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用爱泼斯坦-巴尔病毒对鼻咽癌细胞进行重复感染。

Superinfection epithelial nasopharyngeal carcinoma cells with Epstein-Barr virus.

作者信息

Glaser R, de Thé G, Lenoir G, Ho J H

出版信息

Proc Natl Acad Sci U S A. 1976 Mar;73(3):960-3. doi: 10.1073/pnas.73.3.960.

DOI:10.1073/pnas.73.3.960
PMID:176664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC336040/
Abstract

Attempts were made to superinfect epithelial explant cell cultures prepared from nasopharyngeal carcinomas with Epstein-Barr virus. Virus-specific markers were observed in such cultures 3 days after superinfection. In addition, expression of Epstein-Barr virus early antigens was observed in epithelial cell explant cultures treated with iododeoxyuridine. The results suggest that epithelial cells of at least certain nasopharyngeal carcinomas possess the receptor for the Epstein-Barr virus and that the latent virus genome can be induced from epithelial cells prepared from such tumors.

摘要

尝试用爱泼斯坦-巴尔病毒对从鼻咽癌制备的上皮外植体细胞培养物进行再次感染。再次感染3天后,在这种培养物中观察到病毒特异性标志物。此外,在用碘脱氧尿苷处理的上皮细胞外植体培养物中观察到爱泼斯坦-巴尔病毒早期抗原的表达。结果表明,至少某些鼻咽癌的上皮细胞具有爱泼斯坦-巴尔病毒的受体,并且可以从由此类肿瘤制备的上皮细胞中诱导出潜伏的病毒基因组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53f/336040/b2ef633c2b8f/pnas00672-0304-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53f/336040/6e55ab61a14b/pnas00672-0303-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53f/336040/cf7a624e9840/pnas00672-0303-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53f/336040/b2ef633c2b8f/pnas00672-0304-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53f/336040/6e55ab61a14b/pnas00672-0303-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53f/336040/cf7a624e9840/pnas00672-0303-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c53f/336040/b2ef633c2b8f/pnas00672-0304-a.jpg

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1
Superinfection epithelial nasopharyngeal carcinoma cells with Epstein-Barr virus.用爱泼斯坦-巴尔病毒对鼻咽癌细胞进行重复感染。
Proc Natl Acad Sci U S A. 1976 Mar;73(3):960-3. doi: 10.1073/pnas.73.3.960.
2
Presence of Epstein-Barr virus nuclear antigen in nasopharyngeal carcinoma biopsies and their derived cultures.
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IARC Sci Publ (1971). 1978(20):333-45.
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Int J Cancer. 1974 Nov 15;14(5):580-8. doi: 10.1002/ijc.2910140504.

引用本文的文献

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Epstein-Barr virus infection of human gastric carcinoma cells: implication of the existence of a new virus receptor different from CD21.爱泼斯坦-巴尔病毒对人胃癌细胞的感染:存在不同于CD21的新型病毒受体的意义。
J Virol. 1997 Jul;71(7):5688-91. doi: 10.1128/JVI.71.7.5688-5691.1997.
2
The mechanism of Epstein-Barr virus infection in nasopharyngeal carcinoma cells.爱泼斯坦-巴尔病毒感染鼻咽癌细胞的机制。
Am J Pathol. 1997 May;150(5):1745-56.
3
Epstein-Barr virus transcription in nasopharyngeal carcinoma.鼻咽癌中的爱泼斯坦-巴尔病毒转录

