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UCHL1 provides diagnostic and antimetastatic strategies due to its deubiquitinating effect on HIF-1α

Author

Listed:
  • Yoko Goto

    (Kyoto University Graduate School of Medicine
    Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University)

  • Lihua Zeng

    (Kyoto University Graduate School of Medicine
    Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University
    Fourth Military Medical University)

  • Chan Joo Yeom

    (Kyoto University Graduate School of Medicine
    Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University)

  • Yuxi Zhu

    (Kyoto University Graduate School of Medicine
    Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University
    First Affiliated Hospital of Chongqing Medical University)

  • Akiyo Morinibu

    (Kyoto University Graduate School of Medicine
    Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University)

  • Kazumi Shinomiya

    (Kyoto University Graduate School of Medicine
    Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University)

  • Minoru Kobayashi

    (Kyoto University Graduate School of Medicine
    Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University)

  • Kiichi Hirota

    (Kyoto University Hospital, Kyoto University)

  • Satoshi Itasaka

    (Kyoto University Graduate School of Medicine)

  • Michio Yoshimura

    (Kyoto University Graduate School of Medicine)

  • Keiji Tanimoto

    (Research Institute for Radiation Biology and Medicine, Hiroshima University)

  • Masae Torii

    (Kyoto University Graduate School of Medicine)

  • Terumasa Sowa

    (Kyoto University Graduate School of Medicine)

  • Toshi Menju

    (Kyoto University Graduate School of Medicine)

  • Makoto Sonobe

    (Kyoto University Graduate School of Medicine)

  • Hideaki Kakeya

    (Graduate School of Pharmaceutical Sciences, Kyoto University)

  • Masakazu Toi

    (Kyoto University Graduate School of Medicine)

  • Hiroshi Date

    (Kyoto University Graduate School of Medicine)

  • Ester M. Hammond

    (CRUK/MRC Oxford Institute for Radiation Oncology, University of Oxford)

  • Masahiro Hiraoka

    (Kyoto University Graduate School of Medicine)

  • Hiroshi Harada

    (Kyoto University Graduate School of Medicine
    Group of Radiation and Tumor Biology, Career-Path Promotion Unit for Young Life Scientists, Kyoto University
    Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST))

Abstract

Hypoxia-inducible factor 1 (HIF-1) plays a role in tumour metastases; however, the genes that activate HIF-1 and subsequently promote metastases have yet to be identified. Here we show that Ubiquitin C-terminal hydrolase-L1 (UCHL1) abrogates the von Hippel–Lindau-mediated ubiquitination of HIF-1α, the regulatory subunit of HIF-1, and consequently promotes metastasis. The aberrant overexpression of UCHL1 facilitates distant tumour metastases in a HIF-1-dependent manner in murine models of pulmonary metastasis. Meanwhile, blockade of the UCHL1–HIF-1 axis suppresses the formation of metastatic tumours. The expression levels of UCHL1 correlate with those of HIF-1α and are strongly associated with the poor prognosis of breast and lung cancer patients. These results indicate that UCHL1 promotes metastases as a deubiquitinating enzyme for HIF-1α, which justifies exploiting it as a prognostic marker and therapeutic target of cancers.

Suggested Citation

  • Yoko Goto & Lihua Zeng & Chan Joo Yeom & Yuxi Zhu & Akiyo Morinibu & Kazumi Shinomiya & Minoru Kobayashi & Kiichi Hirota & Satoshi Itasaka & Michio Yoshimura & Keiji Tanimoto & Masae Torii & Terumasa , 2015. "UCHL1 provides diagnostic and antimetastatic strategies due to its deubiquitinating effect on HIF-1α," Nature Communications, Nature, vol. 6(1), pages 1-13, May.
  • Handle: RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7153
    DOI: 10.1038/ncomms7153
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    Cited by:

    1. Christian Grethe & Mirko Schmidt & Gian-Marvin Kipka & Rachel O’Dea & Kai Gallant & Petra Janning & Malte Gersch, 2022. "Structural basis for specific inhibition of the deubiquitinase UCHL1," Nature Communications, Nature, vol. 13(1), pages 1-17, December.

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