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Gastric cancer is one of the most common malignancies and a leading cause of cancer death worldwide. The prognosis of stomach cancer is generally poor as this cancer is not very sensitive to commonly used chemotherapies. Epigenetic modifications play a key role in gastric cancer and contribute to the development and progression of this malignancy. In order to explore new treatment options in this target area we have screened a library of epigenetic inhibitors against gastric cancer cell lines and identified inhibitors for the BET family of bromodomains as potent inhibitors of gastric cancer cell proliferations. Here we show that both the pan-BET inhibitor (+)-JQ1 as well as a newly developed specific isoxazole inhibitor, PNZ5, showed potent inhibition of gastric cancer cell growth. Intriguingly, we found differences in the antiproliferative response between gastric cancer cells tested derived from Brazilian patients as compared to those from Asian patients, the latter being largely resistant to BET inhibition. As BET inhibitors are entering clinical trials these findings provide the first starting point for future therapies targeting gastric cancer.

Original publication

DOI

10.18632/oncotarget.9766

Type

Journal article

Journal

Oncotarget

Publication Date

12/07/2016

Volume

7

Pages

43997 - 44012

Keywords

BET inhibitors, bromodomain, cytotoxicity, epigenetic, gastric cancer, Apoptosis, Asian Continental Ancestry Group, Azepines, Brazil, Cell Cycle Proteins, Cell Line, Tumor, Cell Proliferation, Gene Expression Profiling, HEK293 Cells, Humans, Isoxazoles, Molecular Structure, Nuclear Proteins, Proto-Oncogene Proteins c-myc, Spheroids, Cellular, Stomach Neoplasms, Transcription Factors, Triazoles