Assessment Of Soluble Fas Ligand In Patients With Chronic Myeloid Leukemia

Sahar Radhi Yasir
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Abstract

Background: Soluble FasL (sFasL) generating from Membrane-bound FasL (mFasL) cleaved by matrix metalloproteinases (MMPs). sFasL inhibits the apoptotic and inflammatory activity of mFasL because of sFasL competes with the mFasL and binds to Fas. To evaluate serum soluble Fas ligand (sFasL) level in patients with chronic myeloid leukemia. Materials and Method: Serum levels of sFasL were measured by ELISA method after venous blood was collected from 56 CML patients (newly diagnosed and optimally treated) and 28 healthy subjects as control group. Results: There were no significant increases in serum sFasL patient compared to healthy control with P=0.07. When the mean sFasL concentration was obviously highest in newly diagnosed (216.9pg/ml) followed by healthy control (152.5pg/ml) and lowest in optimally treated (147.7 pg/ml). Conclusion: Production of sFasL in tumor patients may be a key mechanism to inhibit Fas-mediated apoptosis.  
慢性髓系白血病患者可溶性Fas配体的评估
背景:可溶性FasL (sFasL)是由基质金属蛋白酶(MMPs)裂解的膜结合FasL (mFasL)产生的。sFasL抑制mFasL的凋亡和炎症活性,因为sFasL与mFasL竞争并与Fas结合。目的探讨慢性髓系白血病患者血清可溶性Fas配体(sFasL)水平。材料与方法:采用ELISA法检测56例CML患者(新确诊、治疗最佳)和28例健康对照者静脉血后血清sFasL水平。结果:患者血清sFasL与健康对照组相比无显著升高(P=0.07)。sFasL的平均浓度在新诊断患者中最高(216.9pg/ml),其次是健康对照组(152.5pg/ml),在最佳治疗组中最低(147.7 pg/ml)。结论:肿瘤患者体内sFasL的产生可能是抑制fas介导的细胞凋亡的关键机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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