Center R, Lukeis R, Vrazas V, Garson O M
Department of Cytogenetics, St. Vincent's Hospital, Fitzroy, Victoria, Australia.
Int J Cancer. 1993 Sep 30;55(3):390-3. doi: 10.1002/ijc.2910550309.
While loss of the Y chromosome from the karyotype of tumor cells has frequently been found in a number of human malignancies of different types, structural alterations are a much less common finding. Prompted by the high frequency of cytogenetic Y chromosome loss found in primary non-small-cell lung cancer (NSCLC), and the fact that NSCLC karyotypes usually contain marker chromosomes of unidentified origin, we have determined the Y chromosome status of 12 NSCLC samples (7 cell lines and 5 primary tumors) at a molecular level. Of the 9 cases which did not have a cytogenetically detectable Y chromosome, 4 were negative for all the Y sequences tested. The other 5, in contrast, retained some Y chromosome sequences. In 1 case (H520), only Yq heterochromatic sequences were detected, whereas in the remaining 4 (L162, L93, L125 and L71) both Yq heterochromatic sequences and Y euchromatic sequences were retained. The region of common overlap for loss of Y euchromatin was Yp distal to the Y centromere. We hypothesize that deletion of Yp sequences may play a role in tumor progression in NSCLC due to loss of a tumor-suppressor gene.
虽然在多种不同类型的人类恶性肿瘤中经常发现肿瘤细胞核型中Y染色体缺失,但结构改变的发现则要少得多。受原发性非小细胞肺癌(NSCLC)中细胞遗传学Y染色体缺失的高频率以及NSCLC核型通常包含来源不明的标记染色体这一事实的启发,我们在分子水平上确定了12个NSCLC样本(7个细胞系和5个原发性肿瘤)的Y染色体状态。在9例细胞遗传学检测未发现Y染色体的病例中,4例对所有检测的Y序列均为阴性。相比之下,其他5例保留了一些Y染色体序列。在1例(H520)中,仅检测到Yq异染色质序列,而在其余4例(L162、L93、L125和L71)中,Yq异染色质序列和Y常染色质序列均被保留。Y常染色质缺失的共同重叠区域位于Y着丝粒远端的Yp。我们假设Yp序列的缺失可能由于肿瘤抑制基因的丢失而在NSCLC的肿瘤进展中起作用。