Frontiers in Genetics (Aug 2022)

Comprehensive exploration of tumor immune microenvironment feature and therapeutic response in colorectal cancer based on a novel immune-related long non-coding RNA prognostic signature

  • Xueliang Zhou,
  • Xueliang Zhou,
  • Xueliang Zhou,
  • Batuer Aikemu,
  • Batuer Aikemu,
  • Shuchun Li,
  • Shuchun Li,
  • Yanfei Shao,
  • Yanfei Shao,
  • Yanfei Shao,
  • Hongtao Jia,
  • Hongtao Jia,
  • Hongtao Jia,
  • Ling Huang,
  • Ling Huang,
  • Ling Huang,
  • Hiju Hong,
  • Hiju Hong,
  • Sen Zhang,
  • Sen Zhang,
  • Sen Zhang,
  • Qiushi Tang,
  • Ruijun Pan,
  • Ruijun Pan,
  • Jing Sun,
  • Jing Sun,
  • Minhua Zheng,
  • Minhua Zheng

DOI
https://doi.org/10.3389/fgene.2022.962575
Journal volume & issue
Vol. 13

Abstract

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Colorectal cancer (CRC) is one of the most common malignant tumors with a high incidence rate and mortality. LncRNA is an important regulator of the immune system. It is of great significance to study immune-related lncRNAs (IR-lncRNAs) for CRC. In this study, we screened IR-lncRNAs differentially expressed in normal and CRC tissues, and Univariate Cox regression and the Least Absolute Shrinkage and Selection Operator were applied to construct IR-lncRNA prognostic signature in TCGA training dataset, and its predictive capability for the prognosis of CRC patients was verified in GSE39582 validation dataset. The novel signature was identified as an independent predictor of prognosis in CRC patients. In addition, the signature could accurately predict the feature of the immune microenvironment and therapeutic response in CRC patients. The CMap database was adopted to screen for small molecule candidate drugs that can reverse and treat high-risk CRC patients. Finally, the expression of six IR-lncRNAs were verified by qRT-PCR in clinical specimens from our patient cohort. In conclusion, we construct an IR-lncRNA prognostic signature, which is a powerful biomarker of CRC and can accurately predict the prognosis, immune microenvironment feature, and therapeutic response of CRC patients.

Keywords