IP Library Granted Patent US 8,216,782
Granted Patent B2
US 8,216,782 · App. 12/867,042 · Granted Jul 10, 2012

PTTG1 as a biomarker for cancer treatment

Assignee: Cedars-Sinai Medical Center
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,216,782
App. No.
12/867,042
Granted
Jul 10, 2012
Kind
B2
Abstract

The present invention relates to the use of pituitary tumor transforming gene 1 (PTTG1) as a biomarker for diagnosing cancer as well as for determining cancer treatment responsiveness. In one embodiment, the present invention provides a method of treating cancer by inhibiting the expression of PTTG1, and administering a therapeutically effective amount of Aurora kinase inhibitor, HDAC inhibitor and/or ROS-generating agent.

Claims (9)

1. A method of predicting the sensitivity of a cancer cell to a chemotherapeutic agent, comprising:

identifying the presence or absence of an upregulation of pituitary tumor transforming gene (PTTG1) in the cancer cell relative to a normal non-cancerous cell, and

predicting that the cancer cell lacks sensitivity to the chemotherapeutic agent if upregulation of PTTG1 is present.

2. The method of claim 1 , wherein identifying the presence of an upregulation of PTTG1 comprises detecting a level of PTTG1 activity that is at least approximately twice the level found in a normal non-cancerous cell.

3. The method of claim 1 , wherein the cancer cell is a HCT116 cell.

4. The method of claim 1 , wherein the chemotherapeutic agent comprises an Aurora kinase inhibitor, a histone deacetylase (HDAC) inhibitor and/or a reactive oxygen species (ROS) generating agent.

5. The method of claim 4 , wherein the Aurora kinase inhibitor is Aurora Kinase Inhibitor II or Aurora Kinase Inhibitor III.

6. The method of claim 4 , wherein the HDAC inhibitor is trichostatin A (TSA) or suberoylanilide hydroxamic acid (SAHA).

7. The method of claim 4 , wherein the ROS-generating agent is H 2 O 2 or phenethyl isothiocyanate (PEITC).

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 17, 2013
From: CEDARS-SINAI MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031288/0098 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 10, 2010
From: TONG, YUNGUANG; MELMED, SHLOMO
To: CEDARS-SINAI MEDICAL CENTER
Reel/Frame 024817/0895 →
Continuity (3)
Provisional Application 61036524 · Mar 14, 2008
Provisional Application 61147435 · Jan 26, 2009
Related Publication 20110009473A1 · Jan 13, 2011