CXCR4 overexpression in chronic lymphocytic leukemia associates with poorer prognosis: A prospective, single-center, observational study

IF 5 3区 医学 Q1 GENETICS & HEREDITY
Xinran Xue, Zhihao Wen, Xin Zhang, Ying Yang, Yifei Li, Ruoxi Liao, Qin Zheng, Yang Fu, Yu Liu, Hongyan Liao
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Abstract

Controversial data have been reported on the prognostic value of C-X-C motif chemokine receptor 4 (CXCR4) in chronic lymphocytic leukemia (CLL). This prospective, single-center, observational study aimed to evaluate the role of CXCR4 in the pathophysiology of CLL and its prognostic role. A total of 158 patients of CLL were enrolled, and CXCR4 expression on CLL cells was detected by flow cytometry (FCM) at initial diagnosis. The patients were divided into 2 groups according to the CXCR4 mean fluorescence intensity (MFI) median. Also, four patient specimens from the CXCR4low and CXCR4high groups were selected for RNASeq analysis. The progression-free survival (PFS) of CLL patients in the CXCR4high group was significantly shorter than the CXCR4low group, with a median follow-up time of 27 months (log-rank P < 0.001). Moreover, CXCR4 overexpression (MFI > 3376) was an independent marker of poor PFS in CLL patients (P < 0.001). Analysis of RNASeq results revealed that CXCR4 plays an important role in the migration of CLL. Collectively, CXCR4 expression levels on leukemia cells can be detected rapidly by FCM. CXCR4 overexpression was significantly associated with poorer prognosis in CLL patients within a shorter follow-up time.

Abstract Image

慢性淋巴细胞白血病中的 CXCR4 过度表达与较差的预后有关:一项前瞻性单中心观察研究。
关于 C-X-C motif 趋化因子受体 4(CXCR4)在慢性淋巴细胞白血病(CLL)中的预后价值,有争议的数据报道。这项前瞻性单中心观察性研究旨在评估 CXCR4 在 CLL 病理生理学中的作用及其预后作用。研究共招募了 158 名 CLL 患者,在初诊时通过流式细胞术(FCM)检测 CLL 细胞上的 CXCR4 表达。根据CXCR4平均荧光强度(MFI)中位数将患者分为两组。同时,从CXCR4低组和CXCR4高组中选择4例患者标本进行RNASeq分析。CXCR4high组CLL患者的无进展生存期(PFS)明显短于CXCR4low组,中位随访时间为27个月(对数秩P 3376),是CLL患者PFS差的独立标志(P
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来源期刊
Genes and immunity
Genes and immunity 医学-免疫学
CiteScore
8.90
自引率
4.00%
发文量
28
审稿时长
6-12 weeks
期刊介绍: Genes & Immunity emphasizes studies investigating how genetic, genomic and functional variations affect immune cells and the immune system, and associated processes in the regulation of health and disease. It further highlights articles on the transcriptional and posttranslational control of gene products involved in signaling pathways regulating immune cells, and protective and destructive immune responses.
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