IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-42170-0.html
   My bibliography  Save this article

Palmitoylation-driven PHF2 ubiquitination remodels lipid metabolism through the SREBP1c axis in hepatocellular carcinoma

Author

Listed:
  • Do-Won Jeong

    (Seoul National University College of Medicine
    Seoul National University College of Medicine)

  • Jong-Wan Park

    (Seoul National University College of Medicine
    Seoul National University College of Medicine)

  • Kyeong Seog Kim

    (Seoul National University College of Medicine
    Seoul National University College of Medicine and Hospital)

  • Jiyoung Kim

    (Seoul National University College of Medicine)

  • June Huh

    (Korea University)

  • Jieun Seo

    (Seoul National University College of Medicine
    Seoul National University College of Medicine
    Yokohama National University)

  • Ye Lee Kim

    (Seoul National University College of Medicine
    Seoul National University College of Medicine)

  • Joo-Youn Cho

    (Seoul National University College of Medicine
    Seoul National University College of Medicine and Hospital)

  • Kwang-Woong Lee

    (Seoul National University College of Medicine)

  • Junji Fukuda

    (Yokohama National University)

  • Yang-Sook Chun

    (Seoul National University College of Medicine
    Seoul National University College of Medicine
    Seoul National University College of Medicine)

Abstract

Palmitic acid (PA) is the most common fatty acid in humans and mediates palmitoylation through its conversion into palmitoyl coenzyme A. Although palmitoylation affects many proteins, its pathophysiological functions are only partially understood. Here we demonstrate that PA acts as a molecular checkpoint of lipid reprogramming in HepG2 and Hep3B cells. The zinc finger DHHC-type palmitoyltransferase 23 (ZDHHC23) mediates the palmitoylation of plant homeodomain finger protein 2 (PHF2), subsequently enhancing ubiquitin-dependent degradation of PHF2. This study also reveals that PHF2 functions as a tumor suppressor by acting as an E3 ubiquitin ligase of sterol regulatory element-binding protein 1c (SREBP1c), a master transcription factor of lipogenesis. PHF2 directly destabilizes SREBP1c and reduces SREBP1c-dependent lipogenesis. Notably, SREBP1c increases free fatty acids in hepatocellular carcinoma (HCC) cells, and the consequent PA induction triggers the PHF2/SREBP1c axis. Since PA seems central to activating this axis, we suggest that levels of dietary PA should be carefully monitored in patients with HCC.

Suggested Citation

  • Do-Won Jeong & Jong-Wan Park & Kyeong Seog Kim & Jiyoung Kim & June Huh & Jieun Seo & Ye Lee Kim & Joo-Youn Cho & Kwang-Woong Lee & Junji Fukuda & Yang-Sook Chun, 2023. "Palmitoylation-driven PHF2 ubiquitination remodels lipid metabolism through the SREBP1c axis in hepatocellular carcinoma," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42170-0
    DOI: 10.1038/s41467-023-42170-0
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-42170-0
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-42170-0?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
    ---><---

    References listed on IDEAS

    as
    1. Shuyang Chen & Bo Zhu & Chengqian Yin & Wei Liu & Changpeng Han & Baoen Chen & Tongzheng Liu & Xin Li & Xiang Chen & Chunying Li & Limin Hu & Jun Zhou & Zhi-Xiang Xu & Xiumei Gao & Xu Wu & Colin R. Go, 2017. "Palmitoylation-dependent activation of MC1R prevents melanomagenesis," Nature, Nature, vol. 549(7672), pages 399-403, September.
    2. Gloria Pascual & Diana Domínguez & Marc Elosúa-Bayes & Felipe Beckedorff & Carmelo Laudanna & Claudia Bigas & Delphine Douillet & Carolina Greco & Aikaterini Symeonidi & Inmaculada Hernández & Sara Ru, 2021. "Dietary palmitic acid promotes a prometastatic memory via Schwann cells," Nature, Nature, vol. 599(7885), pages 485-490, November.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Mutian Jia & Yuanyuan Wang & Jie Wang & Danhui Qin & Mengge Wang & Li Chai & Yue Fu & Chunyuan Zhao & Chengjiang Gao & Jihui Jia & Wei Zhao, 2023. "Myristic acid as a checkpoint to regulate STING-dependent autophagy and interferon responses by promoting N-myristoylation," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    2. Hai Ni & Yinuo Wang & Kai Yao & Ling Wang & Jiancheng Huang & Yongfang Xiao & Hongyao Chen & Bo Liu & Cliff Y. Yang & Jijun Zhao, 2024. "Cyclical palmitoylation regulates TLR9 signalling and systemic autoimmunity in mice," Nature Communications, Nature, vol. 15(1), pages 1-17, 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:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42170-0. 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.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with 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.