SBIR/STTR Research Award

Anti-cancer Drig Sensitizers

Award identifier b2ee87b79074fb5862a1be659d7051d4990a2b04d22e4903b4698ebf7b323be8Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$135,800

Program and phase

SBIR · Phase I

Award year

2008

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
QUATROS RESEARCH AND DEVELOPMENT, LLC
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2007-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): One aspect of conventional chemotherapy that often results in failure is the development of drug resistance through increased efficiency by the cancer cell in pumping drugs out of the cell, which is an energy requiring process. Many cancer cells, including breast cancer cells, have converted to aerobic glycolysis as the main source of ATP energy, suggesting that selective interference with glycolytic production of ATP in cancer cells may render these cells less able to p ump out chemotherapeutic drugs. Many tumors selectively up-regulate the expression of lactate dehydrogenase A4 (LDH-A). This leads to the HYPOTHESIS: Selective LDH-A inhibitors will provide an ATP-depleting strategy to sensitize breast cancer cells to adju vant chemotherapy. SPECIFIC AIM: The applicant proposes to carry out an animal study of the effectiveness of inhibitors of human lactate dehydrogenase A4 (LDH-A) as sensitizers of conventional adjuvant cancer chemotherapy against breast cancer. The compoun ds that will be tested include the natural product gossypol, gossypol derivatives such as gossylic lactone and gossypol analogs, all of which are inhibitors of LDH-A. The phase 1 goals of this study are: 1) to demonstrate that treatment of the murine EMT- 6 mammary carcinoma cell with the above compounds decreases ATP production in vitro; and 2) to use this cell which is syngeneic to the Balb/c mouse as a mammary carcinoma tumor model to investigate tumor growth delay as an in vivo proof of principal that i nhibition of ATP production will increase the sensitivity of tumor growth to standard chemotherapy with cyclophosphomide and 5-fluorouracil. Breast cancer remains the most common non-cutaneous cancer among US women. The most common treatments, either maste ctomy or breast-conserving surgery combined with radiation, are often followed by systemic adjuvant therapies such as adjuvant hormone therapy or adjuvant chemotherapy to aid in prevention of recurrence. The goal of radiation or chemotherapy is to kill can cer cells with as much selectivity as possible. Cancer cells often become resistant to chemotherapy by pumping the drugs out of the cell, which requires energy. The question is whether cancer cells can be made more sensitive to existing drugs, which would extend the use of available therapies. Since most cancer cells have switched to glycolysis for energy production, cancer cells should be especially sensitive to inhibition of glycolysis. This research project will test whether compounds that are known to i nhibit glycolysis will sensitize breast cancer cells to treatment with widely used chemotherapeutic drugs. The research will utilize an accepted animal model of mammary cancer to address this question.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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