Del Sal G, Collavin L, Ruaro M E, Edomi P, Saccone S, Valle G D, Schneider C
Laboratoire Nazionale, Consorzio Interuniversitario per le Biotechnologie, Trieste, Italy.
Proc Natl Acad Sci U S A. 1994 Mar 1;91(5):1848-52. doi: 10.1073/pnas.91.5.1848.
We describe the isolation, growth-suppressing activity, and chromosomal localization of the human homologue of the murine growth-arrest-specific gene gas1. Overexpression of h-gas1 is able to block cell proliferation in the A549 lung carcinoma and the T24 bladder carcinoma cell lines. No effect was observed when h-gas1 was introduced into the osteosarcoma cell line SAOS-2 and into the adenovirus-type-5 transformed cell line 293. This finding is related to our previous evidence that simian virus 40-transformed NIH 3T3 cells are also refractory to murine gas1 overexpression, suggesting that the retinoblastoma and/or p53 gene products have an active role in mediating the growth-suppressing effect of gas1. We also show that h-gas1 is on chromosome 9q21.3-22.1, in a region considered to be a fragile site. Altogether, the results raise the possibility that h-gas1 may be a target for genetic alterations leading to its inactivation in tumor cells.
我们描述了小鼠生长停滞特异性基因gas1的人类同源物的分离、生长抑制活性及染色体定位。h-gas1的过表达能够阻断A549肺癌细胞系和T24膀胱癌细胞系中的细胞增殖。将h-gas1导入骨肉瘤细胞系SAOS-2和腺病毒5型转化细胞系293时未观察到效果。这一发现与我们之前的证据相关,即猿猴病毒40转化的NIH 3T3细胞对小鼠gas1的过表达也具有抗性,提示视网膜母细胞瘤和/或p53基因产物在介导gas1的生长抑制作用中发挥积极作用。我们还表明,h-gas1位于9号染色体的q21.3 - 22.1区域,该区域被认为是一个脆性位点。总之,这些结果增加了h-gas1可能是导致其在肿瘤细胞中失活的基因改变靶点的可能性。