IP Library Granted Patent US 11,366,100
Granted Patent B2
US 11,366,100 · App. 15/116,319 · Granted Jun 21, 2022

P13K-MTORC1-S6K1 signaling pathway biomarkers predictive of anti-cancer responses

Inventors: Thomas M. Roberts (Cambridge, MA); Haoxuan Tong (Cambridge, MA); Jean Zhao (Brookline, MA); John Blenis (New York, NY)
Assignees: Dana-Farber Cancer Institute, Inc.; President and Fellows of Harvard College
G01N33/5011A61K31/58A61K45/06C12Q1/6886G01N33/5088G01N33/57492C12Q2600/106C12Q2600/118C12Q2600/136C12Q2600/156C12Q2600/158G01N2333/91215G01N2500/10
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Quick Facts
Patent No.
US 11,366,100
App. No.
15/116,319
Granted
Jun 21, 2022
Kind
B2
Abstract

The present invention is based, in part, on the identification of novel FI.3K-mTORCI-S6K 1 signaling pathway biomarkers predictive of responsiveness to anti-cancer therapies.

Claims (6)

1. A method of treating a human subject afflicted with T cell acute lymphoblastic leukemia characterized by reduced Pten function and amplification or overexpression of a c-Myc transcript comprising a 5′-untranslated region (5′-UTR) relative to a normal control, comprising administering to the subject an inhibitor of eukaryotic initiation factor-4A (eIF4A) and/or an inhibitor of eukaryotic initiation factor-4B (eIF4B), wherein the inhibitor is selected from the group consisting of RNA interference-mediating nucleic acids that bind eIF4A or eIF4B, hippuristanol, pateamine A, silvestrol, and rocaglamides, thereby treating the subject.

2. The method of claim 1 , wherein

i) the efficacy of the treatment is measured by at least one criteria selected from the group consisting of clinical benefit rate, survival until mortality, pathological complete response, semi-quantitative measures of pathologic response, clinical complete remission, clinical partial remission, clinical stable disease, recurrence-free survival, metastasis free survival, disease free survival, circulating tumor cell decrease, circulating marker response, and RECIST criteria; and/or

ii) the inhibitor of eIF4A and/or eIF4B is administered in a pharmaceutically acceptable formulation.

3. The method of claim 1 , wherein the eIF4A and/or eIF4B is selected from the group consisting of human eukaryotic initiation factor-4A (eIF4A) or an ortholog thereof, and human eukaryotic initiation factor-4B (eIF4B) or an ortholog thereof.

4. The method of claim 1 , further comprising administering one or more additional anti-cancer agents.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 14, 2019
From: BLENIS, JOHN
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 051006/0742 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 14, 2019
From: ROBERTS, THOMAS M.; TONG, HAOXUAN; ZHAO, JEAN
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 051006/0785 →
CONFIRMATORY LICENSE Recorded Jun 26, 2017
From: DANA-FARBER CANCER INSTITUTE
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 042992/0117 →
CONFIRMATORY LICENSE Recorded Sep 28, 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 040181/0160 →
Continuity (2)
Provisional Application 61938816 · Feb 12, 2014
Related Publication 20170184565A1 · Jun 29, 2017