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Contribution of Chromosome 9p21‐22 Deletion to the Progression of Human Renal Cell Carcinoma

机译:9p21-22染色体删除对人类肾细胞癌进展的贡献

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摘要

To investigate the possible role of genomic aberrations of chromosome 9p21‐22 in the tumorigenesis of human renal cell carcinoma (RCC), 10 RCC cell lines, 55 primary RCCs and 5 metastatic lesions were studied by Southern blotting and polymerase chain reaction‐based analysis. Nine of 10 RCC cell lines showed a homozygous deletion of MTS1/CDKN2/(p16), while only 1 in 55 primary tumors had this deletion. Loss of heterozygosity on 9p21‐22 was observed in 5 of 10 informative primary RCCs from patients with metastasis, but in only 4 of 31 informative tumors (13%) without metastasis (P= 0.025). Furthermore, 3 of 5 metastatic tumors (60%) showed hemi‐ or homozygous deletion of MTS1/CDKN2. These results indicate that the 9p21‐22 deletion may be a relatively late event in RCC tumorigenesis and could be associated with RCC metastasis.
机译:为了研究9p21-22号染色体的基因组畸变在人类肾细胞癌(RCC)肿瘤发生中的可能作用,通过Southern杂交和基于聚合酶链反应的分析方法研究了10个RCC细胞系,55个原发性RCC和5个转移性病变。 10个RCC细胞系中有9个显示纯合缺失MTS1 / CDKN2 /(p16),而55个原发肿瘤中只有1个具有此缺失。在有转移的患者中,在10例提供信息的原发性RCC中,有5例在9p21-22上观察到杂合性的丧失,但在31例没有转移的信息性肿瘤中,只有4例(13%)发生了Pc = 0.025。此外,在5个转移性肿瘤中,有3个(60%)显示MTS1 / CDKN2半合或纯合缺失。这些结果表明9p21-22缺失可能是RCC肿瘤发生中相对较晚的事件,并且可能与RCC转移有关。

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