Human endogenous retroviral K element encodes fusogenic activity in melanoma cells

Introduction and Hypothesis: Nuclear atypia with features of multi nuclei have been detected in human melanoma specimens. We found that the K type human endogenous retroviral element (HERV K) is expressed in such cells. Since cellular syncytia can form when cells are infected with retroviruses, we h...

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Main Authors: Gengming Huang, Zhongwu Li, Xiaohua Wan, Yue Wang, Jianli Dong
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2013-01-01
Series:Journal of Carcinogenesis
Subjects:
Online Access:http://www.carcinogenesis.com/article.asp?issn=1477-3163;year=2013;volume=12;issue=1;spage=5;epage=5;aulast=Huang
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spelling doaj-d1ff1c1efc484e5a9a665da1b4f2b9da2020-11-24T22:46:59ZengWolters Kluwer Medknow PublicationsJournal of Carcinogenesis1477-31632013-01-011215510.4103/1477-3163.109032Human endogenous retroviral K element encodes fusogenic activity in melanoma cellsGengming HuangZhongwu LiXiaohua WanYue WangJianli DongIntroduction and Hypothesis: Nuclear atypia with features of multi nuclei have been detected in human melanoma specimens. We found that the K type human endogenous retroviral element (HERV K) is expressed in such cells. Since cellular syncytia can form when cells are infected with retroviruses, we hypothesized that HERV K expressed in melanoma cells may contribute to the formation of multinuclear atypia cells in melanoma. Experiments and Results: We specifically inhibited HERV K expression using RNA interference (RNAi) and monoclonal antibodies and observed dramatic reduction of intercellular fusion of cultured melanoma cells. Importantly, we identified loss of heterozygosity (LOH)of D19S433 in a cell clone that survived and proliferated after cell fusion. Conclusion: Our results support the notion that proteins encoded by HERV K can mediate intercellular fusion of melanoma cells, which may generate multinuclear cells and drive the evolution of genetic changes that provide growth and survival advantages.http://www.carcinogenesis.com/article.asp?issn=1477-3163;year=2013;volume=12;issue=1;spage=5;epage=5;aulast=HuangCell fusionK-type human endogenous retroviral deoxyribonucleic acidmelanoma
collection DOAJ
language English
format Article
sources DOAJ
author Gengming Huang
Zhongwu Li
Xiaohua Wan
Yue Wang
Jianli Dong
spellingShingle Gengming Huang
Zhongwu Li
Xiaohua Wan
Yue Wang
Jianli Dong
Human endogenous retroviral K element encodes fusogenic activity in melanoma cells
Journal of Carcinogenesis
Cell fusion
K-type human endogenous retroviral deoxyribonucleic acid
melanoma
author_facet Gengming Huang
Zhongwu Li
Xiaohua Wan
Yue Wang
Jianli Dong
author_sort Gengming Huang
title Human endogenous retroviral K element encodes fusogenic activity in melanoma cells
title_short Human endogenous retroviral K element encodes fusogenic activity in melanoma cells
title_full Human endogenous retroviral K element encodes fusogenic activity in melanoma cells
title_fullStr Human endogenous retroviral K element encodes fusogenic activity in melanoma cells
title_full_unstemmed Human endogenous retroviral K element encodes fusogenic activity in melanoma cells
title_sort human endogenous retroviral k element encodes fusogenic activity in melanoma cells
publisher Wolters Kluwer Medknow Publications
series Journal of Carcinogenesis
issn 1477-3163
publishDate 2013-01-01
description Introduction and Hypothesis: Nuclear atypia with features of multi nuclei have been detected in human melanoma specimens. We found that the K type human endogenous retroviral element (HERV K) is expressed in such cells. Since cellular syncytia can form when cells are infected with retroviruses, we hypothesized that HERV K expressed in melanoma cells may contribute to the formation of multinuclear atypia cells in melanoma. Experiments and Results: We specifically inhibited HERV K expression using RNA interference (RNAi) and monoclonal antibodies and observed dramatic reduction of intercellular fusion of cultured melanoma cells. Importantly, we identified loss of heterozygosity (LOH)of D19S433 in a cell clone that survived and proliferated after cell fusion. Conclusion: Our results support the notion that proteins encoded by HERV K can mediate intercellular fusion of melanoma cells, which may generate multinuclear cells and drive the evolution of genetic changes that provide growth and survival advantages.
topic Cell fusion
K-type human endogenous retroviral deoxyribonucleic acid
melanoma
url http://www.carcinogenesis.com/article.asp?issn=1477-3163;year=2013;volume=12;issue=1;spage=5;epage=5;aulast=Huang
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