BCL2L12在急性白血病患者中的表达:与临床和预后因素的潜在关联

B. Hassan, A. Hossein, R. Hossein, Boroumand Noughabi Samaneh, G. Masoumeh, Alidadi Mohammad, Shajiei Arezoo, Sadeghian Mohammad Hadi
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引用次数: 0

摘要

细胞凋亡在生理和病理条件下都是重要的机制。BCL2蛋白家族在凋亡细胞死亡的调控中起关键作用。BCL2-like 12 (BCL2L12)是BCL2家族的一个新成员,已经在几种恶性肿瘤中报道过上调和下调。然而,BCL2L12在白血病中的表达水平很少被研究。本研究旨在探讨BCL2L12 mRNA在急性白血病患者中的表达。材料与方法:90例急性白血病患者为病例组,90例正常人为对照组。从外周血样本中提取RNA。采用实时定量聚合酶链反应(qRT-PCR)方法检测BCL2L12 mRNA的表达水平,并分析其与临床和实验室结果的相关性。结果:BCL2L12 mRNA在急性淋巴细胞白血病(ALL)患者中的表达明显低于对照组(P<0.001),而在急性髓性白血病(AML)患者中的表达与对照组相比无显著差异。此外,ALL患者的BCL2L12水平在女性(高于男性)和t患者(12;21)中均较高。BCL2L12表达水平与AML患者的其他临床和实验室结果无相关性。结论:BCL2L12可能参与ALL的发病机制。需要更大样本量的进一步研究来阐明其对预后和治疗的可能影响
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Expression of BCL2L12 in acute leukemia patients: Potential association with clinical and prognostic factors
Introduction: Apoptosis is an important mechanism in both physiological and pathological conditions. The BCL2 family of proteins plays a critical role in regulation of apoptotic cell death. Up and down regulation of BCL2-like 12 (BCL2L12), a new member of the BCL2 family, has been reported in several malignancies. However, the expression level of BCL2L12 rarely has been studied in leukemia. This study was designed to investigate the mRNA expression of BCL2L12 in patients with acute leukemia. Materials and methods: 90 patients with acute leukemia as case group and 90 healthy persons as controls, were participated this study. RNA was extracted from peripheral blood samples. Expression level of BCL2L12 mRNA was evaluated by a quantitative real-time polymerase chain reaction (qRT-PCR) method and its association with clinical and laboratory findings was analyzed. Results: The expression of BCL2L12 mRNA was significantly lower in acute lymphoblastic leukemia (ALL) cases comparing the controls (P<0.001), while it was not significantly different in acute myeloid leukemia (AML) samples compared the control group. In addition, there were higher BCL2L12 level in females (than in males) and in patients with t(12;21) in ALL patients. There was no association between BCL2L12 expression level and other clinical and laboratory findings of AML patients. Conclusion: BCL2L12 seems play a role in the pathogenesis of ALL. Further studies with larger sample size is needed to clarify its probable impact on prognosis and therapeutic
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