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B淋巴细胞慢性淋巴细胞白血病中的肿瘤抑制基因与克隆进化

Tumor suppressor genes and clonal evolution in B-CLL.

作者信息

Kay N E, Ranheim E A, Peterson L C

机构信息

University of Kentucky Medical Center, Markey Cancer Center, Lexington, USA.

出版信息

Leuk Lymphoma. 1995 Jun;18(1-2):41-9. doi: 10.3109/10428199509064921.

Abstract

This review highlights the genetic alterations that have been detailed in the malignant B-cell clones of patients with B-chronic lymphocytic leukemia (CLL). In particular, the alterations seen in p53 and the retinoblastoma (Rb) genes are reviewed. In addition, the multiplicity of cytogenetic alterations observed at baseline and on sequential analysis are summarized. The cytogenetic and molecular biologic analysis of B-CLL clones has revealed that there is a dynamic array of genetic events which occur within a B-cell clone. This latter data strongly suggests that clonal evolution may occur in B-CLL patients. However the relationship of the clonal instability to the patient's clinical course is still unclear. The relatively frequent detection of multiple tumor suppressor gene alterations in the B-CLL clones offer several interesting clues regarding the transformation event within B-CLL. A model is proposed which attempts to explain the potential contribution and interaction of p53 and Rb gene alterations in a malignant B-cell transformation.

摘要

本综述重点介绍了在B细胞慢性淋巴细胞白血病(CLL)患者恶性B细胞克隆中已详细描述的基因改变。特别回顾了p53和视网膜母细胞瘤(Rb)基因中所见的改变。此外,总结了在基线和序贯分析中观察到的细胞遗传学改变的多样性。B-CLL克隆的细胞遗传学和分子生物学分析表明,在B细胞克隆内发生了一系列动态的基因事件。后一项数据强烈表明,B-CLL患者可能发生克隆进化。然而,克隆不稳定性与患者临床病程之间的关系仍不清楚。在B-CLL克隆中相对频繁地检测到多个肿瘤抑制基因改变,为B-CLL内的转化事件提供了几个有趣的线索。提出了一个模型,试图解释p53和Rb基因改变在恶性B细胞转化中的潜在作用和相互作用。

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