| Literature DB >> 30450651 |
Xiao-Han Jin1,2,3, Yong-Sheng Jia1,2,3, Ye-Hui Shi1,2,3, Qiu-Ying Li4,5, Shi-Qi Bao6, Wen-Ping Lu7, Zhong-Sheng Tong1,2,3.
Abstract
Endocrine therapy is one of the main treatments for estrogen receptor-positive breast cancers. Tamoxifen is the most commonly used drug for endocrine therapy. However, primary or acquired tamoxifen resistance occurs in a large proportion of breast cancer patients, leading to therapeutic failure. We found that the combination of tamoxifen and ACT001, a nuclear factor-κB (NF-κB) signaling pathway inhibitor, effectively inhibited the proliferation of both tamoxifen-sensitive and tamoxifen-resistant cells. The tamoxifen-resistant cell line MCF7R/LCC9 showed active NF-κB signaling and high apoptosis-related gene transcription, especially for antiapoptotic genes, which could be diminished by treatment with ACT001. These results demonstrate that ACT001 can prevent and reverse tamoxifen resistance by inhibiting NF-κB activation.Entities:
Keywords: ACT001; apoptosis; breast neoplasms; endocrine therapy; nuclear factor-κB; tamoxifen resistance
Year: 2018 PMID: 30450651 DOI: 10.1002/jcb.27146
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429