Verma R S, Macera M J, Krishnamurthy M, Abramson J, Kapelner S, Dosik H
J Cancer Res Clin Oncol. 1987;113(2):192-6. doi: 10.1007/BF00391443.
Chromosomal studies were performed on six patients with adult T-cell leukemia (ATL). Structural abnormalities of chromosome 3 were the most common. In one case a complete loss of the short arm of chromosome 10 (10 p-) was noted while in another case a balanced translocation involving chromosome 10p and 4q was found. These abnormalities have not been previously reported. After reviewing the literature, it was concluded that chromosomes 3, 6, 10, 13, 14, and X were most frequently involved in abnormalities. Specific and consistent chromosomal abnormalities were noted in each study. Therefore, it is hypothesised that the mutation rate for this virus may be higher than first expected. Furthermore, the relative consistency of heterogeneous findings in different localities may reflect a geographic clustering of specific chromosomal abnormalities which may in turn be related to specific and geographically associated viral mutations. To support these suggestions not only are more cytogenetic data required but a molecular evaluation of these patients must be carried out to establish a relationship, if any, between genetic abnormalities and the epidemiology of ATL.
对6例成人T细胞白血病(ATL)患者进行了染色体研究。3号染色体的结构异常最为常见。1例患者发现10号染色体短臂完全缺失(10p-),另1例患者发现涉及10号染色体短臂和4号染色体长臂的平衡易位。这些异常情况此前未见报道。查阅文献后得出结论,3、6、10、13、14号染色体和X染色体最常出现异常。每项研究中均发现了特定且一致的染色体异常。因此,推测该病毒的突变率可能高于最初预期。此外,不同地区异质性研究结果的相对一致性可能反映了特定染色体异常的地理聚集性,而这反过来可能与特定的、与地理相关的病毒突变有关。为支持这些观点,不仅需要更多的细胞遗传学数据,还必须对这些患者进行分子评估,以确定遗传异常与ATL流行病学之间是否存在关联(若有)。