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Targeting the Polycomb repressive complexes in hepatocellular carcinoma: A comprehensive and updated analysis of mechanistic insights and clinical application.

Biochimica et biophysica acta. Reviews on cancer 2026 Vol.1881(3) p. 189589

Liu Z, Wu D, Zhao X, Deng H, Guan X

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Hepatocellular carcinoma (HCC) remains a lethal malignancy with a poor five-year survival rate, leading to a substantial global health burden.

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APA Liu Z, Wu D, et al. (2026). Targeting the Polycomb repressive complexes in hepatocellular carcinoma: A comprehensive and updated analysis of mechanistic insights and clinical application.. Biochimica et biophysica acta. Reviews on cancer, 1881(3), 189589. https://doi.org/10.1016/j.bbcan.2026.189589
MLA Liu Z, et al.. "Targeting the Polycomb repressive complexes in hepatocellular carcinoma: A comprehensive and updated analysis of mechanistic insights and clinical application.." Biochimica et biophysica acta. Reviews on cancer, vol. 1881, no. 3, 2026, pp. 189589.
PMID 41967817

Abstract

Hepatocellular carcinoma (HCC) remains a lethal malignancy with a poor five-year survival rate, leading to a substantial global health burden. Specifically, dysregulated epigenetic modifications cause aberrant gene expression that drives HCC initiation and progression. Among the key epigenetic regulators, the Polycomb repressive complex 1 (PRC1) and 2 (PRC2) mainly mediate gene silencing through histone modifications and exhibit crucial functions in diverse biological processes. A comprehensive understanding of PRC1 and PRC2 roles in HCC is therefore pivotal for developing rational clinical strategies and predictive biomarkers. This review begins by describing several fundamental epigenetic mechanisms and their implications in HCC. Then we emphasize the critical contributions of PRC1 and PRC2 to transcriptional regulation during hepatocarcinogenesis and HCC development. Furthermore, this review discusses the pathological implications of PRC1 or PRC2 dysregulation in key hallmarks of HCC and the related molecular mechanisms. Finally, the therapeutic potential of targeting PRC complexes as novel strategies for cancers, especially for HCC are discussed. In summary, this review synthesizes current knowledge of PRC1 and PRC2 in HCC, underscoring their promise as pivotal targets for guiding the future epigenetic therapies.

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