FERREG: ferroptosis-based regulation of disease occurrence, progression and therapeutic response

  • 0Key Laboratory of Elemene Class Anti-Cancer Chinese Medicines, Engineering Laboratory of Development and Application of Traditional Chinese Medicines, Collaborative Innovation Center of Traditional Chinese Medicines of Zhejiang Province, School of Pharmacy, and Department of Respiratory Medicine of Affiliated Hospital, Hangzhou Normal University, Hangzhou, 311121, China.

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Summary

This summary is machine-generated.

Ferroptosis, a cell death form linked to diseases, is detailed in the new FERREG database. This resource maps ferroptosis regulators, drugs, and disease links, aiding research and potential treatments.

Area Of Science

  • Biochemistry and Molecular Biology
  • Cell Biology
  • Genetics

Background

  • Ferroptosis is an iron-dependent cell death pathway implicated in diseases like cancer and neurodegeneration.
  • Its regulation involves key pathways: system Xc-/GPX4 axis, lipid peroxidation, and iron metabolism.
  • Understanding ferroptosis mechanisms is crucial for developing new therapeutic strategies.

Purpose Of The Study

  • To introduce FERREG, a novel database for ferroptosis-related information.
  • To consolidate data on ferroptosis regulation, disease association, and drug responses.
  • To provide a comprehensive resource for researchers investigating ferroptosis.

Main Methods

  • Systematic literature review and data mining.
  • Integration of data from existing biological databases.
  • Curation of information on ferroptosis targets, regulators, drugs, and disease associations.

Main Results

  • The FERREG database contains 51 targets, 718 regulators, 445 drugs, and 158 disease responses related to ferroptosis.
  • It explicitly describes molecular mechanisms and references data through cross-linking.
  • FERREG provides a centralized platform for accessing ferroptosis-related knowledge.

Conclusions

  • FERREG serves as a valuable, comprehensive resource for the ferroptosis research community.
  • The database facilitates understanding of ferroptosis's role in disease and drug development.
  • It supports the exploration of novel therapeutic interventions targeting ferroptosis.

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