Potentiality of α-fetoprotein (AFP) and soluble intercellular adhesion molecule-1 (sICAM-1) in prognosis prediction and immunotherapy response for patients with hepatocellular carcinoma

Bioengineered. 2021 Dec;12(2):9435-9451. doi: 10.1080/21655979.2021.1990195.

Abstract

ABSTRCTThe α-fetoprotein (AFP) and soluble intercellular adhesion molecule-1 (sICAM-1) have certain diagnostic value, but their potential value in prognosis prediction, especially immunotherapy response prediction, remains unclear in liver cancer. Through the tumor-free survival (TFS) and overall survival (OS) rates analyses of serum AFP and sICAM-1 levels in 87 patients with primary hepatocellular carcinoma (HCC), the patients whose AFP and sICAM-1 levels were normal (AFP < 20 μg/L or sICAM-1 < 1000 μg/L) before surgery or recovered to normal after surgery exhibited a lower tumor recurrence rate and better OS than patients with elevated serum levels of the two markers. Combined analysis showed that patients with synchronously elevated levels of AFP and sICAM-1 showed the lowest TFS and OS. In addition, the RNA-seq data and clinical information of The Cancer Genome Atlas Liver Hepatocellular Carcinoma were collected to analyze the predictive values of AFP and ICAM-1 in the diagnosis, prognosis and immunotherapy of HCC. The results indicated that the combined application of the two indicators had higher accuracy in both the diagnosis and prognostic prediction of HCC by receiver operating characteristic curves. AFP and ICAM-1 were significantly correlated with multiple immune cells in HCC samples but not in normal samples. The patients with low expression of the two indicators were most likely to benefit from the immune checkpoint blockade therapy. In conclusion, AFP and ICAM-1 play vital roles in the diagnosis, prognostic prediction, and immunotherapy of HCC, suggesting that they are considered as prognostic predictors in clinical practice.

Keywords: immunotherapy response; prognosis prediction; soluble intercellular adhesion molecule-1; α-fetoprotein.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't
  • Video-Audio Media

MeSH terms

  • Adult
  • Aged
  • Carcinoma, Hepatocellular* / blood
  • Carcinoma, Hepatocellular* / immunology
  • Carcinoma, Hepatocellular* / mortality
  • Carcinoma, Hepatocellular* / therapy
  • Disease-Free Survival
  • Female
  • Humans
  • Immunotherapy*
  • Intercellular Adhesion Molecule-1* / blood
  • Intercellular Adhesion Molecule-1* / immunology
  • Liver Neoplasms* / blood
  • Liver Neoplasms* / immunology
  • Liver Neoplasms* / mortality
  • Liver Neoplasms* / therapy
  • Male
  • Middle Aged
  • Neoplasm Proteins* / blood
  • Neoplasm Proteins* / immunology
  • Survival Rate
  • alpha-Fetoproteins* / immunology
  • alpha-Fetoproteins* / metabolism

Substances

  • AFP protein, human
  • ICAM1 protein, human
  • Neoplasm Proteins
  • alpha-Fetoproteins
  • Intercellular Adhesion Molecule-1

Grants and funding

This work was supported by National Natural Science Foundation of China, No. 81672753.