Immune landscape and prognostic immune-related genes in KRAS-mutant colorectal cancer patients

J Transl Med. 2021 Jan 7;19(1):27. doi: 10.1186/s12967-020-02638-9.

Abstract

Background: KRAS gene is the most common type of mutation reported in colorectal cancer (CRC). KRAS mutation-mediated regulation of immunophenotype and immune pathways in CRC remains to be elucidated.

Methods: 535 CRC patients were used to compare the expression of immune-related genes (IRGs) and the abundance of tumor-infiltrating immune cells (TIICs) in the tumor microenvironment between KRAS-mutant and KRAS wild-type CRC patients. An independent dataset included 566 cases of CRC and an in-house RNA sequencing dataset were served as validation sets. An in-house dataset consisting of 335 CRC patients were used to analyze systemic immune and inflammatory state in the presence of KRAS mutation. An immue risk (Imm-R) model consist of IRG and TIICs for prognostic prediction in KRAS-mutant CRC patients was established and validated.

Results: NF-κB and T-cell receptor signaling pathways were significantly inhibited in KRAS-mutant CRC patients. Regulatory T cells (Tregs) was increased while macrophage M1 and activated CD4 memory T cell was decreased in KRAS-mutant CRC. Prognosis correlated with enhanced Tregs, macrophage M1 and activated CD4 memory T cell and was validated. Serum levels of hypersensitive C-reactive protein (hs-CRP), CRP, and IgM were significantly decreased in KRAS-mutant compared to KRAS wild-type CRC patients. An immune risk model composed of VGF, RLN3, CT45A1 and TIICs signature classified CRC patients with distinct clinical outcomes.

Conclusions: KRAS mutation in CRC was associated with suppressed immune pathways and immune infiltration. The aberrant immune pathways and immune cells help to understand the tumor immune microenvironments in KRAS-mutant CRC patients.

Keywords: Colorectal cancer; Immunosuppression; KRAS mutation; Tumor-infiltrating immune cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Neoplasm
  • Colonic Neoplasms* / genetics
  • Colorectal Neoplasms* / genetics
  • Genes, ras
  • Humans
  • Mutation / genetics
  • Prognosis
  • Proto-Oncogene Proteins p21(ras) / genetics
  • Relaxin*
  • Tumor Microenvironment

Substances

  • Antigens, Neoplasm
  • CT45A1 protein, human
  • KRAS protein, human
  • RLN3 protein, human
  • Relaxin
  • Proto-Oncogene Proteins p21(ras)