AI Article Synopsis

  • Metastasis is a critical stage in cancer progression, causing over 90% of cancer-related deaths, and understanding its cellular mechanisms is essential for research.
  • The MET network visualization tool was developed to help researchers analyze relationships among genes, cancers, and tissues in PubMed studies using text-mining techniques.
  • As a browser extension, MET allows curators to edit and review metastatic information directly in PubMed and facilitated the curation of 963 unique metastatic relations in a 2015 interactive task.

Article Abstract

Metastasis is the dissemination of a cancer/tumor from one organ to another, and it is the most dangerous stage during cancer progression, causing more than 90% of cancer deaths. Improving the understanding of the complicated cellular mechanisms underlying metastasis requires investigations of the signaling pathways. To this end, we developed a METastasis (MET) network visualization and curation tool to assist metastasis researchers retrieve network information of interest while browsing through the large volume of studies in PubMed. MET can recognize relations among genes, cancers, tissues and organs of metastasis mentioned in the literature through text-mining techniques, and then produce a visualization of all mined relations in a metastasis network. To facilitate the curation process, MET is developed as a browser extension that allows curators to review and edit concepts and relations related to metastasis directly in PubMed. PubMed users can also view the metastatic networks integrated from the large collection of research papers directly through MET. For the BioCreative 2015 interactive track (IAT), a curation task was proposed to curate metastatic networks among PubMed abstracts. Six curators participated in the proposed task and a post-IAT task, curating 963 unique metastatic relations from 174 PubMed abstracts using MET.Database URL: http://btm.tmu.edu.tw/metastasisway.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885604PMC
http://dx.doi.org/10.1093/database/baw090DOI Listing

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