Fan Chun-Yang
Department of Pathology and Otolaryngology, University of Arkansas for Medical Sciences and Central Arkansas Veterans Healthcare System, 4300 West 7th Street (113/LR), Little Rock, AR 72205, USA.
Curr Oncol Rep. 2004 Mar;6(2):152-61. doi: 10.1007/s11912-004-0027-0.
Head and neck cancers are a group of malignancies with diverse biologic behaviors and a strong, well-established association with tobacco and alcohol use. Although the hunt for genetic alterations in head and neck cancer has continued in the past two decades, with unequivocal proof of a genetic role in multistage head and neck carcinogenesis, epigenetic alteration in association with promoter CpG island hypermethylation has emerged in the past few years as one of the most active areas of cancer research. It is now firmly believed that, in cancer cells, promoter CpG island hypermethylation (epigenetic alteration) represents a bona fide alternative mechanism, as opposed to genetic factors, such as gene mutations and deletion, in the inactivation of many tumor-suppressor genes. It is also realized that epigenetic and genetic factors often work together, affecting multiple cellular pathways, such as cell-cycle regulation, DNA repair, apoptosis, angiogenesis, and cell-to-cell adhesion, during the process of tumor growth and progression.
头颈癌是一组具有不同生物学行为的恶性肿瘤,与烟草和酒精使用有着密切且已明确的关联。尽管在过去二十年中一直在对头颈癌的基因改变进行研究,并且已经明确证明基因在头颈癌多阶段致癌过程中发挥作用,但在过去几年中,与启动子CpG岛高甲基化相关的表观遗传改变已成为癌症研究最活跃的领域之一。现在人们坚信,在癌细胞中,启动子CpG岛高甲基化(表观遗传改变)代表了一种真正的替代机制,与基因突变和缺失等遗传因素相反,它导致许多肿瘤抑制基因失活。人们还认识到,表观遗传和遗传因素常常共同作用,在肿瘤生长和进展过程中影响多个细胞途径,如细胞周期调控、DNA修复、细胞凋亡、血管生成和细胞间黏附。