US2013331294A1PendingUtilityA1

Egfr/nedd9/tgf-beta interactome and methods of use thereof for the identification of agents having efficacy in the treatment of hyperproliferative disorders

Assignee: FOX CHASE CANCER CTPriority: Nov 9, 2007Filed: Jul 15, 2013Published: Dec 12, 2013
Est. expiryNov 9, 2027(~1.3 yrs left)· nominal 20-yr term from priority
G01N 33/57545G01N 33/57525G01N 33/57515G01N 33/5752G01N 33/575G01N 33/502C12Q 1/6886C12Q 2600/136C12Q 2600/178C12Q 2600/158G01N 33/5044
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Claims

Abstract

Compositions and methods for the treatment and diagnosis of cancer are disclosed.

Claims

exact text as granted — not AI-modified
1 - 30 . (canceled) 
     
     
         31 . A method for determining whether a patient will respond to EGFR/MEK-1 targeting therapy, comprising
 a) isolating cancer cells from said patient;   b) determining expression levels of biomarkers listed in Table 2;   c) contacting said cells with an agent that targets EGFR/MEKL-1; and   d) determining whether said agent is effective to alter the biomarker expression levels determined in step b).   
     
     
         32 . The method of  claim 31 , wherein said cancer is selected from the group consisting of colorectal cancer, HNSCC, lung cancer, pancreatic cancer, glioma, breast cancer and ovarian cancer. 
     
     
         33 . The method of  claim 31 , wherein said biomarkers comprise one or more markers selected from the group consisting of ANXA6, ARF4, ARF5, ASCL2, CD59, DIXDC1, DUSP4, DUSP6, DUSP7, FER, MATK, NEDD9, PRIAP19/SLP1, PRKACB, RAPGEF1, SC4MOL and SH2DC3. 
     
     
         34 . The method of  claim 31 , wherein said agent causes a cellular phenotype selected from the group consisting of morphological alterations, altered migratory properties, altered levels of apoptosis, altered angiogenic properties, and altered chromosomal or DNA integrity.

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