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血液系统恶性肿瘤中的性染色体丢失与拟常染色体区域基因

Sex chromosome loss and the pseudoautosomal region genes in hematological malignancies.

作者信息

Weng Stephanie, Stoner Samuel A, Zhang Dong-Er

机构信息

Moores Cancer Center, University of California San Diego, La Jolla, CA, USA.

Department of Pathology and Division of Biological Sciences, University of California San Diego, La Jolla, CA, USA.

出版信息

Oncotarget. 2016 Nov 1;7(44):72356-72372. doi: 10.18632/oncotarget.12050.

Abstract

Cytogenetic aberrations, such as chromosomal translocations, aneuploidy, and amplifications, are frequently detected in hematological malignancies. For many of the common autosomal aberrations, the mechanisms underlying their roles in cancer development have been well-characterized. On the contrary, although loss of a sex chromosome is observed in a broad range of hematological malignancies, how it cooperates in disease development is less understood. Nevertheless, it has been postulated that tumor suppressor genes reside on the sex chromosomes. Although the X and Y sex chromosomes are highly divergent, the pseudoautosomal regions are homologous between both chromosomes. Here, we review what is currently known about the pseudoautosomal region genes in the hematological system. Additionally, we discuss implications for haploinsufficiency of critical pseudoautosomal region sex chromosome genes, driven by sex chromosome loss, in promoting hematological malignancies. Because mechanistic studies on disease development rely heavily on murine models, we also discuss the challenges and caveats of existing models, and propose alternatives for examining the involvement of pseudoautosomal region genes and loss of a sex chromosome in vivo. With the widespread detection of loss of a sex chromosome in different hematological malignances, the elucidation of the role of pseudoautosomal region genes in the development and progression of these diseases would be invaluable to the field.

摘要

细胞遗传学异常,如染色体易位、非整倍体和扩增,在血液系统恶性肿瘤中经常被检测到。对于许多常见的常染色体异常,其在癌症发生中作用的潜在机制已得到充分表征。相反,尽管在广泛的血液系统恶性肿瘤中都观察到性染色体缺失,但其在疾病发展中如何协同作用却知之甚少。然而,据推测肿瘤抑制基因位于性染色体上。尽管X和Y性染色体高度不同,但假常染色体区域在两条染色体之间是同源的。在这里,我们综述了目前关于血液系统中假常染色体区域基因的已知情况。此外,我们讨论了由性染色体缺失导致的关键假常染色体区域性染色体基因单倍体不足在促进血液系统恶性肿瘤中的影响。由于对疾病发展的机制研究严重依赖于小鼠模型,我们还讨论了现有模型的挑战和注意事项,并提出了在体内研究假常染色体区域基因和性染色体缺失参与情况的替代方法。随着在不同血液系统恶性肿瘤中广泛检测到性染色体缺失,阐明假常染色体区域基因在这些疾病发生和发展中的作用对该领域将具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a9d/5342167/cbcb44779510/oncotarget-07-72356-g001.jpg

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