Jin Y S, Heim S, Mandahl N, Biörklund A, Wennerberg J, Mitelman F
Department of Clinical Genetics, Lund University Hospital, Sweden.
Genes Chromosomes Cancer. 1990 Jan;1(3):209-15. doi: 10.1002/gcc.2870010304.
Short-term cultures from 12 oral squamous cell carcinomas were cytogenetically investigated. A normal karyotype was found in 3 tumors, 2 of which had many nonclonal changes. Clonal chromosome abnormalities were detected in the remaining 9 cases, in 6 of them in the form of 2 or 3 abnormal clones. In 5 cases the different clones were cytogenetically unrelated, suggesting a multiclonal origin. Numerous additional nonclonal changes were present in 4 of the 9 tumors with clonal aberrations. None of the structural aberrations, clonal or nonclonal, were found in more than one case; nor did any of the rearrangements correspond to cancer-associated aberrations known from other tumors. The aberration breakpoints of the present series and of previously reported tongue cancer clustered to bands 1p32, 1p22, 1p11, 1q21, 1q23, 1q25, 1q32, 1q42, 1q44, 2q31, 3p11, 4q35, 7p22, 11p15, 11q13, 12q24, and 17q25.
对12例口腔鳞状细胞癌的短期培养物进行了细胞遗传学研究。在3个肿瘤中发现了正常核型,其中2个有许多非克隆性改变。在其余9例中检测到克隆性染色体异常,其中6例表现为2个或3个异常克隆。在5例中,不同的克隆在细胞遗传学上不相关,提示多克隆起源。在9例有克隆畸变的肿瘤中,有4例存在许多额外的非克隆性改变。无论是克隆性还是非克隆性的结构畸变,均未在超过1例中发现;也没有任何重排与其他肿瘤已知的癌症相关畸变相对应。本系列以及先前报道的舌癌的畸变断点集中在1p32、1p22、1p11、1q21、1q23、1q25、1q32、1q42、1q44、2q31、3p11、4q35、7p22、11p15、11q13、12q24和17q25带。