AI Article Synopsis

  • Non-small cell lung cancer (NSCLC) is the most common type of lung cancer, responsible for a significant number of cancer deaths worldwide (80%-85% of lung cancers).
  • Targeting the Ras/Raf/MEK/ERK MAPK signaling pathway represents a promising strategy in NSCLC treatment, allowing for the development of targeted therapies.
  • The article emphasizes the potential of repurposing existing non-cancer drugs and integrating them with current therapies to improve outcomes for NSCLC patients and increase cure rates.

Article Abstract

Non-small cell lung cancer (NSCLC) is a prominent subtype of lung carcinoma that accounts for the majority of cancer-related deaths globally, and it is responsible for about 80% to 85% of lung cancers. Mitogen-Activated Protein Kinase (MAPK) signaling pathways are a vital aspect of NSCLC, and have aided in the advancement of therapies for this carcinoma. Targeting the Ras/Raf/MEK/ERK pathway is a promising and alternative method in NSCLC treatment, which is highlighted in this review. The introduction of targeted medicines has revolutionized the treatment of patients with this carcinoma. When combined with current systems biology-driven stratagems, repurposing non-cancer drugs into new therapeutic niches presents a cost-effective and efficient technique with enhancing outcomes for discovering novel pharmacological activity. This article highlights the successful cutting-edge techniques while focusing on NSCLC targeted therapies. The ultimate challenge will be integrating these repurposed drugs into the therapeutic regimen of patients affected with NSCLC to potentially increase lung cancer cure rates.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8526962PMC
http://dx.doi.org/10.3389/fonc.2021.741326DOI Listing

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