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首页> 外文期刊>Journal of Clinical Oncology >MicroRNA signature obtained from the comparison of aggressive with indolent non-Hodgkin lymphomas: potential prognostic value in mantle-cell lymphoma.
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MicroRNA signature obtained from the comparison of aggressive with indolent non-Hodgkin lymphomas: potential prognostic value in mantle-cell lymphoma.

机译:从侵袭性和惰性非霍奇金淋巴瘤的比较中获得的MicroRNA签名:套细胞淋巴瘤的潜在预后价值。

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摘要

Mantle-cell lymphoma (MCL) has a variable natural history but is incurable with current therapies. MicroRNAs (miRs) are useful in prognostic assessment of cancer. We determined an miR signature defining aggressiveness in B-cell non-Hodgkin lymphomas (NHL) and assessed whether this signature aids in MCL prognosis.We assessed miR expression in a training set of 43 NHL cases. The miR signature was validated in 44 additional cases and examined on a training set of 119 MCL cases from four institutions in Canada. miRs significantly associated with overall survival were examined in an independent cohort of 114 MCL cases to determine association with patient outcome. miR expression was combined with current clinical prognostic factors to develop an enhanced prognostic model in patients with MCL.Fourteen miRs were differentially expressed between aggressive and indolent NHL; 11 of 14 were validated in an independent set of NHL (excluding MCL). miR-127-3p and miR-615-3p were significantly associated with overall survival in the MCL training set. Their expression was validated in an independent MCL patient set. In comparison with Ki-67, expression of these miRs was more significantly associated with overall survival among patients with MCL. miR-127-3p was combined with Ki-67 to create a new prognostic model for MCL. A similar model was created with miR-615-3p and Mantle Cell Lymphoma International Prognostic Index scores.Eleven miRs are differentially expressed between aggressive and indolent NHL. Two novel miRs were associated with overall survival in MCL and were combined with clinical prognostic models to generate novel prognostic data for patients with MCL.
机译:幔细胞淋巴瘤(MCL)具有可变的自然病史,但目前的治疗方法无法治愈。 MicroRNA(miRs)可用于癌症的预后评估。我们确定了miR信号定义了B细胞非霍奇金淋巴瘤(NHL)的侵袭性,并评估了该信号是否有助于MCL预后。我们在43例NHL病例中对miR表达进行了评估。 miR签名在另外44个案例中得到验证,并在来自加拿大四个机构的119个MCL案例的培训集中进行了检查。在114例MCL病例的独立队列中检查了与总体生存率显着相关的miR,以确定与患者预后的相关性。 miR的表达与目前的临床预后因素相结合,以建立增强的MCL患者预后模型。侵袭性和惰性NHL差异表达14个miR;在独立的一组NHL(不包括MCL)中验证了14个中的11个。在MCL训练集中,miR-127-3p和miR-615-3p与总体生存率显着相关。他们的表达在独立的MCL患者组中得到验证。与Ki-67相比,这些miR的表达与MCL患者的总体生存率显着相关。将miR-127-3p与Ki-67结合使用以创建MCL的新预后模型。用miR-615-3p和Mantle细胞淋巴瘤国际预后指数评分创建了相似的模型.11个miR在侵略性和惰性NHL之间差异表达。两种新颖的miR与MCL的整体生存率相关,并与临床预后模型结合以产生MCL患者的新预后数据。

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