The transmembrane channel-like protein family and human papillomaviruses Insights into epidermodysplasia verruciformis and progression to squamous cell carcinoma

被引:9
作者
Horton, Jaime S. [1 ,2 ]
Stokes, Alexander J. [1 ,2 ,3 ]
机构
[1] Univ Hawaii, John A Burns Sch Med, Expt Med Lab, Honolulu, HI 96822 USA
[2] Univ Hawaii, John A Burns Sch Med, Dept Cell & Mol Biol, Honolulu, HI 96822 USA
[3] Chaminade Univ, Honolulu, HI USA
来源
ONCOIMMUNOLOGY | 2014年 / 3卷 / 04期
基金
美国国家卫生研究院;
关键词
Epidermodysplasia verruciformis; TMC8; TMC6; EVER1; EVER2; papillomavirus; cutaneous squamous cell carcinoma; TMC GENE FAMILY; MEDIATED-IMMUNITY; SKIN-CANCER; PRIMARY IMMUNODEFICIENCY; SUSCEPTIBILITY LOCUS; E6/E7; EXPRESSION; CERVICAL-CANCER; HEARING-LOSS; E6; PROTEINS; HIGH-RISK;
D O I
10.4161/onci.28288
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epidermodysplasia verruciformis (EV) is a rare genodermatosis characterized by increased sensitivity to infection by the beta-subtype of human papillomaviruses (beta-HPVs), causing persistent, tinea versicolor-like dermal lesions. In a majority of affected individuals, these macular lesions progress to invasive cutaneous squamous cell carcinoma (CSCC) in sun-exposed areas. While mutations in transmembrane channel-like 6 (TMC6/EVER1) and 8 (TMC8/EVER2) have been causally linked to EV, their molecular functions are unclear. It is likely that their protective effects involve regulation of the beta-HPV life cycle, host keratinocyte apoptosis vs. survival balance and/or T-cell interaction with infected host cells.
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页数:11
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