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Combined detection of plasma GATA5 and SFRP2 methylation is a valid noninvasive biomarker for colorectal cancer and adenomas

机译:血浆GATA5和SFRP2甲基化的联合检测是结直肠癌和腺瘤的有效无创生物标志物

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摘要

AIM: To investigate GATA5, SFRP2, and ITGA4 methylation in plasma DNA as noninvasive biomarkers for colorectal cancer (CRC) or adenomas.METHODS: There were 57 CRC patients, 30 adenomas patients, and 47 control patients enrolled in this study. Methylation-specific polymerase chain reaction was used to determine the promoter methylation status of GATA5, SFRP2, and ITGA4 genes in plasma DNA, and their association with clinical outcome in CRC. The predictive ability of GATA5, SFRP2, and ITGA4 methylation, individually or in combination, to detect CRC or adenomas was further analyzed.RESULTS: Hypermethylated GATA5 was detected in plasma in 61.4% (35/57) of CRC cases, 43.33% (13/30) of adenoma cases, and 21.28% (10/47) of control cases. The hypermethylation of SFRP2 was detected in 54.39% (31/57), 40.00% (12/30), and 27.66% (13/47) in plasma samples from CRC, adenomas, and controls, respectively. ITGA4 methylation was detected in 36.84% (21/57) of plasma samples of CRC patients and in 30.00% (9/30) of plasma samples from patients with colorectal adenomas, and the specificity of this individual biomarker was 80.85% (9/47). Moreover, GATA5 methylation in the plasma was significantly correlated with larger tumor size (P = 0.019), differentiation status (P = 0.038), TNM stage (P = 0.008), and lymph node metastasis (P = 0.008). SFRP2 and ITGA4 methylation in plasma significantly correlated with differentiation status (SFRP2, P = 0.012; ITGA4, P = 0.007), TNM stage (SFRP2, P = 0.034; ITGA4, P = 0.021), and lymph node metastasis (SFRP2, P = 0.034; ITGA4, P = 0.021). From the perspective of predictive power and cost-performance, using GATA5 and SFRP2 together as methylation markers seemed the most favorable predictor for CRC (OR = 8.06; 95%CI: 2.54-25.5; P < 0.01) and adenomas (OR = 3.35; 95%CI: 1.29-8.71; P = 0.012).CONCLUSION: A combination of GATA5 and SFRP2 methylation could be promising as a marker for the detection and diagnosis of CRC and adenomas.
机译:目的:探讨血浆DNA中GATA5,SFRP2和ITGA4甲基化作为结直肠癌(CRC)或腺瘤的非侵入性生物标志物的方法。方法:本研究共纳入57例CRC患者,30例腺瘤患者和47例对照患者。甲基化特异性聚合酶链反应用于确定血浆DNA中GATA5,SFRP2和ITGA4基因的启动子甲基化状态,以及它们与CRC临床结果的关系。进一步分析了单独或组合使用GATA5,SFRP2和ITGA4甲基化检测CRC或腺瘤的预测能力。结果:在血浆中检出高甲基化的GATA5的比例为61.4%(35/57),占43.33%(13) / 30)的腺瘤病例和21.28%(10/47)的对照病例。在来自CRC,腺瘤和对照的血浆样品中,分别检测到SFRP2的甲基化率高达54.39%(31/57),40.00%(12/30)和27.66%(13/47)。在结直肠腺瘤患者的血浆样本中,有36.84%(21/57)和30.00%(9/30)血浆样本中检测到ITGA4甲基化,该生物标志物的特异性为80.85%(9/47) )。此外,血浆中的GATA5甲基化与更大的肿瘤大小(P = 0.019),分化状态(P = 0.038),TNM分期(P = 0.008)和淋巴结转移(P = 0.008)显着相关。血浆中SFRP2和ITGA4甲基化与分化状态(SFRP2,P = 0.012; ITGA4,P = 0.007),TNM分期(SFRP2,P = 0.034; ITGA4,P = 0.021)和淋巴结转移(SFRP2,P = 0.034; ITGA4,P = 0.021)。从预测能力和性价比的角度来看,将GATA5和SFRP2一起用作甲基化标记似乎是CRC(OR = 8.06; 95%CI:2.54-25.5; P <0.01)和腺瘤(OR = 3.35; 95%CI:1.29-8.71; P = 0.012)。结论:GATA5和SFRP2甲基化的组合有望成为检测和诊断CRC和腺瘤的标志物。

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