Li Juan, Zhang Dian-Bao, Luo Shao-Kai, Zhao Ying, Huang Bei-Hui, Gu Jing-Li
Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510080, PR China.
Ai Zheng. 2007 Sep;26(9):1010-4.
BACKGROUND & OBJECTIVE: beta-catenin is the pivotal regulator in Wnt pathway and in charge of cellular adhesion and signal conduction. Overexpression of beta-catenin has been observed in various human tumors. This study was to investigate the expression and clinical significance of beta-catenin in multiple myeloma (MM).
Reverse transcription-polymerase chain reaction (RT-PCR) and Western blot were used to detect mRNA and protein expression of beta-catenin in bone marrow samples from 12 newly diagnosed MM patients, 14 relapsed/refractory MM patients, and 11 healthy donors. The clinical data and treatment outcomes of the MM patient were also analyzed.
The positive rate and the expression level of beta-catenin mRNA were significantly lower in healthy donors than in newly diagnosed patients and relapsed/refractory patients (27.3% vs. 75.0% and 100%, P=5.01e(-4); 0.35+/-0.17 vs. 0.72+/-0.11 and 0.85+/-0.16, P=5.88e(-5)); the mRNA level of beta-catenin was significantly lower in newly diagnosed patients than in relapsed/refractory patients (P=0.045). beta-catenin protein was not detected in healthy donors; while the positive rate and the expression level of beta-catenin protein were significantly lower in newly diagnosed patients than in relapsed/refractory patients (50.0% vs. 85.7%, 0.32+/-0.11 vs. 0.21+/-0.08, P=0.039). In the 10 newly diagnosed MM patients with evaluable treatment outcomes, the positive rate of beta-catenin protein was significant lower in the 7 patients without response than in the 3 patients showed response (14.3% vs. 100%, P=0.033). The positive rate of beta-catenin protein was significant higher in the 16 Durie/Salmon stage III patients than in the 10 stage II patients (87.5% vs. 40.0%, P=0.026), and significant higher in ISS stage III patients than in stage I and II patients (100% vs. 45.5% and 33.3%, P=0.006, P=0.032). The protein level of beta-catenin was positively correlated to serum levels of beta2-MG (r=0.688, P=0.002) and lactate dehydrogenase (LDH) (r=0.502, P=0.034).
The expression of beta-catenin is related with treatment outcome, Durin-Salmon stage and ISS stage of MM, and is positively correlated to serum levels of LDH and beta2-MG.
β-连环蛋白是Wnt信号通路中的关键调节因子,负责细胞黏附和信号传导。在多种人类肿瘤中均观察到β-连环蛋白的过表达。本研究旨在探讨β-连环蛋白在多发性骨髓瘤(MM)中的表达及临床意义。
采用逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测12例新诊断MM患者、14例复发/难治性MM患者及11例健康供者骨髓样本中β-连环蛋白的mRNA和蛋白表达。同时分析MM患者的临床资料及治疗结果。
健康供者中β-连环蛋白mRNA的阳性率及表达水平显著低于新诊断患者和复发/难治性患者(27.3% 对75.0% 和100%,P = 5.01e(-4);0.35±0.17对0.72±0.11和0.85±0.16,P = 5.88e(-5));新诊断患者中β-连环蛋白mRNA水平显著低于复发/难治性患者(P = 0.045)。健康供者未检测到β-连环蛋白蛋白;新诊断患者中β-连环蛋白蛋白的阳性率及表达水平显著低于复发/难治性患者(50.0% 对85.7%,0.32±0.11对0.21±0.08,P = 0.039)。在10例有可评估治疗结果的新诊断MM患者中,无反应的7例患者β-连环蛋白蛋白阳性率显著低于有反应的3例患者(14.3% 对100%,P = 0.033)。Durie/Salmon分期III期的16例患者中β-连环蛋白蛋白阳性率显著高于II期的10例患者(87.5% 对40.0%,P = 0.026),国际分期系统(ISS)III期患者显著高于I期和II期患者(100% 对45.5% 和33.3%,P = 0.006,P = 0.032)。β-连环蛋白蛋白水平与血清β2-微球蛋白(β2-MG)水平(r = 0.688,P = 0.002)和乳酸脱氢酶(LDH)水平(r = 0.502,P = 0.034)呈正相关。
β-连环蛋白的表达与MM的治疗结果、Durie-Salmon分期及ISS分期相关,且与血清LDH和β2-MG水平呈正相关。