组蛋白乙酰转移酶
乙酰化
雌激素受体
乳腺癌
基因敲除
癌症研究
化学
雌激素受体α
生物
癌症
生物化学
基因
遗传学
作者
Somya Ranjan Dash,Chinmay Das,Biswajit Das,Atala Bihari Jena,Subarno Paul,Saptarshi Sinha,Jasaswini Tripathy,Chanakya Nath Kundu
出处
期刊:Nanomedicine
日期:2024-01-31
卷期号:19 (7): 581-596
标识
DOI:10.2217/nnm-2023-0269
摘要
Aim: This study aimed to determine if quinacrine–gold hybrid nanoparticles (QAuNPs) + near-infrared (NIR) deregulate HSP-70/P300 complex-mediated H3K14 acetylation in estrogen receptor/progesterone receptor (ER/PR+) breast cancer stem cells (CSCs). Materials & methods: Various cells and mouse-based systems were used as models. Results: QAuNP + NIR treatment reduced the nuclear translocation of HSP-70, affected the histone acetyltransferase activity of P300 and specifically decreased H3K14 acetylation in ER/PR+ breast CSCs. Finally, HSP-70 knockdown showed a reduction in P300 histone acetyltransferase activity, decreased H3K14 acetylation and inhibited activation of the TGF-β gene. Conclusion: This study revealed that QAuNP + NIR irradiation inhibits oncogenic activation of the TGF-β gene by decreasing H3K14 acetylation mediated through the HSP-70/P300 nuclear complex in ER/PR+ breast CSCs.
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