Atkin N B, Baker M C
Cancer. 1979 Aug;44(2):604-13. doi: 10.1002/1097-0142(197908)44:2<604::aid-cncr2820440230>3.0.co;2-g.
Cytogenetic studies on 26 carcinomas of the cervix showed that chromosome 1 was consistently involved in the changes: either one or more structurally abnormal chromosomes or a relative excess of normal chromosomes were present. Several types of structural change were repeatedly seen: short arm deletions (1p-, in seven tumors); long arm isochromosomes (i(1q), in six tumors); and translocations of unidentified chromosomal material onto one of the arms (possibly in eleven tumors; in four of these, there was an additional C-band on the long arm). In one tumor, there was a short arm isochromosome (i(1p)). The most consistent feature of the aneuploid complements of these tumors appeared to be the presence in excess of the centromeric region and at least part of the adjacent heterochromatin of chromosome 1.
对26例宫颈癌的细胞遗传学研究表明,1号染色体始终参与这些变化:存在一条或多条结构异常的染色体,或者正常染色体相对过量。反复观察到几种类型的结构变化:短臂缺失(1p-,7例肿瘤);长臂等臂染色体(i(1q),6例肿瘤);以及不明染色体物质易位到其中一条臂上(可能在11例肿瘤中;其中4例在长臂上有额外的C带)。在1例肿瘤中,存在短臂等臂染色体(i(1p))。这些肿瘤非整倍体补体最一致的特征似乎是1号染色体着丝粒区域及至少部分相邻异染色质的过量存在。