本文引用的文献

1
Antibodies to Epstein-Barr virus in nasopharyngeal carcinoma, other head and neck neoplasms, and control groups.鼻咽癌、其他头颈部肿瘤及对照组中针对EB病毒的抗体。
J Natl Cancer Inst. 1970 Jan;44(1):225-31.
2
Epstein-Barr virus-associated antibody patterns in carcinoma of the post-nasal space.鼻后间隙癌中与爱泼斯坦-巴尔病毒相关的抗体模式
Clin Exp Immunol. 1969 Nov;5(5):443-59.
3
Nasopharyngeal carcinoma. 3. Ultrastructure of different growths leading to lymphoblastoid transformation in vitro.鼻咽癌。3. 体外导致淋巴母细胞样转化的不同生长的超微结构
J Virol. 1983 Dec;48(3):580-90. doi: 10.1128/JVI.48.3.580-590.1983.
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Sendai virus envelopes can mediate Epstein-Barr virus binding to and penetration into Epstein-Barr virus receptor-negative cells.仙台病毒包膜可介导爱泼斯坦-巴尔病毒与爱泼斯坦-巴尔病毒受体阴性细胞结合并侵入该细胞。
J Virol. 1983 Apr;46(1):325-32. doi: 10.1128/JVI.46.1.325-332.1983.
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Epstein-Barr virus-lymphoid cell interactions. III. Effect of concanavalin A and saccharides on Epstein-Barr virus penetration.爱泼斯坦-巴尔病毒与淋巴细胞的相互作用。III. 伴刀豆球蛋白A和糖类对爱泼斯坦-巴尔病毒穿透的影响。
J Virol. 1982 May;42(2):402-10. doi: 10.1128/JVI.42.2.402-410.1982.
6
Induction of Epstein-Barr virus nuclear antigen and DNA synthesis in a human epithelial cell line after Epstein-Barr virus infection.爱泼斯坦-巴尔病毒感染后人类上皮细胞系中爱泼斯坦-巴尔病毒核抗原的诱导及DNA合成
J Virol. 1982 Feb;41(2):703-8. doi: 10.1128/JVI.41.2.703-708.1982.
7
Expression of Epstein-Barr viral early antigen in monolayer tissue cultures after transfection with viral DNA and DNA fragments.用病毒DNA和DNA片段转染后,单层组织培养物中EB病毒早期抗原的表达。
J Virol. 1981 Dec;40(3):861-9. doi: 10.1128/JVI.40.3.861-869.1981.
8
An Epstein--Barr virus early protein induces cell fusion.一种爱泼斯坦-巴尔病毒早期蛋白可诱导细胞融合。
Proc Natl Acad Sci U S A. 1981 Nov;78(11):7162-5. doi: 10.1073/pnas.78.11.7162.
9
Pleiotropic expression of Epstein--Barr virus DNA in human epithelial cells.爱泼斯坦-巴尔病毒DNA在人上皮细胞中的多效性表达
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5852-5. doi: 10.1073/pnas.78.9.5852.
10
Two epithelial tumor cell lines (HNE-1 and HONE-1) latently infected with Epstein-Barr virus that were derived from nasopharyngeal carcinomas.两种来自鼻咽癌的、潜伏感染了爱泼斯坦-巴尔病毒的上皮肿瘤细胞系(HNE-1和HONE-1)。
Proc Natl Acad Sci U S A. 1989 Dec;86(23):9524-8. doi: 10.1073/pnas.86.23.9524.
J Natl Cancer Inst. 1973 Jul;51(1):67-80. doi: 10.1093/jnci/51.1.67.
4
Nasopharyngeal carcinoma. II. Ultrastructure of normal mucosa, tumor biopsies, and subsequent epithelial growth in vitro.鼻咽癌。II. 正常黏膜、肿瘤活检组织及后续体外上皮生长的超微结构
J Natl Cancer Inst. 1972 Jan;48(1):73-86.
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Nasopharyngeal carcinoma. IV. Evolution of complement-fixing antibodies during the course of the disease.鼻咽癌。IV. 疾病过程中补体结合抗体的演变。
Int J Cancer. 1973 Sep 15;12(2):368-77. doi: 10.1002/ijc.2910120208.
6
Observations on the resistance of Fpstein-Barr virus DNA synthesis to hydroxyurea.关于爱泼斯坦 - 巴尔病毒DNA合成对羟基脲抗性的观察
Virology. 1974 Nov;62(1):102-11. doi: 10.1016/0042-6822(74)90306-7.
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B-cell characteristics of human peripheral and cord blood lymphocytes transformed by Epstein-Barr virus.由爱泼斯坦-巴尔病毒转化的人外周血和脐带血淋巴细胞的B细胞特征
J Natl Cancer Inst. 1974 Apr;52(4):1081-6. doi: 10.1093/jnci/52.4.1081.
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Nasopharyngeal carcinoma (NPC). VI. Presence of an EBV nuclear antigen in fresh tumour biopsies. Preliminary results.鼻咽癌(NPC)。六、新鲜肿瘤活检中EB病毒核抗原的存在。初步结果。
Biomedicine. 1973 Aug 10;19(8):349-52.
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Antibodies to Epstein-Barr virus-related antigens in nasopharyngeal carcinoma. Comparison of active cases with long-term survivors.鼻咽癌中与 Epstein-Barr 病毒相关抗原的抗体。活动期病例与长期存活者的比较。
J Natl Cancer Inst. 1973 Aug;51(2):361-9.
10
Synthesis of Epstein-Barr virus antigens and DNA in activated Burkitt somatic cell hybrids.爱泼斯坦-巴尔病毒抗原及DNA在活化的伯基特体细胞杂种中的合成
Virology. 1973 Sep;55(1):62-9. doi: 10.1016/s0042-6822(73)81008-6.