The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 07, 2017

Filed:

Mar. 10, 2014
Applicant:

Board of Regents, the University of Texas System, Austin, TX (US);

Inventors:

Usha R. Pendurthi, Tyler, TX (US);

Vijaya M. R. Lella, Tyler, TX (US);

Shivakeshava Gaddam, Tyler, TX (US);

Steven Idell, Tyler, TX (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 38/17 (2006.01); A61K 48/00 (2006.01); C12N 15/113 (2010.01); A61K 9/00 (2006.01); A61K 31/4439 (2006.01); A61K 31/5377 (2006.01); A61K 38/19 (2006.01); A61K 38/21 (2006.01);
U.S. Cl.
CPC ...
A61K 38/177 (2013.01); A61K 9/007 (2013.01); A61K 9/0019 (2013.01); A61K 31/4439 (2013.01); A61K 31/5377 (2013.01); A61K 38/191 (2013.01); A61K 38/217 (2013.01); A61K 48/005 (2013.01); A61K 48/0058 (2013.01); C12N 15/113 (2013.01); C12N 2310/14 (2013.01); C12N 2310/531 (2013.01); C12N 2710/10343 (2013.01); C12N 2710/10371 (2013.01);
Abstract

The influence of TF, endothelial cell protein C receptor (EPCR) and protease activated receptor-1 (PAR1) on tumor growth of malignant pleural mesothelioma (MPM) is disclosed. MPM cells that lack or express TF, EPCR or PAR1 and a murine orthotopic model of MPM led to the discovery that intrapleural administration into nude mice of REN MPM cells expressing TF and PAR1 but lacking EPCR and PAR2 generated large pleural cavity tumors. Suppression of TF or PAR1 expression markedly reduced tumor growth. Overexpression of TF in non-aggressive MPM cells expressing EPCR and PAR1 but exhibiting minimal levels of TF failed to alter their tumorigenicity. Introduction of EPCR expression in aggressive MPM cells attenuated tumor growth whereas EPCR silencing in non-aggressive MPM cells overexpressing TF increased tumorigenicity of non-aggressive cells. Expression of EPCR by MPM cells suppresses tumor growth and treats MPM.


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