Acid Ceramidase, Target for Cancer

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$441,419.00
Award Year:
2009
Program:
STTR
Phase:
Phase I
Contract:
1R41CA139637-01
Award Id:
93528
Agency Tracking Number:
CA139637
Solicitation Year:
n/a
Solicitation Topic Code:
n/a
Solicitation Number:
n/a
Small Business Information
2114 VASI COURT, MOUNT PLEASANT, SC, 29466
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
189978245
Principal Investigator:
XIANG LIU
() -
LIUX@MUSC.EDU
Business Contact:
JAMES NORRIS
() -
norrisjs@musc.edu
Research Institution:
MEDICAL UNIVERSITY OF SOUTH CAROLINA

Office of Research and Sponsored Programs
19 Hagood Ave., Suite 606
CHARLESTON, SC, 29425 6203

Nonprofit college or university
Abstract
DESCRIPTION (provided by applicant): Acid ceramidase (AC) has been implicated as a novel target for cancer therapy because of its pivotal role in regulating interconversion of three key bioactive lipids; ceramide (Cer), sphingosine (Sph) and Sphingosine-1- Phosphate (S1P). It is well known that Cer functions predominantly as a tumor suppressor lipid and mediator of apoptosis following chemo and radio therapy. On the other hand, S1P is a tumor promoting lipid that counteracts the actions of Cer. Importantly, our recent studies identified AC as a negative prognostic factor in cancer therapy, since AC over-expression induces a more aggressive cancer phenotype which causes drug or radiation resistance. Reversal of AC expression utilizing siRNA or small molecule A C inhibitors clearly demonstrated a reduction in the aggressive cancer phenotype and improved chemo, gene or radiation therapy outcomes in vitro and in vivo. Up-regulated AC expression has been observed in 60-70% of cancers examined including in breast, lu ng, prostate, melanoma, colon, brain, and oral cancers. New cases per year totaling more than 700,000 patients are projected from these data based on ACS 2004 statistics. Thus, because of the potential for a direct benefit of improved clinical outcomes, th e development of small molecule AC inhibitors by SphingoGene, Inc. is a commercially feasible proposition. Therefore, the goal of this phase I STTR application is to develop and validate targeted AC inhibitors. To achieve this goal the following specific a ims will be carried out. Aim 1: Rationally design and synthesize N-alkylamino-prodrugs (Class E) that inhibit AC enzyme activity. Aim 2: Determine activity of Class E compounds in vitro and at the cellular level. Aim 3: Determine in vivo toxicity, pharmaco kinetics/pharmacodynamics and AC inhibitory activity of lead Class E1 and E2-5 AC inhibitors. This research is a partnership between basic scientists at MUSC and SphingoGene, Inc. Drugs developed in this program will have a direct clinical application in c ancer therapy. PUBLIC HEALTH RELEVANCE: The data generated by this grant may lead to a direct clinical application. This grant proposes to develop a new class of acid ceramidase inhibitors. These inhibitors function by modifying sphingolipid metabolism and facilitating the effect of chemo, radiation or gene therapy in killing cancer cells.

* information listed above is at the time of submission.

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