Frontiers in Oncology (Apr 2021)

Feasibility of Methylated CLIP4 in Stool for Early Detection of Colorectal Cancer: A Training Study in Chinese Population

  • Yang Cao,
  • Yang Cao,
  • Guodong Zhao,
  • Guodong Zhao,
  • Guodong Zhao,
  • Yaping Cao,
  • Yaping Cao,
  • Zhiliang Chen,
  • Zhiliang Chen,
  • Xiaoyu Liu,
  • Mufa Yuan,
  • Mufa Yuan,
  • Jun Yang,
  • Jun Yang,
  • Xiaomei Wang,
  • Yong Ma,
  • Yong Ma,
  • Zhaocheng Liu,
  • Shangmin Xiong,
  • Shangmin Xiong,
  • Minxue Zheng,
  • Minxue Zheng,
  • Sujuan Fei,
  • Sujuan Fei

DOI
https://doi.org/10.3389/fonc.2021.647066
Journal volume & issue
Vol. 11

Abstract

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BackgroundEarly detection of colorectal cancer (CRC) and precancerous lesion is vitally important for mitigating CRC morbidity and mortality. Aberrant DNA methylations in certain promoter regions have been identified to be closely associated with CRC development and progression, suggesting their potential as diagnostic biomarkers for early detection. In this study, we evaluated the performance of methylated CLIP4 in stool specimens as a potential biomarker for CRC detection.MethodsA total of 321 subjects out of 365 enrolled participants were included in the final analysis, including 154 CRC patients, 23 advanced adenoma (AA) patients, 49 small polyp (SP) patients, and 95 healthy controls. CLIP4 methylation level was examined by qPCR with bisulfite converted DNA purified from approximately 5 g stool specimen.ResultsMethylated CLIP4 test showed high sensitivities of 78.3% (95% CI: 55.8%–91.7%) and 90.3% (95% CI: 84.2%–94.3%) for detecting AA and CRC, respectively, with a specificity of 88.4% (95% CI: 79.8%–93.8%). CLIP4 methylation level discriminated AA and CRC patients from control subjects with area under the curve values of 0.892 (95% CI: 0.795–0.988) and 0.961 (95% CI: 0.938–0.983). Further analysis indicated no significant difference in sensitivities among different ages, genders, stages, locations, sides, tumor sizes and differentiation statuses.ConclusionsMethylated CLIP4 showed a strong potential as a noninvasive biomarker for early CRC detection.

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