SBIR/STTR Research Award
Treating Cancer of the GI using Cryomolecular Biology
Award amount
$100,000Program and phase
SBIR · Phase IAward year
2001Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- CRYOMEDICAL SCIENCES, INC.
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
DESCRIPTION (provided by applicant): Cryomedical Sciences Inc. (CMSI) teamed
with the University of Texas Medical Center and Johns Hopkins Medical Center
proposes to develop cryosurgical procedures for the treatment of
gastrointestinal (GI) cancers. This Phase 1 study will focus on molecular
biological studies and development of prototype cryosurgical devices; whereas
the Phase II work will focus on the application of these endoscopic
cryosurgical devices in a canine model. CMSI recognizes a need to explore the
molecular biological mechanisms of cell death that occur as a consequence of
hypothermic(15 to 4C) and freezing (0C to -196C) episodes. CMSI is using
molecular biological research to develop improved cryosurgical protocols
through an understanding freeze-related cell death and survival. Data from
cryosurgeons in the past few years have indicated that cancer cells in the
middle of a tissue iceball created during cryosurgical procedures die
immediately due to necrosis; whereas many of the cells that die in the iceball
periphery where temperatures approach 0C die several days subsequent to
cryoablation. While some of the peripheral cells survive the freezing insult.
In vitro and molecular genetic studies performed at CMSI show that cells frozen
at -70C die by necrosis; whereas at least 25 percent of the cells that die at
-15C succumb via apoptosis. These observations lead to CMSI's in vitro
cryochemo adjunct therapy studies showing that the addition of non-toxic levels
of the apoptosis initiator 5-fluorouracil (5-FU) to kidney, liver, prostate and
most notably colon cancer cells enhances the efficacy of cryoablation. This
Phase I grant will determine if (1) sub-lethal freezing of HT-29 and/or Caco-2
colon carcinoma cells results in the increase in synthesis of the cell death
regulators, bcl-2, bax, Apaf 1, FADD, Fas and PARP; (2) sublethal freezing
causes an up-regulation of caspase mRNA levels; (3) cell death due to freezing
injury is cell cycle phase dependent and (4) modifications can be made to two
prototype cryosurgical devices that are currently being designed for treating
Barrett's esophagus and colon cancer to make them more useful and efficacious
in the cryosurgical suite.
PROPOSED COMMERCIAL APPLICATION: NOT AVAILABLE
Technology keywords
Not reported