Bosutinib Inhibits EGFR Activation in Head and Neck Cancer.

Int J Mol Sci

Molecular Oncology Unit, CIEMAT (ed 70A), Ave Complutense 40, 28040 Madrid, Spain.

Published: June 2018

AI Article Synopsis

  • Head and neck squamous cell carcinoma (HNSCC) is a prevalent cancer with poor survival rates, highlighting the need for effective treatments.
  • Bosutinib, a drug used for leukemia, has shown promise in reducing cell growth and inducing cell death in HNSCC cell lines.
  • The effectiveness of Bosutinib is linked to EGFR activity and may work even better when combined with Alpelisib, especially in cases with specific genetic mutations.

Article Abstract

Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer worldwide, and although new therapeutic approaches have been recently evaluated, overall patient survival is still poor. Thus, new effective and selective clinical treatments are urgently needed. An analysis of data from large-scale, high-throughput drug screening cell line projects identified Bosutinib, a Src/Abl inhibitor that is currently used for the treatment of chronic myelogenous leukemia, as a candidate drug to treat HNSCC. Using a panel of HNSCC-derived cell lines, we found that treatment with Bosutinib reduced cell proliferation and induced apoptosis of sensitive cell lines. The drug rapidly inhibited Src and EGFR (epidermal growth factor receptor) phosphorylation, and sensitivity to Bosutinib was correlated with the activation status of EGFR. Similar findings were observed in in vivo xenograft assays using HNSCC derived cells. Moreover, in the presence of mutations in , the combination of Bosutinib with the PI3Kα inhibitor Alpelisib showed a synergistic effect. These results suggest that Bosutinib could be a new effective drug for the treatment of HNSCC, particularly in tumors with high EGFR activity. Its combination with Alpelisib could especially benefit patients bearing activating mutations of .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073167PMC
http://dx.doi.org/10.3390/ijms19071824DOI Listing

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