IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v543y2017i7647d10.1038_nature21408.html
   My bibliography  Save this article

LACTB is a tumour suppressor that modulates lipid metabolism and cell state

Author

Listed:
  • Zuzana Keckesova

    (Whitehead Institute for Biomedical Research)

  • Joana Liu Donaher

    (Whitehead Institute for Biomedical Research)

  • Jasmine De Cock

    (Whitehead Institute for Biomedical Research)

  • Elizaveta Freinkman

    (Whitehead Institute for Biomedical Research
    Metabolon, Inc.)

  • Susanne Lingrell

    (University of Alberta)

  • Daniel A. Bachovchin

    (Broad Institute, Massachusetts Institute of Technology
    Chemical Biology Program, Memorial Sloan Kettering Cancer Center)

  • Brian Bierie

    (Whitehead Institute for Biomedical Research)

  • Verena Tischler

    (Institute of Surgical Pathology, University Hospital Zurich)

  • Aurelia Noske

    (Institute of Surgical Pathology, University Hospital Zurich)

  • Marian C. Okondo

    (Chemical Biology Program, Memorial Sloan Kettering Cancer Center)

  • Ferenc Reinhardt

    (Whitehead Institute for Biomedical Research)

  • Prathapan Thiru

    (Whitehead Institute for Biomedical Research)

  • Todd R. Golub

    (Broad Institute, Massachusetts Institute of Technology)

  • Jean E. Vance

    (University of Alberta)

  • Robert A. Weinberg

    (Whitehead Institute for Biomedical Research
    Massachusetts Institute of Technology
    MIT Ludwig Center for Molecular Oncology, Massachusetts Institute of Technology)

Abstract

Post-mitotic, differentiated cells exhibit a variety of characteristics that contrast with those of actively growing neoplastic cells, such as the expression of cell-cycle inhibitors and differentiation factors. We hypothesized that the gene expression profiles of these differentiated cells could reveal the identities of genes that may function as tumour suppressors. Here we show, using in vitro and in vivo studies in mice and humans, that the mitochondrial protein LACTB potently inhibits the proliferation of breast cancer cells. Its mechanism of action involves alteration of mitochondrial lipid metabolism and differentiation of breast cancer cells. This is achieved, at least in part, through reduction of the levels of mitochondrial phosphatidylserine decarboxylase, which is involved in the synthesis of mitochondrial phosphatidylethanolamine. These observations uncover a novel mitochondrial tumour suppressor and demonstrate a connection between mitochondrial lipid metabolism and the differentiation program of breast cancer cells, thereby revealing a previously undescribed mechanism of tumour suppression.

Suggested Citation

  • Zuzana Keckesova & Joana Liu Donaher & Jasmine De Cock & Elizaveta Freinkman & Susanne Lingrell & Daniel A. Bachovchin & Brian Bierie & Verena Tischler & Aurelia Noske & Marian C. Okondo & Ferenc Rein, 2017. "LACTB is a tumour suppressor that modulates lipid metabolism and cell state," Nature, Nature, vol. 543(7647), pages 681-686, March.
  • Handle: RePEc:nat:nature:v:543:y:2017:i:7647:d:10.1038_nature21408
    DOI: 10.1038/nature21408
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature21408
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/nature21408?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Ipshita Nandi & Linjia Ji & Harvey W. Smith & Daina Avizonis & Vasilios Papavasiliou & Cynthia Lavoie & Alain Pacis & Sherif Attalla & Virginie Sanguin-Gendreau & William J. Muller, 2024. "Targeting fatty acid oxidation enhances response to HER2-targeted therapy," Nature Communications, Nature, vol. 15(1), pages 1-20, December.
    2. Yanying Wang & Jing Wang & Xiaoyu Li & Xushen Xiong & Jianyi Wang & Ziheng Zhou & Xiaoxiao Zhu & Yang Gu & Dan Dominissini & Lei He & Yong Tian & Chengqi Yi & Zusen Fan, 2021. "N1-methyladenosine methylation in tRNA drives liver tumourigenesis by regulating cholesterol metabolism," Nature Communications, Nature, vol. 12(1), pages 1-19, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:543:y:2017:i:7647:d:10.1038_nature21408. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.