Theillet C, Adnane J, Szepetowski P, Simon M P, Jeanteur P, Birnbaum D, Gaudray P
CNRS URA 1191 Centre Paul Lamarque, Montpellier, France.
Oncogene. 1990 Jan;5(1):147-9.
In an attempt to probe the significance of HST and INT-2 gene amplification in human breast carcinomas, we have surveyed the amplification status of five molecular markers located on the long arm of chromosome 11 (BCL-1, HST, INT-2 & SEA on 11q13, and ETS-1 on 11q23) in a population of 297 mammary tumors. ETS-1 was rarely amplified and always independently from the other proto-oncogenes. Concerning band q13: (i) 50 tumors (approximately 17%) were co-amplified for BCL-1, HST & INT-2; (ii) in 3 cases, amplification extended to the SEA gene; (iii) in 6 carcinomas, BCL-1 was the only amplified marker. The fact that we never observed amplification of HST & INT-2 independently of BCL-1, which in turn can be amplified solely, suggests the presence, between HST/INT-2 and BCL-1, of a genetic element which could be important in the development of a subset of mammary tumors.
为了探究HST和INT-2基因扩增在人类乳腺癌中的意义,我们在297例乳腺肿瘤群体中调查了位于11号染色体长臂上的五个分子标记(11q13上的BCL-1、HST、INT-2和SEA,以及11q23上的ETS-1)的扩增状态。ETS-1很少扩增,且总是独立于其他原癌基因。关于11q13带:(i)50例肿瘤(约17%)中BCL-1、HST和INT-2共同扩增;(ii)3例中扩增延伸至SEA基因;(iii)6例癌中,BCL-1是唯一扩增的标记。我们从未观察到HST和INT-2独立于BCL-1扩增,而BCL-1又可单独扩增,这一事实表明在HST/INT-2和BCL-1之间存在一个可能在一部分乳腺肿瘤发生中起重要作用的遗传元件。