Baicalein upregulates DDIT4 expression which mediates mTOR inhibition and growth inhibition in cancer cells

Yujun Wang, Ernest Han, Quanhua Xing, Jin Yan, Amanda Arrington, Charles Wang, Dylan Tully, Claudia M. Kowolik, David M. Lu, Paul H. Frankel, Jing Zhai, Wei Wen, David Horne, M. L.Richard Yip, John H. Yim

Research output: Contribution to journalArticlepeer-review

Abstract

Baicalein is a natural flavone that exhibits anticancer properties. Using microarrays we found that DDIT4 was the highest transcript induced by baicalein in cancer cells. We confirmed in multiple cancer cell lines large, dose-related expression of DDIT4 by quantitative RT-PCR and immunoblot, which correlates with growth inhibition. Time course experiments demonstrate that DDIT4 is rapidly inducible, with high expression maintained for several days in vitro. Induction of DDIT4 expression is p53 independent based on evaluation of p53 knockout cells. Since DDIT4 is known to inhibit mTORC1 activity we confirmed that baicalein suppresses phosphorylation of mTORC1 targets. Using RNA interference we demonstrate that mTORC1 activity and growth inhibition by baicalein is attenuated by knockdown of DDIT4. We furthermore demonstrate suppression of established tumors by baicalein in a mouse model of breast cancer with increased DDIT4 expression in the tumors. Finally, we demonstrate that baicalein upregulates DDIT4 and causes mTORC1 and growth inhibition in platinum resistant cancer cells in marked contrast to platinum chemotherapy treatment. These studies demonstrate that baicalein inhibits mTORC1 through DDIT4 expression, and may be useful in cancer chemotherapy and chemoprevention.

Original languageEnglish (US)
Pages (from-to)170-179
Number of pages10
JournalCancer Letters
Volume358
Issue number2
DOIs
StatePublished - Mar 28 2015

Keywords

  • Baicalein
  • Cellular stress
  • DDIT4
  • IRF1
  • MTOR

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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