EZH2-mediated PP2A inactivation confers resistance to HER2-targeted breast cancer therapy.

Abstract:

:HER2-targeted therapy has yielded a significant clinical benefit in patients with HER2+ breast cancer, yet disease relapse due to intrinsic or acquired resistance remains a significant challenge in the clinic. Here, we show that the protein phosphatase 2A (PP2A) regulatory subunit PPP2R2B is a crucial determinant of anti-HER2 response. PPP2R2B is downregulated in a substantial subset of HER2+ breast cancers, which correlates with poor clinical outcome and resistance to HER2-targeted therapies. EZH2-mediated histone modification accounts for the PPP2R2B downregulation, resulting in sustained phosphorylation of PP2A targets p70S6K and 4EBP1 which leads to resistance to inhibition by anti-HER2 treatments. Genetic depletion or inhibition of EZH2 by a clinically-available EZH2 inhibitor restores PPP2R2B expression, abolishes the residual phosphorylation of p70S6K and 4EBP1, and resensitizes HER2+ breast cancer cells to anti-HER2 treatments both in vitro and in vivo. Furthermore, the same epigenetic mechanism also contributes to the development of acquired resistance through clonal selection. These findings identify EZH2-dependent PPP2R2B suppression as an epigenetic control of anti-HER2 resistance, potentially providing an opportunity to mitigate anti-HER2 resistance with EZH2 inhibitors.

journal_name

Nat Commun

journal_title

Nature communications

authors

Bao Y,Oguz G,Lee WC,Lee PL,Ghosh K,Li J,Wang P,Lobie PE,Ehmsen S,Ditzel HJ,Wong A,Tan EY,Lee SC,Yu Q

doi

10.1038/s41467-020-19704-x

subject

Has Abstract

pub_date

2020-11-18 00:00:00

pages

5878

issue

1

issn

2041-1723

pii

10.1038/s41467-020-19704-x

journal_volume

11

pub_type

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