During ontogeny, the modulation of cell fate plasticity in stem cells is meticulously controlled as they undergo differentiation into distinct cell lineages. Dysregulation of this plasticity can result in pathologic conditions, such as oncogenesis. Transcription factors are pivotal in orchestrating this cellular transition by initiating gene expression programs that define cell identity. Notably, the investigation of transcriptional repressors has garnered significant attention in elucidating the susceptibility to cancer development. A recent research article published in Nature Genetics unveiled the identification of a liver-specific protein named prospero homeobox protein 1 (PROX1), which maintains cellular identity and impedes the initiation and advancement of liver cancer. Analysis of specimens from patients with liver cancer demonstrated a positive association between elevated levels of PROX1 and improved prognosis, as well as extended survival. Utilizing various liver cancer mouse models, the researchers demonstrated that PROX1 can impede tumor initiation and decelerate cancer progression. This study offers valuable insights for potential therapeutic interventions and introduces novel opportunities for investigating “safeguard repressors” in diverse tissue types.
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1 June 2025
In the Spotlight|
June 02 2025
PROX1: A Key Regulator of Hepatocyte Identity and Tumorigenesis Available to Purchase
Terence Kin Wah Lee
;
Terence Kin Wah Lee
*
1Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, Hong Kong SAR, China.
*Corresponding Authors: Stephanie Ma, School of Biomedical Sciences, The University of Hong Kong, L1-47, Laboratory Block, Hong Kong, Hong Kong SAR, China. E-mail: [email protected]; and Terence Kin Wah Lee, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Room 805, Block Y, Lee Shau Kee Building, Hong Kong, Hong Kong SAR, China. E-mail: [email protected]
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Stephanie Ma
Stephanie Ma
*
2School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
3State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, Hong Kong SAR, China.
*Corresponding Authors: Stephanie Ma, School of Biomedical Sciences, The University of Hong Kong, L1-47, Laboratory Block, Hong Kong, Hong Kong SAR, China. E-mail: [email protected]; and Terence Kin Wah Lee, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Room 805, Block Y, Lee Shau Kee Building, Hong Kong, Hong Kong SAR, China. E-mail: [email protected]
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*Corresponding Authors: Stephanie Ma, School of Biomedical Sciences, The University of Hong Kong, L1-47, Laboratory Block, Hong Kong, Hong Kong SAR, China. E-mail: [email protected]; and Terence Kin Wah Lee, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Room 805, Block Y, Lee Shau Kee Building, Hong Kong, Hong Kong SAR, China. E-mail: [email protected]
Cancer Res 2025;85:1957–9
Received:
March 26 2025
Accepted:
March 27 2025
Online ISSN: 1538-7445
Print ISSN: 0008-5472
©2025 American Association for Cancer Research
2025
American Association for Cancer Research
Cancer Res (2025) 85 (11): 1957–1959.
Article history
Received:
March 26 2025
Accepted:
March 27 2025
Citation
Terence Kin Wah Lee, Stephanie Ma; PROX1: A Key Regulator of Hepatocyte Identity and Tumorigenesis. Cancer Res 1 June 2025; 85 (11): 1957–1959. https://doi.org/10.1158/0008-5472.CAN-25-1377
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