Small cell lung cancer (SCLC) is an aggressive neuroendocrine cancer that accounts for approximately 16% of new lung cancer diagnoses. Though SCLC is initially responsive to cytotoxic chemotherapy, resistance quickly develops, with 5-year survival rates below 7%, a prognosis that has not improved significantly over the past 30 years. ASCL1 is present in a majority of human-derived SCLC cell lines and, where tested, is required for tumor cell growth. This proneural basic helix-loop-helix (bHLH) transcription factor normally regulates neuronal differentiation during embryonic development. Its requirement in SCLC suggests that strategies to inhibit the function of this transcription factor may represent a novel, targeted SCLC therapy. Proneural bHLH transcription factors, including ASCL1, have a defined lifetime during embryonic development. It has been proposed that proneural bHLH transcription factors are regulated by phosphorylation of a serine residue at a conserved position within the bHLH domain. Phosphorylation at this site has been suggested to function as a switch that rapidly shuts off the activity of ASCL1, overcoming an autoregulatory positive feedback loop that sustains the proliferative capacity of ASCL1 expressing cells. Interestingly, ASCL1 does not appear to be phosphorylated at this site in SCLC. I hypothesize that the phosphorylation of ASCL1 at this conserved site can be induced to inactivate this oncogenic driver in the context of SCLC. The current proposal will test this hypothesis by determining the effect of phosphorylation at this conserved site on the transcriptional activity, DNA binding, and heterodimerization capacity of ASCL1. In addition, I will test whether phosphorylation of ASCL1 at this conserved site can be invoked in SCLC to inhibit tumor growth by replacing wild-type ASCL1 with phosphomimetic variants both in vitro and in vivo. Finally, in vitro phosphorylation assays will be performed with several kinases predicted to phosphorylate ASCL1 at this site, to test the ability of candidate kinase agonists to disrupt SCLC growth both in vitro and in vivo. These experiments have the potential to identify a novel, mechanism-based therapy for this treatment resistant cancer.

Public Health Relevance

ASCL1, a proneural basic helix-loop-helix (bHLH) transcription factor that regulates neuronal differentiation during embryonic development, is required for the growth of a majority of small cell lung cancers (SCLC), a group of aggressive neuroendocrine cancers with a dismal 5-year survival rate. It has been suggested that during embryonic development, the activity of proneural bHLH transcription factors, including ASCL1, is rapidly shut off by phosphorylation of a specific conserved serine residue that is not phosphorylated in SCLC, suggesting that induced phosphorylation at this site may be exploited to inactivate this transcription factor. This proposal seeks to determine whether phosphorylation of ASCL1 can be induced to inactivate this oncogenic driver in the context of SCLC, a strategy that may reveal an unprecedented, mechanism-based therapy for this treatment resistant disease.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
5F30CA228314-02
Application #
9842268
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Damico, Mark W
Project Start
2018-12-03
Project End
2022-12-02
Budget Start
2019-12-03
Budget End
2020-12-02
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390