首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Fc receptor-like 1-5 molecules are similarly expressed in progressive and indolent clinical subtypes of B-cell chronic lymphocytic leukemia.
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Fc receptor-like 1-5 molecules are similarly expressed in progressive and indolent clinical subtypes of B-cell chronic lymphocytic leukemia.

机译:Fc受体样1-5分子在B细胞慢性淋巴细胞性白血病的进行性和惰性临床亚型中相似地表达。

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摘要

Fc receptor-like (FCRL) 1-5 molecules are exclusively expressed in B-cells and have recently been considered as potential targets for immunotherapy of B-cell malignancies. In this study, the expression pattern of FCRL1-5 molecules was investigated in Iranian patients with B-cell chronic lymphocytic leukemia (B-CLL). Our RT-PCR results have demonstrated that all FCRL molecules, except FCRL4, were expressed in the vast majority of the patients with B-CLL. However, comparison of the relative mRNA expression levels of FCRL between B-CLL (n = 86) and elderly normal subjects (n = 10) revealed significantly lower expression levels of FCRL1 (p < 0.0001), FCRL3 (p = 0.01) and FCRL4 (p = 0.002), but not FCRL2 or FCRL5, in cases with B-CLL. No significant differences were observed between the indolent and progressive subtypes of patients with B-CLL. Comparison between the mutated and unmutated subtypes revealed a significantly higher expression level of FCRL3 (p = 0.017) in patients with mutated CLL. Surface and intracytoplasmic expression of FCRL1, 2, 4 and 5 in leukemic cells of 12 patients by flow cytometry revealed similar results to those obtained by RT-PCR with a few exceptions. Thus, while FCRL4 was expressed in only 2 samples at intracytoplasmic level, FCRL1 and 2 were expressed in the majority of samples, both at surface and intracytoplasm. FCRL5 protein was also detected in 10 samples, but surface expression was confirmed in only 2. Analysis of B-cells from 5 normal subjects by flow cytometry revealed higher expression levels of FCRL molecules compared to CLL. Our results indicate differential expression of FCRL molecules in B-CLL and suggest the potential implication of FCRL1 and 2 for immunotherapeutic interventions.
机译:Fc受体样(FCRL)1-5分子仅在B细胞中表达,最近被认为是B细胞恶性肿瘤免疫治疗的潜在靶标。在这项研究中,研究了FCRL1-5分子在伊朗B细胞慢性淋巴细胞性白血病(B-CLL)患者中的表达模式。我们的RT-PCR结果表明,除FCRL4外,所有FCRL分子均在绝大多数B-CLL患者中表达。然而,比较B-CLL(n = 86)和老年正常受试者(n = 10)之间FCRL的相对mRNA表达水平,发现FCRL1(p <0.0001),FCRL3(p = 0.01)和FCRL4的表达水平明显降低。 (p = 0.002),但在使用B-CLL的情况下,则不是(FCRL2或FCRL5)。 B-CLL患者的惰性和进行性亚型之间未观察到显着差异。突变亚型和未突变亚型之间的比较显示,在CLL突变患者中,FCRL3的表达水平明显更高(p = 0.017)。流式细胞术检测12例白血病细胞中FCRL1、2、4和5的表面和胞浆内表达,结果与RT-PCR相似,只有少数例外。因此,尽管FCRL4仅在两个样品中在胞浆内表达,而FCRL1和2在大多数样品中在表面和胞浆内表达。在10个样品中也检测到了FCRL5蛋白,但仅在2个样品中证实了表面表达。通过流式细胞术对5名正常受试者的B细胞进行分析显示,与CLL相比,FCRL分子的表达水平更高。我们的结果表明FCRL分子在B-CLL中的差异表达,并暗示FCRL1和2对免疫治疗干预的潜在影响。

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