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衍生(1;18)(q10;q10):一种在髓系疾病中涉及1q的复发性新型不平衡易位。

Derivative (1;18)(q10;q10): a recurrent and novel unbalanced translocation involving 1q in myeloid disorders.

作者信息

Wan T S, Ma S K, Au W Y, Chan L C

机构信息

Department of Pathology, The University of Hong Kong, Queen Mary Hospital, Pokfulam Road, Hong Kong, People's Republic of China.

出版信息

Cancer Genet Cytogenet. 2001 Jul 1;128(1):35-8. doi: 10.1016/s0165-4608(01)00391-0.

Abstract

We report two cases of hematological malignancies, comprising a case of myelodysplastic syndrome (MDS) that rapidly evolved into acute myeloid leukemia, and a case of myeloproliferative disorder (MPD), in which der(1;18)(q10;q10) was found as the sole acquired karyotypic abnormality. This observation indicates that the unbalanced translocation is a recurrent aberration in myeloid disorders. To the best of our knowledge, centromeric fusion between long arms of chromosomes 1 and 18, leading to a normal chromosome 18 substituted with a der(1;18) chromosome, is novel and has not been described in cancer. Mechanistically, either trisomy 1q or monosomy 18p that results from the translocation may potentially contribute to leukemogenesis. Finally, chromosomes with large constitutive heterochromatin bands such as chromosome 1 may be at risk of centromeric instability and be predisposed to centromeric fusion with other chromosomes.

摘要

我们报告了两例血液系统恶性肿瘤病例,其中一例为骨髓增生异常综合征(MDS),该病例迅速演变为急性髓系白血病;另一例为骨髓增殖性疾病(MPD),在该病例中发现der(1;18)(q10;q10)是唯一获得性核型异常。这一观察结果表明,不平衡易位是髓系疾病中一种反复出现的畸变。据我们所知,1号和18号染色体长臂之间的着丝粒融合,导致正常的18号染色体被der(1;18)染色体取代,这是新颖的,且在癌症中尚未有描述。从机制上讲,由易位导致的1q三体或18p单体可能潜在地促进白血病发生。最后,具有大的组成型异染色质带的染色体,如1号染色体,可能存在着丝粒不稳定的风险,并易于与其他染色体发生着丝粒融合。

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