Mismatch repair deficiency predicts response to HER2 blockade in HER2-negative breast cancer.

ABSTRACT: Resistance to endocrine treatment occurs in ~30% of ER⁺ breast cancer patients resulting in ~40,000 deaths/year in the USA. Preclinical studies strongly implicate activation of growth factor receptor, HER2 in endocrine treatment resistance. However, clinical trials of pan-HER inhibitors in ER⁺/HER2^- patients have disappointed, likely due to a lack of predictive biomarkers. Here we demonstrate that loss of mismatch repair activates HER2 after endocrine treatment in ER⁺/HER2^- breast cancer cells by protecting HER2 from protein trafficking. Additionally, HER2 activation is indispensable for endocrine treatment resistance in MutL^- cells. Consequently, inhibiting HER2 restores sensitivity to endocrine treatment. Patient data from

SUBMITTER: Punturi NB 

PROVIDER: S-EPMC8134423 | biostudies-literature | 2021 May

REPOSITORIES: biostudies-literature