified1 . A method for inhibiting a protein kinase C iota polypeptide response in a mammal, said method comprising administering an inhibitor to said mammal under conditions wherein said response is inhibited, wherein said inhibitor reduces the interaction between a protein kinase C iota polypeptide and a polypeptide selected from the group consisting of Par-6, Src, Par-4, p62/ZIP, and Par-3 polypeptides.
2 . The method of claim 1 , wherein said response is cell transformation, development of cancer, or colon carcinogenesis.
3 . The method of claim 1 , wherein said inhibitor is a polypeptide fragment.
4 . The method of claim 3 , wherein said polypeptide fragment comprises an amino acid sequence present in said protein kinase C iota polypeptide.
5 . The method of claim 1 , wherein said inhibitor is aurothioglucose, aurothiomaleate, thimerosal, phenylmercuric acetate, ebselen, cisplatin, apomorphine, pyrantel pamoate, gossypol-acetic acid complex, ellagic acid, or hexestrol.Join the waitlist — get patent alerts
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