Berenson J R, Koga H, Yang J, Pearl J, Holmes E C, Figlin R
Department of Medicine, UCLA School of Medicine-VAMC West Los Angeles 90024.
Oncogene. 1990 Sep;5(9):1343-8.
The bcl-1 locus on chromosome 11 at band q13 has been shown to be rearranged in some chronic B lymphoid malignancies with the t(11;14)(q13;q32). Chromosome 11 abnormalities occur in solid tumors including squamous cell cancers and adenocarcinomas. We have recently reported the frequency amplification of the bcl-1 locus in squamous cell carcinomas of head and neck origin, and increased copy number also has been found in some breast adenocarcinomas. In this investigation, we analyzed the arrangement, copy number and expression of this locus in 111 primary non-small cell lung cancers. Bcl-1 was found to be amplified three- to 10-fold in seven fresh tumors. Whereas none of 51 adenocarcinomas showed bcl-1 amplification, six of 46 squamous cell carcinomas revealed an increase in bcl-1 copy number. This amplification was more frequently associated with larger and more poorly differentiated tumors. None of the cancers showed rearrangement of this locus.
11号染色体q13带上的bcl-1基因座已被证明在一些伴有t(11;14)(q13;q32)的慢性B淋巴细胞恶性肿瘤中发生了重排。11号染色体异常出现在包括鳞状细胞癌和腺癌在内的实体瘤中。我们最近报道了头颈部来源的鳞状细胞癌中bcl-1基因座的频率扩增,并且在一些乳腺腺癌中也发现了拷贝数增加。在本研究中,我们分析了111例原发性非小细胞肺癌中该基因座的排列、拷贝数和表达情况。在7例新鲜肿瘤中发现bcl-1扩增了3至10倍。51例腺癌中均未显示bcl-1扩增,而46例鳞状细胞癌中有6例显示bcl-1拷贝数增加。这种扩增更常与更大且分化程度更低的肿瘤相关。所有癌症均未显示该基因座的重排。