| Literature DB >> 29396630 |
Alexandra Canonici1, Zulfiqar Qadir1, Neil T Conlon1, Denis M Collins1, Neil A O'Brien2, Naomi Walsh1, Alex J Eustace3, Norma O'Donovan1, John Crown1,4.
Abstract
As HER2 is a client protein of the molecular chaperone Hsp90, targeting Hsp90 may be beneficial in HER2-positive breast cancer. In this study, the activity of the Hsp90 inhibitor NVP-AUY922 was assessed in HER2 overexpressing breast cancer cell lines, including two cell line models of acquired trastuzumab-resistance. The seven HER2-positive breast cancer cell lines tested showed significant sensitivity to NVP-AUY922 in vitro, with IC50 values between 6 and 17 nM. Combining NVP-AUY922 with chemotherapy did not improve response. NVP-AUY922 in combination with trastuzumab, significantly enhanced growth inhibition in three of the seven cell lines tested. In conclusion, our data shows that NVP-AUY922 displays potent anti-cancer activity in HER2-positive and trastuzumab-resistant breast cancer cells, and supports further testing of NVP-AUY922 in patients with HER2-positive breast cancer.Entities:
Keywords: AUY922; ErbB2; Hsp90 (heat shock protein 90); Trastuzumab
Mesh:
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Year: 2018 PMID: 29396630 DOI: 10.1007/s10637-017-0556-7
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850