Ichikawa T, Nihei N, Suzuki H, Oshimura M, Emi M, Nakamura Y, Hayata I, Isaacs J T, Shimazaki J
Department of Urology, School of Medicine, Chiba University, Japan.
Cancer Res. 1994 May 1;54(9):2299-302.
In previous allelotype analyses of human prostatic cancer specimens, allelic loss on the short arm of chromosome 8 is frequently observed. However, it is still unclear whether this allelic loss is an initial event or a later one in development of prostatic cancer. Our previous studies demonstrate that introduction of human chromosome 11 into highly metastatic rat prostatic cancer cells results in suppression of metastatic ability without suppression of the in vivo growth rate or tumorigenicity of the hybrid cells (T. Ichikawa et al. Cancer Res., 52: 3486-3490, 1992). To clarify the role of human chromosome 8 in prostatic cancer, this chromosome was introduced into highly metastatic rat prostatic cancer cells using microcell-mediated chromosome transfer. Introduction of human chromosome 8 resulted in suppression of metastatic ability of the microcell hybrids, whereas no suppression of the in vivo growth rate or tumorigenicity was observed. These results demonstrate that human chromosome 8 contains metastasis suppressor gene(s) for prostatic cancer derived from a rat. These also suggest that human chromosome 8 has an important role in development of prostatic cancer.
在先前对人类前列腺癌标本的等位基因分型分析中,经常观察到8号染色体短臂上的等位基因缺失。然而,这种等位基因缺失在前列腺癌发展过程中是早期事件还是晚期事件仍不清楚。我们先前的研究表明,将人类11号染色体导入高转移性大鼠前列腺癌细胞会导致转移能力受到抑制,而不会抑制杂交细胞在体内的生长速率或致瘤性(T. 市川等人,《癌症研究》,52: 3486 - 3490,1992)。为了阐明人类8号染色体在前列腺癌中的作用,使用微细胞介导的染色体转移将该染色体导入高转移性大鼠前列腺癌细胞。导入人类8号染色体导致微细胞杂交体的转移能力受到抑制,而未观察到体内生长速率或致瘤性受到抑制。这些结果表明,人类8号染色体含有源自大鼠的前列腺癌转移抑制基因。这些结果还表明,人类8号染色体在前列腺癌的发展中具有重要作用。