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日本語AIでPubMedを検索

日本語AIでPubMedを検索

PubMedの提供する医学論文データベースを日本語で検索できます。AI(Deep Learning)を活用した機械翻訳エンジンにより、精度高く日本語へ翻訳された論文をご参照いただけます。
J. Pathol..2020 Apr;doi: 10.1002/path.5451.Epub 2020-04-18.

FDXRはIRP2を介してTP73腫瘍抑制因子を制御し、老化と腫瘍抑制を調節する

FDXR regulates TP73 tumor suppressor via IRP2 to modulate aging and tumor suppression.

  • Jin Zhang
  • Xiangmudong Kong
  • Yanhong Zhang
  • Wenqiang Sun
  • Jian Wang
  • Mingyi Chen
  • Xinbin Chen
PMID: 32304229 DOI: 10.1002/path.5451.

抄録

Ferredoxin reductase (FDXR) is a mitochondrial flavoprotein that initiates electron transport from NADPH to several cytochromes P450 via two electron carriers, ferredoxin 1 (FDX1) and FDX2. FDXR is the sole ferredoxin reductase in humans and plays a critical role in steroidogenesis and biosynthesis of heme and iron-sulfur clusters. However, much less is known about the role of FDXR in cancer. Here, we show that FDXR plays a role in tumorigenesis by modulating expression of the tumor suppressor p73. By using genetically modified mouse models, we recently showed that mice deficient in either Fdxr or Trp73 had a shorter lifespan and were prone to spontaneous tumors as compared with wild-type (WT) mice. Interestingly, compound Trp73 ;Fdxr mice lived longer and developed fewer tumors when compared with Fdxr or Trp73 mice. Moreover, we found that cellular senescence was increased in Trp73 and Fdxr mouse embryonic fibroblasts (MEFs), which was further increased in Trp73 ;Fdxr MEFs, as compared with that in WT MEFs. As FDXR is regulated by p73, we examined whether there was a feedback regulation between p73 and FDXR. Indeed, we found that Trp73 expression was decreased by loss of Fdxr in MEFs and that FDXR is required for p73 expression in multiple human cancer cell lines independent of p53. Mechanistically, we found that loss of FDXR, via FDX2, increased expression of iron-binding protein 2 (IRP2), which subsequently repressed TP73 mRNA stability. We also showed that TP73 transcript contained an iron response element in its 3'UTR, which was required for IRP2 to destabilize TP73 mRNA. Together, these data reveal a novel regulation of p73 by FDXR via IRP2 and that the FDXR-p73 axis plays a critical role in aging and tumor suppression. © 2020 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

© 2020 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.