R2TP复合体RUVBL1组分的表达与DLBCL不良预后相关

Moien Lone, Mahaiwon Shadang, Qulsum Akhter, Mithilesh Kumar, Saumyaranjan Mallick, Ajay Gogia, Nilima Nilima, Shyam S Chauhan, Riyaz A Mir
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引用次数: 2

摘要

漫漫性大b细胞淋巴瘤(DLBCL)是最常见的非霍奇金淋巴瘤(NHL)亚型,占全球成人NHL的30%,在印度等发展中国家占50%。DNA损伤和myc诱导的转化是众所周知的促进DLBCL发展的因素。最近发现的HSP90共同伴侣复合体R2TP已被证明有助于DNA损伤和myc诱导的转化。本研究旨在分析R2TP复合物RUVBL1、PIH1D1和RPAP3在DLBCL患者中的免疫组化表达及其与预后的关系。方法:从档案中检索DLBCL (n = 54)的组织学切片,记录详细的组织形态学和临床特征。对54例DLBCL患者(FFPE)进行R2TP复合物RUVBL1、PIH1D1、RPAP3的免疫组化染色。表达数据与生存和临床特征相关。结果:54例DLBCL中,59.26% (n = 32) RUVBL1染色阳性。在无进展生存期(PFS) (p = 0.0146)和总生存期(OS) (p = 0.0328)中,RUVBL1表达与不良预后相关。表达与骨髓受累程度呈正相关(p = 0.0525)。PIH1D1在68.51% (n = 32)的DLBCL患者中表达,与国际预后指数评分呈正相关(p = 0.0246);但与PFS或OS无相关性。最后,RPAP3仅在1例DLBCL中呈免疫阳性。结论:RUVBL1免疫阳性与DLBCL患者预后差以及复发率高相关。PIH1D1免疫阳性与较高的IPI评分相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Expression of the RUVBL1 Component of the R2TP Complex Correlates with Poor Prognosis in DLBCL.

Introduction: Diffuse large B-cell lymphoma (DLBCL) is the most prevalent subtype of non-Hodgkin's lymphoma (NHL) accounting for 30% of adult NHL worldwide and 50% in developing countries like India. DNA damage and Myc-induced transformation are well-known contributing factors towards development of DLBCL. A recently identified HSP90 co-chaperone complex R2TP has been shown to contribute towards DNA damage and Myc-induced transformation. This study aimed to analyse the immunohistochemical (IHC) expression of R2TP complex components RUVBL1, PIH1D1, and RPAP3 in DLBCL patients and correlate with prognosis.

Methods: DLBCL (n = 54) histological slides were retrieved from archives, and detailed histomorphological and clinical features were noted. IHC staining of R2TP complex components RUVBL1, PIH1D1, and RPAP3 was performed on 54 cases (FFPE) of DLBCL. Expression data were correlated with survival and clinical features.

Results: Out of the 54 DLBCL cases, 59.26% (n = 32) stained positive for RUVBL1. The RUVBL1 expression was associated with poor prognosis in both progression-free survival (PFS) (p = 0.0146) and overall survival (OS) (p = 0.0328). The expression was positively correlated with bone marrow involvement (p = 0.0525). The expression of PIH1D1 was observed in 68.51% (n = 32) of DLBCL cases, and positive correlation was observed with international prognostic index score (p = 0.0246); however, no correlation was observed with PFS or OS. Finally, RPAP3 was found immunopositive in only 1 case of DLBCL.

Conclusions: Immunopositivity for RUVBL1 is associated with poor prognosis along with a higher relapse rate amongst the DLBCL patients. PIH1D1 immunopositivity correlated with a higher IPI score.

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