Abstract

Brahma related gene product 1 (BRG1) is an ATPase that drives the catalytic activity of a subset of the mammalian SWI/SNF chromatin remodeling enzymes. BRG1 is overexpressed in most human breast cancer tumors without evidence of mutation and is required for breast cancer cell proliferation. We demonstrate that knockdown of BRG1 sensitized triple negative breast cancer cells to chemotherapeutic drugs used to treat breast cancer. An inhibitor of the BRG1 bromodomain had no effect on breast cancer cell viability, but an inhibitory molecule that targets the BRG1 ATPase activity recapitulated the increased drug efficacy observed in the presence of BRG1 knockdown. We further demonstrate that inhibition of BRG1 ATPase activity blocks the induction of ABC transporter genes by these chemotherapeutic drugs and that BRG1 binds to ABC transporter gene promoters. This inhibition increased intracellular concentrations of the drugs, providing a likely mechanism for the increased chemosensitivity. Since ABC transporters and their induction by chemotherapy drugs are a major cause of chemoresistance and treatment failure, these results support the idea that targeting the enzymatic activity of BRG1 would be an effective adjuvant therapy for breast cancer.

Highlights

  • Drugs that target genomically defined vulnerabilities in human tumors have been effective cancer therapies for decades [1]

  • We further demonstrate that inhibition of Brahma related gene product 1 (BRG1) ATPase activity blocks the induction of ATP-binding cassette (ABC) transporter genes by these chemotherapeutic drugs and that BRG1 binds to ABC transporter gene promoters

  • Previous work by us and others indicates that BRG1 is overexpressed in most breast tumors regardless of classification and that BRG1 knockdown in triple negative breast cancer cells caused a slow proliferation phenotype [27, 33]

Read more

Summary

Introduction

Drugs that target genomically defined vulnerabilities in human tumors have been effective cancer therapies for decades [1]. The rapid acquisition of resistance to drug treatments remains a substantial challenge to the clinical management of advanced cancers. Resistance to single drugs can be overcome by combinatorial treatment with drugs acting via different mechanisms, but cancer cells often evolve simultaneous resistance to different structurally and functionally unrelated drugs, a phenomenon known as multidrug resistance (MDR) [7, 8]. Resistance to anticancer drugs arises by various mechanisms and especially by the genetic instability of tumor cells driving heterogeneity. While therapies have become more targeted and effective, acquired resistance has remained the principal basis for treatment failure [9, 10]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call