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里氏综合征霍奇金变异型病例中MDR-1基因多态性G2677T和C3435T

MDR-1 gene polymorphisms G2677T and C3435T in a case of Hodgkin's variant of Richter's syndrome.

作者信息

Penna Giuseppa, Allegra Alessandro, Alonci Andrea, Aguennouz Mohamed, Cannavò Antonino, Russo Sabina, Granata Angela, Musolino Caterina

机构信息

Division of Hematology, Policlinico G. Martino, University of Messina, Messina, Italy.

出版信息

Oncol Lett. 2011 Mar;2(2):379-381. doi: 10.3892/ol.2011.243. Epub 2011 Jan 20.

Abstract

Richter's syndrome is defined as the transformation of low-grade lymphoma to a more aggressive high-grade malignant form, usually diffuse large B-cell lymphoma. Hodgkin's lymphoma variant of Richter transformation is relatively rare, and only approximately 100 cases have been reported in the literature. This study examined a case of a 53-year-old woman who developed Hodgkin's lymphoma almost 5 years after the diagnosis of chronic lymphocytic leukemia (CLL). The major points of interest regarding CLL with Hodgkin's transformation were also considered, such as the potential role of MDR-1 gene polymorphisms. The patient was evaluated for two MDR-1 gene polymorphisms, G2677T polymorphism in exon 21 and silent C3435T polymorphism in exon 26, to ascertain whether polymorphisms affect the risk of Hodgkin's lymphoma variant of Richter transformation and whether genomic polymorphisms provide prognostic information on the clinical progression of the disease. According to the data obtained, the analysis of polymorphisms in the MDR1 gene exons 21 and 26 revealed that the T2677T and T3435T alleles are not a predisposing factor to Richter transformation, while the presence of the wild-type genotype may be associated with a more favorable response to therapy.

摘要

里氏综合征被定义为低度淋巴瘤向更具侵袭性的高度恶性形式转变,通常为弥漫性大B细胞淋巴瘤。里氏转化的霍奇金淋巴瘤变体相对罕见,文献中仅报道了约100例。本研究检查了一例53岁女性病例,该患者在诊断为慢性淋巴细胞白血病(CLL)近5年后发生了霍奇金淋巴瘤。还考虑了CLL伴霍奇金转化的主要关注点,如MDR-1基因多态性的潜在作用。对患者进行了两种MDR-1基因多态性评估,即外显子21中的G2677T多态性和外显子26中的沉默C3435T多态性,以确定多态性是否影响里氏转化的霍奇金淋巴瘤变体风险,以及基因组多态性是否能为疾病的临床进展提供预后信息。根据获得的数据,对MDR1基因外显子21和26中的多态性分析表明,T2677T和T3435T等位基因不是里氏转化的易感因素,而野生型基因型的存在可能与对治疗的更有利反应相关。

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