SBIR/STTR Research Award
UNIQUE THIOREDOXIN INHIBITORS AS ANTI-CANCER DRUGS
Award amount
$188,860Program and phase
SBIR · Phase IAward year
2001Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- PROLX PHARMACEUTICALS CORPORATION
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
DESCRIPTION: ProlX Pharmaceutical has demonstrated that thioredoxin has an
important role in maintaining the transformed phenotype of some human cancers
as well as their resistance to chemotherapeutic drugs and is thus a highly
rational target for novel cancer drug development. The studies described
herein, suggest that thioredoxin is a human anti apoptosis and oncogene that is
overexpressed by a number of human cancers. ProlX has exclusive worldwide
rights to develop the thioredoxin target and is dedicated to exploiting these
observations and rapidly developing agents that selectively disrupt this novel
signal transduction pathway. The objective of this Phase I proposal is to
develop novel inhibitors of thioredoxin redox system based on a new
pharmacophore, identified from the NCI database using ProlX lead compound
activities in the 60 cell lines screen and the COMPARE analyses. The Specific
Aims of the proposal are 1) to synthesis selective inhibitors of the
thioredoxin system using combinatorial chemistry for lead optimization; 2) to
investigate the specificity of the compounds for thioredoxin/thioredoxin
reductase signaling in vitro; and 3) to evaluated the most active analogues for
anti-tumor activity in vivo. These studies will provide novel lead anticancer
candidates for further preclinical development, including toxicology,
pharmacokinetic studies and the eventual Phase I clinical trial, which will be
the subject of a future Phase II application.
PROPOSED COMMERCIAL APPLICATION:
One is every four deaths in the US is doe to cancer. The overall cancer drug market exceeds
$2 billion in the USA. There is significant need to identify novel and selective small molecule-
based cancer therapies. This proposal seeks to undertake the synthesis of a chemical library
of thioether analogues as potential anticancer drugs, which through thioredoxin inhibition
would provide novel therapies against breast, lung, colon and gastric cancer, all which
have been found to have elevated thioredoxin levels.
Technology keywords
Not reported