Correlation between LRP1B Mutations and Tumor Mutation Burden in Gastric Cancer

Comput Math Methods Med. 2021 Sep 21:2021:1522250. doi: 10.1155/2021/1522250. eCollection 2021.

Abstract

Background: It has been shown that low-density lipoprotein receptor-related protein 1B (LRP1B) mutations correlate with tumor mutation burden (TMB) and prognosis in patients with melanoma and non-small-cell lung cancer, while the relationship between LRP1B mutations and TMB in gastric cancer needs further study. This study is aimed at exploring the relationship between LRP1B mutations and TMB in gastric cancer.

Methods: Mutation frequency profiles of the genes in patients with gastric cancer in TCGA-STAD dataset were analyzed by bioinformatics analysis. The relationship among LRP1B mutations, TMB, and patient clinical features in gastric cancer was investigated by the chi-square test. The TMB prediction capacity based on LRP1B mutation status was evaluated by ROC curves.

Results: LRP1B is one of the top 10 genes with high gene mutation frequency in gastric cancer. The mutation status of LRP1B in gastric cancer patients was significantly correlated with age and TP53 and MUC16 mutation status. The result of ROC curve analysis revealed that the mutation status of LRP1B could be considered as an indicator of the degree of TMB in patients with gastric cancer.

Conclusion: This study presented the relationship between TMB and LRP1B mutations in gastric cancer, providing a novel perspective for gastric cancer prognosis and therapy.

Publication types

  • Retracted Publication

MeSH terms

  • Biomarkers, Tumor / genetics*
  • CA-125 Antigen / genetics
  • Computational Biology
  • Databases, Genetic
  • Female
  • Gene Frequency
  • Genes, p53
  • Humans
  • Male
  • Membrane Proteins / genetics
  • Middle Aged
  • Mutation*
  • Prognosis
  • Receptors, LDL / genetics*
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology

Substances

  • Biomarkers, Tumor
  • CA-125 Antigen
  • LRP1B protein, human
  • MUC16 protein, human
  • Membrane Proteins
  • Receptors, LDL