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Noncoding RNAs and programmed cell death in hepatocellular carcinoma: Significant role of epigenetic modifications in prognosis, chemoresistance, and tumor recurrence rate.

Authors :
Arefnezhad R
Ashna S
Rezaei-Tazangi F
Arfazadeh SM
Seyedsalehie SS
Yeganeafrouz S
Aghaei M
Sanandaji M
Davoodi R
Abadi SRK
Vosough M
Source :
Cell biology international [Cell Biol Int] 2024 May; Vol. 48 (5), pp. 556-576. Date of Electronic Publication: 2024 Feb 27.
Publication Year :
2024

Abstract

Hepatocellular carcinoma (HCC) is the most common type of liver cancer with a high death rate in the world. The molecular mechanisms related to the pathogenesis of HCC have not been precisely defined so far. Hence, this review aimed to address the potential cross-talk between noncoding RNAs (ncRNAs) and programmed cell death in HCC. All related papers in the English language up to June 2023 were collected and screened. The searched keywords in scientific databases, including Scopus, PubMed, and Google Scholar, were HCC, ncRNAs, Epigenetic, Programmed cell death, Autophagy, Apoptosis, Ferroptosis, Chemoresistance, Tumor recurrence, Prognosis, and Prediction. According to the reports, ncRNAs, comprising long ncRNAs, microRNAs, circular RNAs, and small nucleolar RNAs can affect cell proliferation, migration, invasion, and metastasis, as well as cell death-related processes, such as autophagy, ferroptosis, necroptosis, and apoptosis in HCC by regulating cancer-associated genes and signaling pathways, for example, phosphoinositide 3-kinase/Akt, extracellular signal-regulated kinase/MAPK, and Wnt/β-catenin signaling pathways. It seems that ncRNAs, as epigenetic regulators, can be utilized as biomarkers in diagnosis, prognosis, survival and recurrence rates prediction, chemoresistance, and evaluation of therapeutic response in HCC patients. However, more scientific evidence is suggested to be accomplished to confirm these results.<br /> (© 2024 International Federation for Cell Biology.)

Details

Language :
English
ISSN :
1095-8355
Volume :
48
Issue :
5
Database :
MEDLINE
Journal :
Cell biology international
Publication Type :
Academic Journal
Accession number :
38411312
Full Text :
https://doi.org/10.1002/cbin.12145