IP Library Granted Patent US 10,378,060
Granted Patent B2
US 10,378,060 · App. 14/350,164 · Granted Aug 13, 2019

ZNF365/ZFP365 biomarker predictive of anti-cancer response

Inventors: Ronald A. DePinho (Houston, TX); Ji-Hye Paik (New York, NY)
Assignee: Dana-Farber Cancer Institute, Inc.
C12Q1/6886A61K31/4184A61N5/10G01N33/57496C12Q2600/106C12Q2600/156
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Quick Facts
Patent No.
US 10,378,060
App. No.
14/350,164
Granted
Aug 13, 2019
Kind
B2
Abstract

The present invention is based on the identification of novel biomarkers predictive of response to anti-cancer therapies.

Claims (11)

1. A method of inhibiting the proliferation of breast cancer cells having less than a diploid copy number of ZNF365 in a human subject, the method comprising administering an inhibitor of PARP-1 and/or PARP-2 to a human subject determined to have less than a diploid copy number of ZNF365 n breast cancer cells, wherein the determination is achieved by:

a) measuring the copy number of ZNF365 in a test sample comprising breast cancer cells; and

b) determining that a less than diploid copy number of ZNF365 is present in the breast cancer cells in the test sample.

2. The method of claim 1 , wherein ZNF365 encodes a protein that reduces DNA repair activity.

3. The method of claim 2 , wherein the DNA repair activity is selected from the group consisting of non-homologous end joining, homologous recombination, and DNA single-strand break repair.

4. The method of claim 2 , wherein the protein encoded by ZNF365 interacts with a protein selected from the group consisting of PARP-1, PARP-2, DNA-PK, Ku70, MRE11, RPA, CHEK1, and a topoisomerase.

5. The method of claim 1 , wherein ZNF365 encodes a protein having an amino acid sequence selected from the group consisting of SEQ ID NOs: 2, 4, 6, and 8.

6. The method of claim 1 , wherein the breast cancer cells harbor defects in genes encoding proteins mediating non-homologous end joining, homologous recombination, or DNA single-strand break repair.

7. The method of claim 6 , wherein the breast cancer cells harbor defects in BRCA1, BRCA2, and/or Fanconi anemia (FANC) genes.

8. The method of claim 1 , further administering chemotherapy, radiation therapy, or a combination of chemotherapy and radiation therapy, wherein said chemotherapy does not target PARP-1 and/or PARP-2.

9. The method of claim 8 , wherein the chemotherapy comprises inhibitors selected from the group consisting of inhibitors of DNA-PK, Ku70, MRE11, RPA, CHEK1, and topoisomerases.

Assignments (3)
CONFIRMATORY LICENSE Recorded Sep 23, 2016
From: DANA-FARBER CANCER INST
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040129/0173 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S NAME PREVIOUSLY RECORDED ON REEL 033556 FRAME 0837. ASSIGNOR(S) HEREBY CONFIRMS THE SPELLING OF DAN-FARBER SHOULD BE DANA-FARBER. Recorded Aug 25, 2014
From: DEPINHO, RONALD A.; PAIK, JI-HYE
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 033605/0738 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 18, 2014
From: DEPINHO, RONALD A.; PAIK, JI-HYE
To: DAN-FARBER CANCER INSTITUTE, INC
Reel/Frame 033556/0837 →
Continuity (2)
Provisional Application 61547212 · Oct 14, 2011
Related Publication 20140235686A1 · Aug 21, 2014
Cited By (1)
US 12,245,355