Otero-Estévez Olalla, De Chiara Loretta, Rodríguez-Girondo Mar, Rodríguez-Berrocal Francisco Javier, Cubiella Joaquín, Castro Inés, Hernández Vicent, Martínez-Zorzano Vicenta Soledad
Department of Biochemistry, Genetics and Immunology, Universidade de Vigo. Vigo, Spain.
SiDOR Research Group &Centro de Investigaciones Biomédicas (CINBIO), Universidade de Vigo. Vigo, Spain.
Sci Rep. 2015 Aug 12;5:13030. doi: 10.1038/srep13030.
Matrix metalloproteinase-9 (MMP-9) is related to tumour development and progression in colorectal cancer (CRC) and its utility as biomarker has been suggested. The aim of our study was to measure serum MMP-9 in asymptomatic first-degree relatives of CRC patients, and to analyse its diagnostic accuracy for the detection of advanced neoplasia (AN: advanced adenomas and CRC). Additionally, we compared its diagnostic capability with the most used non-invasive faecal immunochemical test (FIT). Serum MMP-9 was quantified by ELISA in 516 asymptomatic individuals that underwent a colonoscopy and a FIT. MMP-9 levels were significantly related to age and gender and therefore the concentration was corrected by these confounders. Corrected MMP-9 (cMMP-9) levels were higher in individuals with advanced adenomas (AA; p-value = 0.029) and AN (p-value = 0.056) compared to individuals with no neoplasia. Moreover, elevated cMMP-9 concentration was associated with more severe characteristics of adenomas (number of lesions, size and histology). Nevertheless, the diagnostic accuracy of cMMP-9 was considerably lower than that of FIT for identifying AA (22.64% vs. 47.17% sensitivity, 90% specificity) or AN (19.30% vs. 52.63% sensitivity, 90% specificity). According to our results, serum MMP-9 cannot be considered of utility for the diagnosis of AN in CRC family-risk population screening.
基质金属蛋白酶-9(MMP-9)与结直肠癌(CRC)的肿瘤发生和进展相关,并且有人提出其作为生物标志物的用途。我们研究的目的是测量CRC患者无症状的一级亲属血清中的MMP-9,并分析其对检测高级别瘤变(AN:高级别腺瘤和CRC)的诊断准确性。此外,我们将其诊断能力与最常用的非侵入性粪便免疫化学检测(FIT)进行了比较。通过酶联免疫吸附测定法(ELISA)对516名接受结肠镜检查和FIT的无症状个体的血清MMP-9进行了定量。MMP-9水平与年龄和性别显著相关,因此通过这些混杂因素对浓度进行了校正。与无瘤变的个体相比,高级别腺瘤(AA;p值 = 0.029)和AN(p值 = 0.056)个体的校正MMP-9(cMMP-9)水平更高。此外,cMMP-9浓度升高与腺瘤更严重的特征(病变数量、大小和组织学)相关。然而,cMMP-9在识别AA(敏感性:22.64%对47.17%,特异性90%)或AN(敏感性:19.30%对52.63%,特异性90%)方面的诊断准确性远低于FIT。根据我们的结果,在CRC家族风险人群筛查中,血清MMP-9不能被认为对AN的诊断有用。