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对人类肿瘤和人类恶性细胞系进行BK病毒特异性DNA序列分析。

Analysis of human tumors and human malignant cell lines for BK virus-specific DNA sequences.

作者信息

Wold W S, Mackey J K, Brackmann K H, Takemori N, Rigden P, Green M

出版信息

Proc Natl Acad Sci U S A. 1978 Jan;75(1):454-8. doi: 10.1073/pnas.75.1.454.

Abstract

Most humans in the United States have been infected with BK virus (BKV), a human papovavirus. Because BKV has oncogenic properties, we have investigated whether it may be a cause of human cancer. Basic principles of tumor virology imply that BKV-induced tumors should contain BKV DNA sequences. Therefore, we assayed (by molecular hybridization) DNA from human tumors and malignant cell lines for BKV DNA, using BKV [(32)P]DNA as probe. The BKV [(32)P]DNA was labeled in vitro (nick translation) to specific activities of 1 to 2 x 10(8) cpm/mug. The BKV DNA used to prepare our probes had the properties expected of authentic BKV genomes, including density of superhelical DNA, sedimentation velocity in alkaline and neutral sucrose gradients, production of one fragment by endonuclease EcoRI cleavage and four fragments by endonuclease Hin II + III cleavage and reassociation properties. From these studies we conclude that our BKV probes hybridized well, and represented bona fide BKV DNA. Using three different BKV [(32)P]DNA probes, i.e., from three distinct plaque isolates, we have analyzed DNA from BKV-transformed cells, normal human tissues, and a large number of human tumors. All human DNAs (cell lines, normal tissues, tumors) hybridized 5% with BKV DNA. Hybridization analysis of BKV-transformed hamster cell DNA indicated 5-6 copies of at least 88% of the BKV genome per cell. No BKV DNA sequences were detected (above the normal 5% hybridization to all human DNAs) in the following normal human tissues: 10 kidney (BKV is usually isolated from urine), 3 spleen, 13 lung, 23 colon, 2 rectum, 1 ileum, and 1 skin. No BKV-specific DNA was found in 166 tumors, including 5 carcinomas (Ca) of stomach, 3 Ca small intestine, 26 Ca colon, 9 Ca rectum, 31 Ca lung, 9 adenocarcinomas and 5 oat cell carcinomas of lung, 17 melanomas, 5 Ca prostate, 4 Ca bladder, 6 Wilms tumors, 4 hypernephromas, 15 Ca kidney, 7 brain tumors, 5 Hodgkin lymphomas, 10 lymphomas (immunosuppressed patients have a high incidence of lymphomas), 2 reticulum cell sarcomas (spleen), and 3 skin tumors. We have also analyzed 7 human malignant cell lines (melanoma, lung, rhabdomyosarcoma, and glioblastomas), including several clones of a lung melanoma line; no BKV DNA sequences were detected. Because our probes could detect one copy of BKV DNA if only 10% of the cells were tumor cells, our results are very strong evidence that the tumors we analyzed did not have a BKV etiology. The tumors we tested represent about 50% of all cancers in the United States; there is no evidence that BKV is involved in the etiology of these types of tumors.

摘要

美国大多数人都感染过BK病毒(BKV),一种人乳头瘤多瘤空泡病毒。由于BKV具有致癌特性,我们研究了它是否可能是人类癌症的病因。肿瘤病毒学的基本原理表明,BKV诱导的肿瘤应含有BKV DNA序列。因此,我们以BKV [(32)P] DNA为探针,通过分子杂交检测了人类肿瘤和恶性细胞系中的DNA,以寻找BKV DNA。BKV [(32)P] DNA在体外通过切口平移法标记,比活度为1至2×10(8)cpm/μg。用于制备我们探针的BKV DNA具有正宗BKV基因组预期的特性,包括超螺旋DNA的密度、在碱性和中性蔗糖梯度中的沉降速度、经核酸内切酶EcoRI切割产生一个片段以及经核酸内切酶Hin II + III切割产生四个片段以及复性特性。从这些研究中我们得出结论,我们的BKV探针杂交良好,代表了真正的BKV DNA。使用三种不同的BKV [(32)P] DNA探针,即来自三个不同噬菌斑分离株的探针,我们分析了BKV转化细胞、正常人体组织和大量人类肿瘤的DNA。所有人类DNA(细胞系、正常组织、肿瘤)与BKV DNA的杂交率均为5%。对BKV转化的仓鼠细胞DNA的杂交分析表明,每个细胞至少有88%的BKV基因组的5至6个拷贝。在以下正常人体组织中未检测到BKV DNA序列(高于与所有人类DNA的正常5%杂交率):10个肾脏(BKV通常从尿液中分离出来)、3个脾脏、13个肺、23个结肠、2个直肠、1个回肠和1个皮肤。在166个肿瘤中未发现BKV特异性DNA,包括5例胃癌、3例小肠癌、26例结肠癌、9例直肠癌、31例肺癌、9例肺腺癌和5例肺燕麦细胞癌、17例黑色素瘤、5例前列腺癌、4例膀胱癌、6例肾母细胞瘤、4例肾上腺皮质癌、15例肾癌、7例脑肿瘤、5例霍奇金淋巴瘤、10例淋巴瘤(免疫抑制患者淋巴瘤发病率高)、2例网状细胞肉瘤(脾脏)和3例皮肤肿瘤。我们还分析了7个人类恶性细胞系(黑色素瘤、肺癌、横纹肌肉瘤和成胶质细胞瘤),包括一个肺黑色素瘤系的几个克隆;未检测到BKV DNA序列。由于我们的探针如果只有10%的细胞是肿瘤细胞就能检测到一个拷贝的BKV DNA,我们的结果是非常有力的证据,表明我们分析的肿瘤没有BKV病因。我们测试的肿瘤约占美国所有癌症的50%;没有证据表明BKV参与这些类型肿瘤的病因。

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