改良培养方法对多发性骨髓瘤染色体核型检出率的影响

Nan Wang, Ke-Ke Fan, Li-Jun Yuan, Hong-Shi Jin, Li-Li Wang
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引用次数: 0

摘要

目的:探讨一种改进的培养方法进行核型分析,提高多发性骨髓瘤(MM)患者细胞遗传学异常的检出率,为MM患者的临床诊断、预后分层和个体化治疗提供更有力的信息。方法:80例新诊断的MM患者分为两组。观察组在培养液中添加IL-6 (10 ng/ml)和GM-CSF (30 ng/ml),对照组不添加刺激因子。两组样品在相同条件下培养72 h,用g带分析核型。比较两组细胞遗传学异常的检出率及相应特征。结果:观察组染色体畸变检出率较对照组显著提高,总检出率分别为72.5%和22.5%,≤60岁亚组为80.0%和19.2%,> 60岁亚组为68.0%和28.6%,差异有统计学意义(p)改良培养方法,加入IL-6 (10 ng/ml)和GM-CSF (30 ng/ml)双刺激因子孵育72小时,可有效提高MM患者异常核型检出率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The Effect of Improved Culturing Method on the Detection Rate of Chromosome Karyotyping in Multiple Myeloma].

Objective: To investigate an improved culturing method for karyotyping analysis, and increase the detection rate of cytogenetic abnormalities in patients with multiple myeloma (MM), so as to provide more powerful information for the clinical diagnosis, prognosis stratification, and individualized treatment of MM patients.

Methods: Eighty newly-diagnosed MM patients were enrolled and divided into two groups. In observation group, IL-6 (10 ng/ml) and GM-CSF (30 ng/ml) were supplemented in the culture medium, while no stimulating factor was added in control group. The samples from both groups were cultured for 72 hours under the same conditions, and their karyotypes were analyzed by G-banding. The detection rate of the cytogenetic abnormalities, as well as the corresponding characteristics were compared between the two groups.

Results: The detection rate of the chromosome aberrations was greatly increased in the observation group compared with the control group, the overall detection rate was 72.5% and 22.5%, respectively, as well as 80.0% and 19.2% in the subgroup of ≤60 years old, 68.0% and 28.6% in the subgroup of > 60 years old, which showed significant statistical differences (P<0.05).

Conclusion: The modification of the culturing method with the addition of IL-6 (10 ng/ml) and GM-CSF (30 ng/ml) dual stimulating factors followed by incubation for 72 hours can effectively increase the detection rate of abnormal karyotypes in MM patients.

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