De Angelis P M, Clausen O P, Schjølberg A, Stokke T
Institute of Pathology, The Norwegian National Hospital, Oslo.
Br J Cancer. 1999 May;80(3-4):526-35. doi: 10.1038/sj.bjc.6690388.
Comparative genomic hybridization (CGH) is used to detect amplified and/or deleted chromosomal regions in tumours by mapping their locations on normal metaphase chromosomes. Forty-five sporadic colorectal carcinomas were screened for chromosomal aberrations using direct CGH. The median number of chromosomal aberrations per tumour was 7.0 (range 0-19). Gains of 20q (67%) and losses of 18q (49%) were the most frequent aberrations. Other recurrent gains of 5p, 6p, 7, 8q, 13q, 17q, 19, X and losses of 1p, 3p, 4, 5q. 6q, 8p, 9p, 10, 15q, 17p were found in > 10% of colorectal tumours. High-level gains (ratio > 1.5) were seen only on 8q, 13q, 20 and X, and only in DNA aneuploid tumours. DNA aneuploid tumours had significantly more chromosomal aberrations (median number per tumour of 9.0) compared to diploid tumours (median of 1.0) (P < 0.0001). The median numbers of aberrations seen in DNA hyperdiploid and highly aneuploid tumours were not significantly different (8.5 and 11.0 respectively; P = 0.58). Four tumours had no detectable chromosomal aberrations and these were DNA diploid. A higher percentage of tumours from male patients showed Xq gain and 18q loss compared to tumours from female patients (P = 0.05 and 0.01 respectively). High tumour S phase fractions were associated with gain of 20q13 (P = 0.03), and low tumour apoptotic indices were associated with loss of 4q (P = 0.05). Tumours with TP53 mutations had more aberrations (median of 9.0 per tumour) compared to those without (median of 2.0) (P = 0.002), and gain of 8q23-24 and loss of 18qcen-21 were significantly associated with TP53 mutations (P = 0.04 and 0.02 respectively). Dukes' C/D stage tumours tended to have a higher number of aberrations per tumour (median of 10.0) compared to Dukes' B tumours (median of 3.0) (P = 0.06). The low number of aberrations observed in DNA diploid tumours compared to aneuploid tumours suggests that genomic instability and possible growth advantages in diploid tumours do not result from acquisition of gross chromosomal aberrations but rather from selection for other types of mutations. Our study is consistent with the idea that these two groups of tumours evolve along separate genetic pathways and that gross genomic instability is associated with TP53 gene aberrations.
比较基因组杂交(CGH)通过将肿瘤中扩增和/或缺失的染色体区域定位在正常中期染色体上,来检测这些区域。使用直接CGH对45例散发性结直肠癌进行染色体畸变筛查。每个肿瘤的染色体畸变中位数为7.0(范围0 - 19)。20q增益(67%)和18q缺失(49%)是最常见的畸变。其他常见的增益包括5p、6p、7、8q、13q、17q、19、X,缺失包括1p、3p、4、5q、6q、8p、9p、10、15q、17p,在超过10%的结直肠癌中被发现。高水平增益(比率>1.5)仅见于8q、13q、20和X,且仅在DNA非整倍体肿瘤中出现。与二倍体肿瘤(中位数为1.0)相比,DNA非整倍体肿瘤具有显著更多的染色体畸变(每个肿瘤中位数为9.0)(P < 0.0001)。DNA超二倍体和高度非整倍体肿瘤中观察到的畸变中位数无显著差异(分别为8.5和11.0;P = 0.58)。4个肿瘤未检测到染色体畸变,这些肿瘤为DNA二倍体。与女性患者的肿瘤相比,男性患者的肿瘤中显示Xq增益和18q缺失的比例更高(分别为P = 0.05和0.01)。高肿瘤S期分数与20q13增益相关(P = 0.03),低肿瘤凋亡指数与4q缺失相关(P = 0.05)。与无TP53突变的肿瘤(中位数为2.0)相比,有TP53突变的肿瘤具有更多的畸变(每个肿瘤中位数为9.0)(P = 0.002),8q23 - 24增益和18qcen - 21缺失与TP53突变显著相关(分别为P = 0.04和0.02)。与Dukes' B期肿瘤(中位数为3.0)相比,Dukes' C/D期肿瘤每个肿瘤的畸变数量往往更高(中位数为10.0)(P = 0.06)。与非整倍体肿瘤相比,DNA二倍体肿瘤中观察到较低的畸变数量,这表明二倍体肿瘤中的基因组不稳定性和可能的生长优势并非源于获得大量染色体畸变,而是源于对其他类型突变的选择。我们的研究与这两组肿瘤沿着不同遗传途径演变以及基因组总体不稳定性与TP53基因畸变相关的观点一致。