Ichikawa T, Ichikawa Y, Isaacs J T
Johns Hopkins Oncology Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231.
Cancer Res. 1991 Jul 15;51(14):3788-92.
Progression of prostatic cancer from nonmetastatic to high metastatic ability may involve the loss of a metastasis suppressor gene. To test this possibility, nonmetastatic and highly metastatic Dunning rat prostatic cancer cells were fused. Hybrid clones were isolated which conserved the chromosomes from their parental cells. When these hybrids were injected into animals, none developed distant metastases. When these nonmetastatic primary tumors were passaged in vivo, occasional animals developed distant metastases. Cytogenetic analysis of eight of these metastatic revertants demonstrated a consistent loss of a copy of a normal chromosome 2. Although previous studies have demonstrated that specific chromosomes can inhibit tumorigenicity in cell fusion experiments, this is the first study to show that prostatic cancer metastasis is associated with the loss of a specific chromosome. Furthermore, these studies suggest that a metastasis suppressor gene for rat prostatic cancer is located on chromosome 2.
前列腺癌从非转移性发展到高转移能力可能涉及转移抑制基因的缺失。为了验证这种可能性,将非转移性和高转移性的邓宁大鼠前列腺癌细胞进行融合。分离出保留其亲代细胞染色体的杂交克隆。当将这些杂交细胞注射到动物体内时,没有一个发生远处转移。当这些非转移性原发性肿瘤在体内传代时,偶尔有动物发生远处转移。对其中八个转移性回复突变体的细胞遗传学分析表明,正常的2号染色体有一个拷贝持续缺失。尽管先前的研究表明特定染色体在细胞融合实验中可抑制肿瘤发生,但这是第一项表明前列腺癌转移与特定染色体缺失相关的研究。此外,这些研究表明大鼠前列腺癌的转移抑制基因位于2号染色体上。