Champème M H, Bièche I, Beuzelin M, Lidereau R
Laboratoire d'Oncogénétique, Centre René Huguenin, Saint-Cloud, France.
Genes Chromosomes Cancer. 1995 Apr;12(4):304-6. doi: 10.1002/gcc.2870120411.
Although human breast tumorigenesis is associated with the accumulation of mutations both in oncogenes and in tumor suppressor genes, the identity of the genetic alterations that are critical in the early stages of the breast tumorigenic process remains obscure. A high frequency (27-41%) of loss of heterozygosity (LOH) occurrence has been shown at the MET locus on chromosome band 7q31 and this specific alteration is associated with poorer survival. Here, we report that restriction fragment length polymorphism (RFLP) analysis on 221 informative (heterozygous) primary breast tumors and 57 informative relapses (13 local recurrences and 44 distant metastases) revealed a similar frequency of 7q31 LOH as tumors progress from primary cancer to relapse, in marked contrast to other changes such as 11p15.5 LOH. This finding suggests that inactivation of a putative tumor suppressor gene located in 7q31 is a very early event in breast tumorigenesis. Our results also show that metastatic potential is an induced phenomenon that occurs at a relatively early stage, rather than a marker of tumor progression.
虽然人类乳腺肿瘤发生与癌基因和肿瘤抑制基因中的突变积累相关,但在乳腺肿瘤发生过程早期起关键作用的基因改变的具体情况仍不清楚。已显示在染色体7q31带上的MET位点杂合性缺失(LOH)发生率很高(27 - 41%),且这种特定改变与较差的生存率相关。在此,我们报告对221例信息丰富(杂合)的原发性乳腺肿瘤和57例信息丰富的复发肿瘤(13例局部复发和44例远处转移)进行的限制性片段长度多态性(RFLP)分析显示,随着肿瘤从原发性癌症发展到复发,7q31 LOH的频率相似,这与其他改变如11p15.5 LOH形成显著对比。这一发现表明位于7q31的一个假定肿瘤抑制基因的失活是乳腺肿瘤发生中非常早期的事件。我们的结果还表明转移潜能是一种在相对早期发生的诱导现象,而非肿瘤进展的标志。