首页 | 本学科首页   官方微博 | 高级检索  
检索        


Human papillomavirus 16 E6 variants differ in their dysregulation of human keratinocyte differentiation and apoptosis
Authors:Zehbe Ingeborg  Richard Christina  DeCarlo Correne A  Shai Anny  Lambert Paul F  Lichtig Hava  Tommasino Massimo  Sherman Levana
Institution:a Thunder Bay Regional Health Sciences Centre, Regional Cancer Care, Thunder Bay, Ontario, Canada P7B 6V4
b McArdle Laboratory for Cancer Research, University of Wisconsin, Madison, WI, USA
c Department of Human Microbiology, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel
d International Agency for Research on Cancer, World Health Organization, Lyon, France
Abstract:L83V-related variants of human papillomavirus (HPV) 16 E6, exemplified by the Asian-American variant Q14H/H78Y/L83V, were shown to be more prevalent than E6 prototype in progressing lesions and cervical cancer. We evaluated functions relevant to carcinogenesis for the E6 variants L83V, R10/L83V and Q14H/H78Y/L83V as well as the prototype in a model of human normal immortalized keratinocytes (NIKS). All E6 expressing NIKS equally abrogated growth arrest and DNA damage responses. Organotypic cultures derived from these keratinocytes demonstrated hyperplasia and aberrantly expressed keratin 5 in the suprabasal compartment. In contrast, differentiation and induction of apoptosis varied. The E6 variant rafts expressed keratin 10 in nearly all suprabasal cells while the prototype raft showed keratin 10 staining in a subset of suprabasal cells only. In addition, E6 variant NIKS expressing R10G/L83V and Q14H/H78Y/L83V were more prone to undergo cell-detachment-induced apoptosis (anoikis) than NIKS expressing E6 prototype. The combined differentiation and apoptosis pattern of high-risk E6 variants, especially of Q14H/H78Y/L83V, may reflect a phenotype beneficial to carcinogenesis and viral life cycle.
Keywords:Human papillomavirus 16  E6 prototype  E6 variant  Keratinocyte  Proliferation  Differentiation  Apoptosis
本文献已被 ScienceDirect PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号