Histone modifications in cervical cancer: Epigenetic mechanisms, functions and clinical implications (Review).

IF 3.9 3区 医学 Q2 ONCOLOGY
Oncology reports Pub Date : 2025-10-01 Epub Date: 2025-08-08 DOI:10.3892/or.2025.8964
Xuewei Li, Min Zhou, Jing Yu, Shaohui Yu, Zheng Ruan
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Abstract

Cervical cancer (CC) poses a substantial global health challenge and it ranks as the fourth most prevalent malignancy among women worldwide. Management strategies include surgical intervention, radiotherapy, chemotherapy and emerging systemic treatments. Although advancements in immunotherapy and targeted therapies have been achieved, the aggressive metastatic nature of the disease, coupled with immune evasion and drug resistance, continues to limit overall survival rates. Therefore, there remains an urgent need to identify novel treatment modalities and more effective therapeutic agents. As fundamental regulators of epigenetic modifications, histone alterations serve a critical role in controlling gene expression, DNA repair mechanisms and cellular differentiation. These modifications include acetylation, methylation, phosphorylation, ubiquitination, ADP‑ribosylation and glycosylation, as well as the more recently identified lactylation and palmitoylation. By restructuring chromatin and facilitating interactions among histones, DNA and regulatory proteins, these modifications exert a substantial influence on cellular functions. Aberrant histone modifications contribute to tumorigenesis, tumor heterogeneity and resistance to conventional anticancer therapies, making them a key focus of oncological research. In recent years, therapeutic strategies targeting histone modifications have gained increasing attention in the treatment of CC. Among these epigenetic alterations, histone acetylation and deacetylation have been extensively studied, with numerous histone deacetylase inhibitors showing promise in preclinical studies. The present review explores the patterns of histone modifications in CC, emphasizing their molecular roles in tumor progression, metastasis and therapeutic resistance. Additionally, histone modification‑driven therapeutic targets are examined, laying the groundwork for future precision medicine approaches in CC treatment.

宫颈癌中的组蛋白修饰:表观遗传机制、功能和临床意义(综述)。
宫颈癌对全球健康构成重大挑战,是全世界妇女中第四大最常见的恶性肿瘤。治疗策略包括手术干预、放疗、化疗和新兴的全身治疗。尽管在免疫治疗和靶向治疗方面取得了进展,但该疾病的侵袭性转移性质,加上免疫逃避和耐药性,继续限制总体生存率。因此,仍然迫切需要确定新的治疗方式和更有效的治疗药物。作为表观遗传修饰的基本调控因子,组蛋白改变在控制基因表达、DNA修复机制和细胞分化中起着至关重要的作用。这些修饰包括乙酰化、甲基化、磷酸化、泛素化、ADP核糖基化和糖基化,以及最近发现的乳酸化和棕榈酰化。通过重组染色质和促进组蛋白、DNA和调控蛋白之间的相互作用,这些修饰对细胞功能产生重大影响。异常组蛋白修饰有助于肿瘤发生、肿瘤异质性和对常规抗癌治疗的耐药性,使其成为肿瘤学研究的重点。近年来,针对组蛋白修饰的治疗策略在CC治疗中受到越来越多的关注。在这些表观遗传改变中,组蛋白乙酰化和去乙酰化已被广泛研究,许多组蛋白去乙酰化酶抑制剂在临床前研究中显示出前景。本文综述了组蛋白修饰在CC中的模式,强调了它们在肿瘤进展、转移和治疗耐药中的分子作用。此外,研究了组蛋白修饰驱动的治疗靶点,为未来CC治疗的精准医学方法奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Oncology reports
Oncology reports 医学-肿瘤学
CiteScore
8.50
自引率
2.40%
发文量
187
审稿时长
3 months
期刊介绍: Oncology Reports is a monthly, peer-reviewed journal devoted to the publication of high quality original studies and reviews concerning a broad and comprehensive view of fundamental and applied research in oncology, focusing on carcinogenesis, metastasis and epidemiology.
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