Succinate dehydrogenase B-deficient cancer cells are highly sensitive to bromodomain and extra-terminal inhibitors

Satoshi Kitazawa1, Shunsuke Ebara1, Ayumi Ando2

  • 1Oncology Drug Discovery Unit, Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, Fujisawa, Kanagawa, 251-8555, Japan.

Oncotarget
|April 21, 2017
PubMed

Insights

Succinate dehydrogenase B (SDHB) gene mutations drive cancer. SDHB-deficient cells exhibit altered metabolism, relying on glycolysis and glutaminolysis, offering new therapeutic targets like BET inhibitors.

Area of Science:

  • Oncology
  • Cancer Metabolism
  • Molecular Biology

Background:

  • Succinate dehydrogenase B (SDHB) gene mutations are linked to various cancers and poor prognosis.
  • Understanding SDHB-deficient cancer metabolism is crucial for developing targeted therapies.
  • Patient selection based on SDHB mutations can improve clinical trial success rates.

Purpose of the Study:

  • To investigate the metabolic characteristics of SDHB-deficient cancer cells.
  • To identify potential therapeutic vulnerabilities in SDHB-mutant cancers.

Main Methods:

  • Established SDHB knockout colon cancer cell lines using CRISPR/Cas9.
  • Analyzed cellular metabolism via metabolomics and tracer experiments.
  • Assessed cell proliferation using glycolysis and mitochondrial inhibitors.
  • Screened for effective drug compounds, including BET inhibitors.

Main Results:

  • SDHB knockout cells accumulated succinate and decreased fumarate.
  • Reduced oxygen consumption and increased extracellular acidification were observed.
  • Enhanced glycolysis and partial glutaminolysis dependence were confirmed.
  • BET inhibitors targeting c-Myc potently suppressed SDHB knockout cell growth.

Conclusions:

  • SDHB deficiency alters cellular metabolism, promoting glycolysis.
  • SDHB-deficient cancers display specific metabolic vulnerabilities.
  • Targeting these vulnerabilities, such as with BET inhibitors, offers potential new therapeutic strategies.

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