Bowcock A M, Pinto M R, Bey E, Kuyl J M, Dusheiko G M, Bernstein R
Cancer Genet Cytogenet. 1985 Sep;18(1):19-26. doi: 10.1016/0165-4608(85)90034-2.
The chromosomal sites at which hepatitis B virus (HBV) DNA is integrated into the genome of the hepatocellular carcinoma (HCC) cell line, PLC/PRF/5 were investigated in an attempt to understand the mechanisms by which hepatitis B virus may induce malignant transformation. In situ hybridization of an HBV DNA probe to metaphase chromosomes of the PLC/PRF/5 cell line, followed by statistical analysis, identified three integration sites; these were 15q22-q23, 11q22, and 18q12. In particular, hybridization to chromosome #15, which is present in four copies in complete metaphases of this cell line, was highly significant (p much less than 0.0005).
为了了解乙型肝炎病毒(HBV)可能诱导恶性转化的机制,对乙型肝炎病毒DNA整合到肝癌(HCC)细胞系PLC/PRF/5基因组中的染色体位点进行了研究。用HBV DNA探针与PLC/PRF/5细胞系的中期染色体进行原位杂交,随后进行统计分析,确定了三个整合位点;分别为15q22-q23、11q22和18q12。特别是,与该细胞系完整中期相中四个拷贝的第15号染色体的杂交具有高度显著性(p远小于0.0005)。