SBIR/STTR Research Award

Targeting S1P3 for the Treatment of Breast Cancer

Award identifier 3047ade98a977322fdb0d9c46a2d7d615e880ef28721c50163e471f7ea57119bAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$100,000

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
EXPRESSION DRUG DESIGN LLC
Proposal award date
Not reported
Contract end date
Not reported
UEI
KLATKA5XJYG3
Solicitation number
PHS2007-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Breast cancer is a physically and emotionally devastating diagnosis affecting over 2.3 million Americans living with the disease and killing over 100 women each day. Although the prognosis for this disease is gradually improving with the development of chemotherapeutic drugs, many aggressive forms of breast cancer are resistant to chemotherapy and result in a 10% mortality rate within 5 years of diagnosis. A compound known as sphingosine 1-phosphate (S1P) may be a major determinant of the aggressiveness and drug resistance of breast cancer. S1P is a small molecule normally present in high concentrations in the blood that accelerates the progression of breast cancer. It does this by promoting the growth and spreading of ca ncer cells and by stimulating the formation of new blood vessels, thereby increasing the supply of oxygen and nutrients to the tumor. Evidence suggests that these actions are largely the result of the stimulation of a specific receptor for S1P called S1P3. Since S1P has been shown to be a general growth stimulant for breast cancer cells, and since it causes normal blood vessels to grow uncontrollably in tumors, it is likely that inhibiting S1P3 will slow the progression of most forms of breast cancer and se nsitize the tumors to treatment with conventional chemotherapy. Animal studies suggest that loss of this receptor is not associated with undesirable effects, providing evidence for the safety of this approach. However, there are currently no reports of any drug compounds that specifically block S1P3. Successful completion of the proposed project will 1) characterize the potential clinical relevance of targeting S1P3, and 2) use an innovative and versatile technology to produce drug candidates. It is likely that these drug candidates will ultimately result in a new breast cancer treatment that will increase the effectiveness of chemotherapy while reducing the often debilitating side effects associated with these drugs. PUBLIC HEALTH RELEVANCE:Breast cancer is the most common form of cancer in the U.S. causing the death of over 35,000 American women each year. Much of this mortality can be averted by increasing the effectiveness and reducing the side effects of conventional chemotherapy. The proposed research w ill develop a drug specifically designed to interrupt cellular processes known to promote growth of breast tumors, thus limiting cancer growth and improving the effectiveness of chemotherapy at lower doses.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Research funding history

4 SBIR/STTR records share this UEI (2008–2011). Reported award amounts total $1,627,992. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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