Frontiers in Immunology (May 2023)

Construction of a fecal immune-related protein-based biomarker panel for colorectal cancer diagnosis: a multicenter study

  • Hao Zhang,
  • Lugen Zuo,
  • Lugen Zuo,
  • Jing Li,
  • Jing Li,
  • Zhijun Geng,
  • Zhijun Geng,
  • Sitang Ge,
  • Sitang Ge,
  • Xue Song,
  • Xue Song,
  • Yueyue Wang,
  • Yueyue Wang,
  • Xiaofeng Zhang,
  • Xiaofeng Zhang,
  • Lian Wang,
  • Tianhao Zhao,
  • Tianhao Zhao,
  • Min Deng,
  • Min Deng,
  • Damin Chai,
  • Qiusheng Wang,
  • Zi Yang,
  • Quanli Liu,
  • Quanwei Qiu,
  • Xuxu He,
  • Yiqun Yang,
  • Yuanyuan Ge,
  • Rong Wu,
  • Lin Zheng,
  • Jianjun Li,
  • Runkai Chen,
  • Jialiang Sun,
  • Jianguo Hu,
  • Jianguo Hu

DOI
https://doi.org/10.3389/fimmu.2023.1126217
Journal volume & issue
Vol. 14

Abstract

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PurposeTo explore fecal immune-related proteins that can be used for colorectal cancer (CRC) diagnosis.Patients and methodsThree independent cohorts were used in present study. In the discovery cohort, which included 14 CRC patients and 6 healthy controls (HCs), label-free proteomics was applied to identify immune-related proteins in stool that could be used for CRC diagnosis. Exploring potential links between gut microbes and immune-related proteins by 16S rRNA sequencing. The abundance of fecal immune-associated proteins was verified by ELISA in two independent validation cohorts and a biomarker panel was constructed that could be used for CRC diagnosis. The validation cohort I included 192 CRC patients and 151 HCs from 6 different hospitals. The validation cohort II included 141 CRC patients, 82 colorectal adenoma (CRA) patients, and 87 HCs from another hospital. Finally, the expression of biomarkers in cancer tissues was verified by immunohistochemistry (IHC).ResultsIn the discovery study, 436 plausible fecal proteins were identified. And among 67 differential fecal proteins (|log2 fold change| > 1, P< 0.01) that could be used for CRC diagnosis, 16 immune-related proteins with diagnostic value were identified. The 16S rRNA sequencing results showed a positive correlation between immune-related proteins and the abundance of oncogenic bacteria. In the validation cohort I, a biomarker panel consisting of five fecal immune-related proteins (CAT, LTF, MMP9, RBP4, and SERPINA3) was constructed based on the least absolute shrinkage and selection operator (LASSO) and multivariate logistic regression. The biomarker panel was found to be superior to hemoglobin in the diagnosis of CRC in both validation cohort I and validation cohort II. The IHC result showed that protein expression levels of these five immune-related proteins were significantly higher in CRC tissue than in normal colorectal tissue.ConclusionA novel biomarker panel consisting of fecal immune-related proteins can be used for the diagnosis of CRC.

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