SBIR/STTR Research Award

Injectable microgel for soft tissue repair

Award identifier 080e7e9eb1e98d7393c094aca8a9e6381ff1861483566b55198072a2974ad651Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$280,492

Program and phase

SBIR · Phase I

Award year

2013

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
DAYSAI BIOPHARMACEUTICALS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PA12-088
Topic code
NCI

Research abstract

DESCRIPTION (provided by applicant): BCL6 is the most commonly involved oncogene in B-cell lymphomas, and is expressed constitutively in a majority of patients with the two most frequent forms of lymphoma: the diffuse large B-cell lymphomas (DLBCL) and follicular lymphoma (FL). Many of these BCL6 positive tumors require the continued presence of BCL6 in order to maintain their survival. BCL6, a member of the BTB/POZ family of transcriptional repressors, mediates its effects on gene silencing through recruitment of the SMRT, N- CoR and BCoR corepressor proteins. The BTB domain of BCL6 provides an extended groove-like surface to which a linear peptide from the SMRT, N-CoR and BCoR corepressor can bind with high affinity. This protein-protein interaction is required for BCL6 to repress critical checkpoint regulatory genes such as ATR and TP53. We hypothesize that drugs designed to occlude the BCL6 BTB domain corepressor binding groove will block the ability of BCL6 to repress its critical target genes and forcelymphoma cells to undergo programmed cell death. This proposal brings together expertise in computer-aided drug design, medicinal chemistry, structural biology and lymphoma biology to identify and optimize low molecular weight chemical compounds that disrupt the ability of BCL6 to recruit corepressors through the BTB lateral groove and determine the therapeutic efficacy of BCL6 small molecule inhibitors in B-cell lymphomas in vitro and in vivo. In preliminary data this team has already demonstrated the ability to generate specific BCL6 inhibitors that are able to block BCL6 activities and kill DLBCLs in vitro and in vivo. The proposed methodology will build on this success by performing more advanced forms of computer aided drug design, and using functionaland structural information obtained through multiple methods. The expected outcome is the development of several chemical structures with nanomolar affinity for BCL6, favorable drug-like properties and potent therapeutic efficacy. PUBLIC HEALTHRELEVANCE PUBLIC HEALTH RELEVANCE: B-cell lymphomas are the fourth most common form of cancer in the United States and several subtypes of this disease are incurable. The most common causative oncogene in these tumors is the BCL6 transcriptional repressorprotein. This proposal will develop drugs that specifically target BCL6, which we predict will have a major impact on improving the clinical care for patients with B-cell lymphomas.

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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