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2000
Volume 11, Issue 3
  • ISSN: 1574-8928
  • E-ISSN: 2212-3970

Abstract

Recent studies show that enhanced mitochondrial biogenesis can “fuel” the cancer cells to grow and migrate. It is therefore proposed that inhibiting the mitochondrial biogenesis could be a new approach to cancer therapy. This review summarizes recent patents and papers in the development of small molecule inhibitors of key regulators responsible for tumor mitochondrial biogenesis, including PPARγcoactivator-1α(PGC-1α), PPARγcoactivator-1β, estrogen-related receptor family (ERRs), estrogen receptor α(ERα), mammalian target of rapamycin, c-Myc and PPARs.

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/content/journals/pra/10.2174/1574892811666160418123628
2016-08-01
2025-09-28
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/content/journals/pra/10.2174/1574892811666160418123628
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  • Article Type:
    Research Article
Keyword(s): Cancer; energy metabolism; inhibitors; mitochondrial biogenesis; PGC-1α; tumor migration
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