Prognostic values of myeloid differentiation factor 88 (MYD88) and transducin (β)-like receptor 1 (TBLR1) expression in tissues of diffuse large B-cell non-Hodgkin lymphoma patients – an immunohistochemical study

A. H. Mohamed, M. Elfeky, S. Elshorbagy, Nabila Hefzi, T. Oraby, W. Abdelhady, Mahmoud Sharaf Eldein, Ahmed Embaby, E. Oraby
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引用次数: 1

Abstract

Introduction Diffuse large B-cell non- Hodgkin lymphoma (DLBCL) is the largest common category of adult lymphoma. Recurrence and treatment resistance occurs in one-third of cases, triggering them to the progressive stage of DLBCL after treatment. Detection of novel predictive and prognostic biomarkers leads to improvement of its treatment and prognosis. Aim of the study To assess the prognostic roles of protein expression of myeloid differentiation factor 88 (MYD88) and transducin (β)-like receptor 1 (TBLR1) in tissues of DLBCL patients. Material and methods In the current study we included tissues from 100 cases of DLBCL. For immunohistochemistry, tissues were stained with MYD88 and TBLR1. We followed patients for about 3 years, and then we correlated their expression with clinicopathological and prognostic parameters. Results Higher MYD88 and TBLR1 expressions were associated with presence of B symptoms, fever, night sweat, advanced stage, bone marrow involvement and bulky nodal size, presence of extra-nodal extension, unfavourable relapse-free survival, and unfavourable overall survival rates (p < 0.001). Conclusions overexpression of MYD88 and TBLR1 expression was present in DLBCL patients and was associated with unfavourable clinicopathological and prognostic parameters.
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弥漫性大b细胞非霍奇金淋巴瘤患者组织中髓样分化因子88 (MYD88)和转导蛋白(β)样受体1 (TBLR1)表达的预后价值——一项免疫组织化学研究
弥漫性大b细胞非霍奇金淋巴瘤(DLBCL)是成人淋巴瘤中最常见的一类。三分之一的病例出现复发和治疗抵抗,使其在治疗后进入DLBCL的进展阶段。检测新的预测和预后的生物标志物导致其治疗和预后的改善。目的探讨髓样分化因子88 (MYD88)和转导蛋白(β)样受体1 (TBLR1)蛋白在DLBCL患者组织中的表达对预后的影响。材料和方法在本研究中,我们纳入了100例DLBCL的组织。免疫组化用MYD88和TBLR1染色。我们对患者进行了大约3年的随访,然后我们将他们的表达与临床病理和预后参数联系起来。结果MYD88和TBLR1的高表达与B型症状、发热、盗汗、晚期、骨髓受累和淋巴结肿大、淋巴结外延伸、不利的无复发生存和不利的总生存率相关(p < 0.001)。结论MYD88和TBLR1表达过表达存在于DLBCL患者中,并与不利的临床病理和预后参数相关。
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