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      HER2-L755S mutation induces hyperactive MAPK and PI3K-mTOR signaling, leading to resistance to HER2 tyrosine kinase inhibitor treatment

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          ABSTRACT

          L755S, a HER2 kinase domain mutation, is the most common HER2 mutation in breast cancer associated with resistance to anti-HER2 trastuzumab treatment. Here, we showed that HER2-L755S confers hyperactivation of MAPK and PI3K/AKT/mTOR pathways and resistance to both reversible and irreversible HER2 tyrosine kinase inhibitors. We further demonstrated that the HER2 TKIs in combination with MEK inhibitor, AZD6244, or PI3K inhibitor, GDC0941, yield robust killing in HER2-L755S cancer cells, indicating a novel targeted strategy to overcome HER2-L755S resistance to anti-HER2 treatment.

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          Author and article information

          Journal
          Cell Cycle
          Cell Cycle
          KCCY
          kccy20
          Cell Cycle
          Taylor & Francis
          1538-4101
          1551-4005
          2019
          3 June 2019
          : 18
          : 13
          : 1513-1522
          Affiliations
          [a ] School of Pharmacy, Jinan University , Guangzhou, China
          [b ] Cancer Research Institute, Jinan University , Guangzhou, China
          [c ] Cancer Therapeutics and Stratified Oncology, Genome Institute of Singapore, A*STAR (Agency for Science, Technology and Research) , Biopolis, Singapore
          Author notes
          [*]

          These authors contributed equally to this work.

          Author information
          http://orcid.org/0000-0001-8947-4867
          Article
          PMC6592242 PMC6592242 6592242 1624113
          10.1080/15384101.2019.1624113
          6592242
          31135266
          77ec56eb-ac61-4bda-8551-bada0a35b9df
          © 2019 Informa UK Limited, trading as Taylor & Francis Group
          History
          : 9 April 2019
          : 13 May 2019
          : 14 May 2019
          Page count
          Figures: 5, References: 30, Pages: 10
          Categories
          Research Paper

          combination,neratinib,lapatinib,resistance,L755S,HER2
          combination, neratinib, lapatinib, resistance, L755S, HER2

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