CAFrgDB: a database for cancer-associated fibroblasts related genes and their functions in cancer

Qiang Yuan1, Yi Chu1, Xiaoyu Li1

  • 1Department of Pathophysiology, State Key Laboratory of Esophageal Cancer Prevention and Treatment, School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, 450001, China.

Cancer Gene Therapy
|March 16, 2023
PubMed

Insights

Cancer-associated fibroblasts (CAFs) are key in cancer. This study curated 5421 CAF-related genes (CAFGenes) across 24 cancer types, creating a database (CAFrgDB) for therapeutic target discovery.

Area of Science:

  • Oncology
  • Cancer Biology
  • Bioinformatics

Background:

  • Cancer-associated fibroblasts (CAFs) are crucial components of the tumor microenvironment (TME), influencing cancer progression and serving as therapeutic targets.
  • CAFs exhibit significant heterogeneity and versatility across various cancer types, necessitating specific gene identification for targeted therapies.

Purpose of the Study:

  • To curate and analyze cancer-associated fibroblast-related genes (CAFGenes) across 24 cancer types.
  • To develop a comprehensive database (CAFrgDB) for CAF-related genes and proteins to aid in understanding cancer mechanisms and identifying therapeutic targets.

Main Methods:

  • Collected and curated 5421 CAFGenes from experimental data, categorizing them into responders, secretions, and regulators.
  • Performed gene expression and prognostic marker analyses on human CAFGenes using The Cancer Genome Atlas (TCGA) data.
  • Integrated protein-protein interactions, drug-target relations, and annotations from 9 public databases for CAF-associated proteins.

Main Results:

  • Identified 5421 CAFGenes, including 4982 responders, 1069 secretions, and 281 regulators, spanning 24 cancer types.
  • Conducted gene expression and prognostic analyses, revealing CAFGene roles in cancer.
  • Developed CAFrgDB (http://caf.zbiolab.cn), a publicly accessible resource integrating diverse CAF-related data.

Conclusions:

  • CAFrgDB provides a valuable resource for exploring CAF heterogeneity and identifying novel therapeutic targets in cancer.
  • The curated CAFGenes and integrated annotations facilitate deeper investigation into CAF functions and their impact on cancer pathogenesis.

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