抗药性
PVT1型
生物
癌症研究
表观遗传学
化疗
生物信息学
长非编码RNA
基因
核糖核酸
遗传学
作者
Saade Abdalkareem Jasim,Ali A. Majeed,Herlina Uinarni,Mohammed S. Alshuhri,Abdullah Alzahrani,Abeer A. Ibrahim,Ahmed Alawadi,Noor K. Abed Al-Abadi,Yasser Fakri Mustafa,Batool Ali Ahmed
标识
DOI:10.1016/j.prp.2024.155119
摘要
According to estimates, cancer will be the leading cause of death globally in 2022, accounting for 9.6 million deaths. At present, the three main therapeutic modalities utilized to treat cancer are radiation therapy, chemotherapy, and surgery. However, during treatment, tumor cells resistant to chemotherapy may arise. Drug resistance remains a major oppose since it often leads to therapeutic failure. Furthermore, the term "acquired drug resistance" describes the situation where tumor cells already display drug resistance before undergoing chemotherapy. However, little is still known about the basic mechanisms underlying chemotherapy-induced drug resistance. The development of new technologies and bioinformatics has led to the discovery of additional genes associated with drug resistance. Long noncoding RNA plasmacytoma variant translocation 1 (PVT1) has been linked to an increased risk of cancer, according to a growing body of research. Apart from biological functions associated with cell division, development, pluripotency, and cell cycle, lncRNA PVT1 contributes significantly to the regulation of various aspects of genome function, such as transcription, splicing, and epigenetics. The article will address the mechanism by which lncRNA PVT1 influences drug resistance in cancer cells.
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