Lambers A R, Gumbs C, Ali S, Marks J R, Iglehart J D, Berchuck A, Futreal P A
Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA.
Br J Cancer. 1999 Jul;80(10):1575-6. doi: 10.1038/sj.bjc.6690564.
The recently described Bcl10 gene has been suggested to be a major target gene for inactivation in a variety of human cancers. In order to further evaluate the role of this gene in human adult malignancies, we have analysed a series of carcinomas for mutations in the Bcl10 gene. We have screened a panel of 174 carcinoma samples in total, comprised of 47 breast, 36 epithelial ovarian, 36 endometrial, 12 cervical, 23 colorectal and 20 head/neck carcinomas, all unselected for grade or stage. This panel reflects, in part, tumours reported to have involvement of the 1p22 region of chromosome 1, the region harbouring the Bcl10 gene. No deleterious mutations were detected in any of the samples analysed, strongly suggesting that Bcl10 is not a common target for inactivation in adult malignancies and that BCL10 is not the gene targeted for frequent inactivation at 1p22.
最近描述的Bcl10基因被认为是多种人类癌症中失活的主要靶基因。为了进一步评估该基因在人类成人恶性肿瘤中的作用,我们分析了一系列癌组织中Bcl10基因的突变情况。我们总共筛选了174个癌组织样本,包括47个乳腺癌、36个上皮性卵巢癌、36个子宫内膜癌、12个宫颈癌、23个结直肠癌和20个头颈癌,所有样本均未根据分级或分期进行筛选。该样本组部分反映了据报道涉及1号染色体1p22区域(即携带Bcl10基因的区域)的肿瘤。在所分析的任何样本中均未检测到有害突变,这强烈表明Bcl10不是成人恶性肿瘤中失活的常见靶基因,且BCL10不是1p22处频繁失活的靶基因。