Habashy Deena Mohamed, Eissa Deena Samir, Aboelez Mona Mahmoud
Ain Shams University Faculty of Medicine, Department of Clinical Pathology, Unit of Hematology, Cairo, Egypt
Turk J Haematol. 2018 Aug 3;35(3):168-174. doi: 10.4274/tjh.2017.0169. Epub 2017 Sep 8.
Traditional prognostic factors have proved insufficient to account for heterogeneity in the clinical behavior of chronic lymphocytic leukemia (CLL). -1 () is a circadian clock gene essential in maintaining the circadian rhythm and regulating cell proliferation. We evaluated gene expression in CLL and addressed its putative role as a prognostic indicator for the clinical course of CLL.
A total of 100 CLL patients at diagnosis were studied for gene expression by real-time reverse-transcription polymerase chain reaction and were followed for assessment of time to first treatment (TFT).
was expressed in 94% of the CLL patients at diagnosis. The median relative gene expression level (0.006) stratified patients into high and low expression groups. Forty of 100 (40%) CLL patients showed high , 54/100 (54%) showed low , and 6/100 (6%) had undetectable gene expression. High gene expression was concordant with CD38, Zap-70, and double CD38Zap-70 expression; unfavorable/intermediate cytogenetics; unmutated gene; and diffuse marrow infiltration. The high gene expression patient group exhibited shorter TFT than the patients with low gene expression. A Cox proportional hazard regression model identified gene expression to be independently predictive for TFT.
is differentially expressed among CLL patients, stratifying them into low-risk and high-risk groups. gene expression could constitute a reliable prognostic indicator for CLL progression, complementing the role of standard well-established prognostic factors. gene expression could be employed as a prognostic indicator for disease progression during the initial prognostic work-up and follow-up for CLL patients.
传统预后因素已被证明不足以解释慢性淋巴细胞白血病(CLL)临床行为的异质性。-1()是维持昼夜节律和调节细胞增殖所必需的昼夜节律基因。我们评估了CLL中该基因的表达,并探讨了其作为CLL临床病程预后指标的潜在作用。
共对100例初诊CLL患者进行研究,通过实时逆转录聚合酶链反应检测该基因的表达,并随访评估首次治疗时间(TFT)。
94%的初诊CLL患者表达该基因。根据相对基因表达水平中位数(0.006)将患者分为高表达组和低表达组。100例CLL患者中,40例(40%)显示高表达,54例(54%)显示低表达,6例(6%)检测不到该基因表达。高基因表达与CD38、Zap-70及CD38Zap-70双表达一致;细胞遗传学不良/中等;未突变基因;以及弥漫性骨髓浸润。高基因表达患者组的TFT短于低基因表达患者。Cox比例风险回归模型确定基因表达可独立预测TFT。
该基因在CLL患者中存在差异表达,将患者分为低风险和高风险组。基因表达可作为CLL进展的可靠预后指标,补充已确立的标准预后因素的作用。基因表达可在CLL患者的初始预后评估和随访期间用作疾病进展的预后指标。