{"title":"PROX1: a key regulator of hepatocyte identity and tumorigenesis","authors":"Terence Kin Wah. Lee, Stephanie Ma","doi":"10.1158/0008-5472.can-25-1377","DOIUrl":null,"url":null,"abstract":"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 pathological 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 of cancer development. A recent research article published in Nature Genetics unveiled the identification of a liver-specific protein, named PROX1, which maintains cellular identity and impedes the initiation and advancement of liver cancer. Analysis of liver cancer patient specimens 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.","PeriodicalId":9441,"journal":{"name":"Cancer research","volume":"33 1","pages":""},"PeriodicalIF":12.5000,"publicationDate":"2025-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1158/0008-5472.can-25-1377","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
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 pathological 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 of cancer development. A recent research article published in Nature Genetics unveiled the identification of a liver-specific protein, named PROX1, which maintains cellular identity and impedes the initiation and advancement of liver cancer. Analysis of liver cancer patient specimens 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.
期刊介绍:
Cancer Research, published by the American Association for Cancer Research (AACR), is a journal that focuses on impactful original studies, reviews, and opinion pieces relevant to the broad cancer research community. Manuscripts that present conceptual or technological advances leading to insights into cancer biology are particularly sought after. The journal also places emphasis on convergence science, which involves bridging multiple distinct areas of cancer research.
With primary subsections including Cancer Biology, Cancer Immunology, Cancer Metabolism and Molecular Mechanisms, Translational Cancer Biology, Cancer Landscapes, and Convergence Science, Cancer Research has a comprehensive scope. It is published twice a month and has one volume per year, with a print ISSN of 0008-5472 and an online ISSN of 1538-7445.
Cancer Research is abstracted and/or indexed in various databases and platforms, including BIOSIS Previews (R) Database, MEDLINE, Current Contents/Life Sciences, Current Contents/Clinical Medicine, Science Citation Index, Scopus, and Web of Science.