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爱泼斯坦-巴尔病毒的潜伏膜蛋白-1抑制鼻咽癌细胞的生长并诱导其对顺铂的敏感性。

Latent membrane protein-1 of Epstein-Barr virus inhibits cell growth and induces sensitivity to cisplatin in nasopharyngeal carcinoma cells.

作者信息

Liu Yu, Wang Xianghong, Lo Angela K F, Wong Yong Chuan, Cheung Annie L M, Tsao Sai Wah

机构信息

Department of Anatomy, Faculty of Medicine, University of Hong Kong, Hong Kong, People's Republic of China.

出版信息

J Med Virol. 2002 Jan;66(1):63-9. doi: 10.1002/jmv.2112.

DOI:10.1002/jmv.2112
PMID:11748660
Abstract

Nasopharyngeal carcinoma is closely associated with Epstein-Barr virus (EBV) and the EBV encoded latent membrane protein-1 expression (LMP1) is commonly found in the tumour cells. LMP1 has been shown to be involved in modulation of cell growth in B cells but the biological properties of LMP1 expression in nasopharyngeal carcinoma cells are less defined. In this study, a full length LMP1 gene was introduced into an EBV negative nasopharyngeal carcinoma cell line, CNE2, and five LMP1-expressing clones were isolated. Expression of LMP1 did not confer cell growth advantage in CNE2 cells; instead, it induced growth inhibition both in vitro and in vivo. In addition, the LMP1 transfected cells were more susceptible to cisplatin-induced cell death and showed 1.4-4.0-fold increased sensitivity to cisplatin compared to the vector infected control clones. The effect of LMP1 on the balance of Bcl-2 and Bax ratio may play a role in inducing susceptibility to cisplatin-induced cell death. These results demonstrated that LMP1 did not confer growth advantage in CNE2 cells, suggesting that expression of LMP1 may not be crucial in sustaining cell growth in established cell lines. Alternatively, LMP1 alone may not be sufficient to facilitate nasopharyngeal carcinoma cell growth and additional oncogenic factors may be needed along with LMP1 in modulating the malignant property of nasopharyngeal carcinoma.

摘要

鼻咽癌与EB病毒(EBV)密切相关,且EBV编码的潜伏膜蛋白1(LMP1)表达常见于肿瘤细胞中。LMP1已被证明参与调节B细胞中的细胞生长,但LMP1在鼻咽癌细胞中的生物学特性尚不清楚。在本研究中,将全长LMP1基因导入EBV阴性鼻咽癌细胞系CNE2,并分离出五个表达LMP1的克隆。LMP1的表达并未赋予CNE2细胞生长优势;相反,它在体外和体内均诱导生长抑制。此外,与载体感染的对照克隆相比,LMP1转染的细胞对顺铂诱导的细胞死亡更敏感,对顺铂的敏感性增加了1.4至4.0倍。LMP1对Bcl-2和Bax比例平衡的影响可能在诱导对顺铂诱导的细胞死亡的易感性中起作用。这些结果表明,LMP1在CNE2细胞中未赋予生长优势,提示LMP1的表达在维持已建立细胞系中的细胞生长方面可能并不关键。或者,单独的LMP1可能不足以促进鼻咽癌细胞生长,在调节鼻咽癌的恶性特性方面可能需要LMP1与其他致癌因素共同作用。

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