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Serum angiopoietin-like protein 2 as a potential biomarker for diagnosis, early recurrence and prognosis in gastric cancer patients

机译:血清血管生成素样蛋白2作为胃癌患者诊断,早期复发和预后的潜在生物标志物

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Chronic inflammation of gastric mucosa by Helicobacter pylori infection can initiate gastric carcinogenesis. As angiopoietinlike protein 2 (ANGPTL2) mediates inflammation and inflammation-associated carcinogenesis, we investigated the functional and clinical significance of ANGPTL2 in human gastric cancer (GC). SiRNA knockdown studies were performed for the functional assessment of ANGPTL2 in GC cell lines. ANGPTL2 expression was evaluated immunohistochemically in 192 tissue specimens from GC patients. In addition, we screened serum ANGPTL2 levels from 32 GC patients and 23 healthy controls; and validated these results in 194 serum samples from GC patients and 45 healthy controls by ELISA. ANGPTL2 knockdown caused anoikis and inhibited proliferation, invasion and migration in GC cells. ANGPTL2 expression was upregulated in GC tissues compared to normal gastric mucosa; and high ANGPTL2 expression was significantly associated with tumor progression, early recurrence (P = 0.003) and poor prognosis (P = 0.007). Serum ANGPTL2 in GC patients was significantly higher than for healthy controls (P < 0.05), and accurately distinguished GC patients from healthy control (AUC = 0.865). The validation step confirmed significantly higher serum ANGPTL2 levels in GC patients than healthy controls (P < 0.0001). Receiver operating characteristic curves yielded robust AUC value (0.831) accompanied by high sensitivity (73.0%) and specificity (82.2%) in distinguishing GC patients from healthy controls. High serum ANGPTL2, rather than its expression in matched tissues, was significantly associated with tumor progression, and emerged as an independent marker for recurrence (HR: 5.05, P = 0.0004) and prognosis (HR: 3.6, P = 0.01). Serum ANGPTL2 expression is a potential noninvasive biomarker for diagnosis, early recurrence and prognosis of GC patients.
机译:幽门螺杆菌感染引起的胃粘膜慢性炎症可引发胃癌发生。由于血管生成素样蛋白2(ANGPTL2)介导炎症和炎症相关的致癌作用,我们调查了ANGPTL2在人胃癌(GC)中的功能和临床意义。进行了SiRNA敲低研究,以评估GC细胞系中ANGPTL2的功能。免疫组化在GC患者的192个组织标本中评估了ANGPTL2的表达。此外,我们从32名GC患者和23名健康对照者中筛选了血清ANGPTL2水平。并通过ELISA在来自GC患者的194个血清样品和45个健康对照中验证了这些结果。 ANGPTL2敲低引起神经过敏并抑制GC细胞的增殖,侵袭和迁移。与正常胃粘膜相比,GC组织中ANGPTL2表达上调。 ANGPTL2高表达与肿瘤进展,早期复发(P = 0.003)和不良预后(P = 0.007)显着相关。 GC患者的血清ANGPTL2显着高于健康对照组(P <0.05),并能准确地区分GC患者与健康对照组(AUC = 0.865)。验证步骤证实,GC患者的血清ANGPTL2水平明显高于健康对照组(P <0.0001)。接收器工作特征曲线可产生可靠的AUC值(0.831),同时具有高灵敏度(73.0%)和特异性(82.2%),可将GC患者与健康对照区分开。高血清ANGPTL2,而不是其在匹配组织中的表达,与肿瘤进展显着相关,并作为复发(HR:5.05,P = 0.004)和预后(HR:3.6,P = 0.01)的独立标志物出现。血清ANGPTL2表达是GC患者诊断,早期复发和预后的潜在非侵入性生物标志物。

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    《Carcinogenesis》 |2015年第12期|共10页
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  • 正文语种 eng
  • 中图分类 肿瘤学;
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