Shimura Takaya, Iwasaki Hiroyasu, Kitagawa Mika, Ebi Masahide, Yamada Tamaki, Yamada Tomonori, Katano Takahito, Nisie Hirotada, Okamoto Yasuyuki, Ozeki Keiji, Mizoshita Tsutomu, Kataoka Hiromi
Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan.
Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya 467-8601, Japan.
Transl Oncol. 2019 Mar;12(3):539-544. doi: 10.1016/j.tranon.2018.12.006. Epub 2019 Jan 3.
Since a fecal occult blood test for colorectal cancer (CRC) does not offer sufficient diagnostic power for CRC, novel non-invasive biomarkers are hopeful for CRC screening. We conducted the current study to discover non-invasive urinary biomarkers for diagnosing CRC. Among urine samples from 258 patients (CRC, n = 148; healthy controls, n = 110), a cohort of 176 patients composed of 88 patients with GC and 88 healthy controls was selected after age- and sex-matching using propensity score. This cohort was then randomly divided into 2 groups: 53 pairs (106 patients) in the training cohort, and 35 pairs (70 patients) in the validation cohort. No significant differences were found for baseline characteristics between the CRC and healthy control groups in both training and validation cohorts. On multivariate analysis in the training cohort, urinary levels of cysteine-rich protein 61 (uCyr61) and trefoil factor 3 (uTFF3) were identified as independent significant diagnostic markers for CRC. Moreover, uCyr61 alone and the combination of uCyr61 and uTFF3 allowed significant differentiation between healthy controls and CRC groups in the training set (uCyr61: area under the curve (AUC) = 0.745 [95% CI, 0.653-0.838]; uCyr61 + uTFF3: AUC = 0.753 [95% CI, 0.659-0.847]). In the validation cohort, uCyr61 and uTFF3 were significantly higher in the CRC group than in the healthy control group, and they also allowed significant differentiation between healthy control and CRC groups (uCyr61: AUC = 0.696 [95% CI, 0.571-0.822]; uTFF3: AUC = 0.639 [95% CI, 0.508-0.770]; uCyr61 + uTFF3: AUC = 0.720 [95% CI, 0.599-0.841]), as in the training cohort. A panel combining uCyr61 and uTFF3 offers a promising non-invasive biomarker for diagnosing CRC.
由于用于结直肠癌(CRC)的粪便潜血试验对CRC的诊断能力不足,新型非侵入性生物标志物有望用于CRC筛查。我们开展了本研究以发现用于诊断CRC的非侵入性尿液生物标志物。在258例患者(CRC患者148例;健康对照者110例)的尿液样本中,使用倾向评分法按年龄和性别匹配后,选取了由88例胃癌患者和88例健康对照者组成的176例患者队列。然后将该队列随机分为2组:训练队列中的53对(106例患者)和验证队列中的35对(70例患者)。在训练队列和验证队列中,CRC组与健康对照组之间的基线特征均未发现显著差异。在训练队列的多变量分析中,富含半胱氨酸的蛋白61(uCyr61)和三叶因子3(uTFF3)的尿液水平被确定为CRC的独立显著诊断标志物。此外,单独的uCyr61以及uCyr61与uTFF3的组合在训练集中能够显著区分健康对照组和CRC组(uCyr61:曲线下面积(AUC)=0.745 [95%CI,0.653 - 0.838];uCyr61 + uTFF3:AUC =0.753 [95%CI,0.659 - 0.847])。在验证队列中,CRC组的uCyr61和uTFF3显著高于健康对照组,它们也能够显著区分健康对照组和CRC组(uCyr61:AUC =0.696 [95%CI,0.571 - 0.822];uTFF3:AUC =0.639 [95%CI,0.508 - 0.770];uCyr61 + uTFF3:AUC =0.720 [95%CI,0.599 - 0.841]),与训练队列情况相同。结合uCyr61和uTFF3的检测组合为诊断CRC提供了一种有前景的非侵入性生物标志物。