Nagao Kazuhiro, Yamaguchi Shiro, Matsuyama Hideyasu, Korenaga Yoshihito, Hirata Hiroshi, Yoshihiro Satoru, Fukunaga Koji, Oba Kazuo, Naito Katsusuke
Department of Urology, Yamaguchi University School of Medicine, 1-1-1 Minami-Kogushi, Ube, Yamaguchi 755-8505, Japan.
Cancer Genet Cytogenet. 2005 Jul 1;160(1):43-8. doi: 10.1016/j.cancergencyto.2004.11.015.
Little is known about the clinical significance at the frequent association of 3p loss with 5q gain/loss in conventional renal cell carcinoma (RCC). We analyzed the clinical significance of copy number gain and loss at 5q21 approximately q23 combined with allelic loss of 3p25 (including the VHL gene). Fifty RCCs were examined by dual-color fluorescence in situ hybridization with DNA probes for D3Z1 (3cen), cCI3-865 (3p25.1 approximately p25.3), D5S23 (5p15.2), cCI5-243 (5q21.2 approximately q21.3), and cCI5-215 (5q22.3 approximately q23.2). In patients who had 3p loss, there was a significant association of loss at 5q22.3 approximately q23.2 with large tumors (>7 cm) and high-grade tumors (both P < 0.05), whereas gain at 5q22.3 approximately q23.2 was associated with low-grade tumors (P < 0.05). There was also a significant association loss at 5q21.2 approximately q21.3 high-grade tumors in patients with 3p loss (P < 0.05). Patients with 3p loss and gain at 5q22.3 approximately q23.2 had a significantly better disease-specific survival than those who had 3p loss without such gain (P < 0.05). Allelic loss of 3p25 including the VHL gene is thought to be an immediate event in the development of conventional RCC. Copy number gains or losses of 5q21 approximately q23 are thought to be events that lead to tumor progression although the clinical significance of either gains or losses is not well known.
对于传统肾细胞癌(RCC)中3p缺失与5q获得/缺失频繁关联的临床意义,人们了解甚少。我们分析了5q21至q23区域拷贝数增加和减少与3p25等位基因缺失(包括VHL基因)相结合的临床意义。采用针对D3Z1(3号染色体着丝粒)、cCI3 - 865(3p25.1至p25.3)、D5S23(5p15.2)、cCI5 - 243(5q21.2至q21.3)和cCI5 - 215(5q22.3至q23.2)的DNA探针,通过双色荧光原位杂交对50例肾细胞癌进行检测。在存在3p缺失的患者中,5q22.3至q23.2区域的缺失与大肿瘤(>7 cm)和高级别肿瘤显著相关(P均<0.05),而5q22.3至q23.2区域的获得与低级别肿瘤相关(P<0.05)。在存在3p缺失的患者中,5q21.2至q21.3区域的缺失与高级别肿瘤也显著相关(P<0.05)。存在3p缺失且5q22.3至q23.2区域获得的患者,其疾病特异性生存率显著高于存在3p缺失但无此获得的患者(P<0.05)。包括VHL基因在内的3p25等位基因缺失被认为是传统肾细胞癌发生过程中的早期事件。5q21至q23区域的拷贝数增加或减少被认为是导致肿瘤进展的事件,尽管其增加或减少的临床意义尚不明确。