Suppr超能文献

埃及非霍奇金淋巴瘤患者基质金属蛋白酶-2单核苷酸多态性:与临床病理特征及预后的相关性

Matrix Metalloproteinase-2 Single Nucleotide Polymorphism in Egyptian Non-Hodgkin Lymphoma Patients: Correlation with Clinicopathological Characteristics and Outcome.

作者信息

Bakry Rania M, El-Gezawy Ebtesam M, Darwish Abeer M, NasrEldin Eman, Gaber Noha, Nasif Khalid A, El-Mohsen EssamAbd, Mahfouz Salma

机构信息

1Oncological Clinical Pathology Department, South Egypt Cancer Institute, Assiut University, Assiut, Egypt.

2Clinical Pathology Department, Faculty of Medicine, Assiut University, Assiut, Egypt.

出版信息

Indian J Hematol Blood Transfus. 2019 Jul;35(3):471-477. doi: 10.1007/s12288-018-1056-4. Epub 2018 Dec 7.

Abstract

Non-Hodgkin's lymphoma (NHL) is an exceedingly diversified group of lymphoproliferative neoplasms emerging from B-, T- or natural killer -lymphocytes. This study was done to detect Matrix metalloproteinase-2 (MMP2)-735C/T gene polymorphism in patients with NHL and its relation to the clinicopathological characteristics of the studied patients in addition to detection the association between it and NHL disease susceptibility and progression. Clinico-hematological profiles were done on 50 NHL patients. The genotypes and allelic frequencies of MMP-2 polymorphisms were recognized utilizing Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP). PCR products after adding restriction endonuclease were analyzed using QIAxcel advanced (automated) instrument. The CT + TT genotypes and T allele of MMP2 735C/T were statistically significant in patients having advanced clinical stages III/IV compared to patients with stages I/II. Another significance was observed in patients with intermediate high/high IPI score and BM infiltration. Interestingly, patients with MMP2-735C/T genotype exhibit lower rate of survival. Our results demonstrated that MMP2-735C/T polymorphism may potentially affect the progression of NHL. Further larger scale studies are needed.

摘要

非霍奇金淋巴瘤(NHL)是一组极其多样化的淋巴增殖性肿瘤,起源于B淋巴细胞、T淋巴细胞或自然杀伤淋巴细胞。本研究旨在检测NHL患者基质金属蛋白酶-2(MMP2)-735C/T基因多态性,及其与研究患者临床病理特征的关系,此外还检测其与NHL疾病易感性和进展的关联。对50例NHL患者进行了临床血液学检查。利用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)识别MMP-2多态性的基因型和等位基因频率。加入限制性内切酶后的PCR产物使用QIAxcel advanced(自动化)仪器进行分析。与I/II期患者相比,MMP2 735C/T的CT+TT基因型和T等位基因在临床晚期III/IV期患者中具有统计学意义。在中高/高国际预后指数(IPI)评分和骨髓浸润患者中也观察到另一个显著差异。有趣的是,具有MMP2-735C/T基因型的患者生存率较低。我们的结果表明,MMP2-735C/T多态性可能会影响NHL的进展。需要进一步开展更大规模的研究。

相似文献

本文引用的文献

2
Cancer treatment and survivorship statistics, 2014.癌症治疗和生存统计,2014 年。
CA Cancer J Clin. 2014 Jul-Aug;64(4):252-71. doi: 10.3322/caac.21235. Epub 2014 Jun 1.
7
Cancer statistics, 2013.癌症统计数据,2013 年。
CA Cancer J Clin. 2013 Jan;63(1):11-30. doi: 10.3322/caac.21166. Epub 2013 Jan 17.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验