阿霉素
三阴性乳腺癌
伏立诺他
癌症研究
组蛋白脱乙酰酶抑制剂
体内
组蛋白脱乙酰基酶
乳腺癌
癌症
癌细胞
背景(考古学)
化学
药理学
转移
细胞生长
HDAC1型
医学
化疗
生物
内科学
组蛋白
生物化学
古生物学
生物技术
基因
作者
Yuheng Pang,Runze Shi,Liujia Chan,Lu Yu,Di Zhu,Tong Liu,Meisi Yan,Yuji Wang,Wenjing Wang
标识
DOI:10.1016/j.phrs.2023.106926
摘要
Vorinostat (SAHA) is a histone deacetylase inhibitor that exerts its effects through epigenetic regulation. Specifically, SAHA can inhibit the proliferation of triple-negative breast cancer (TNBC) cells alone or in combination with other chemotherapeutic agents. Doxorubicin (DOX), a traditional chemotherapeutic drug, exhibits a potent cytotoxic effect on cancer cells while also inducing strong toxic effects. In this study, we investigated the synergistic potential of these two drugs in combination against TNBC. Our results suggested that the combination of these two drugs could enhance the inhibitory effect on cancer cell proliferation, resulting in alterations in cell mitotic phase, and suppression of cancer cell stemness. Moreover, our in vivo study unveiled that when SAHA was combined with DOX, it not only exhibited an inhibitory effect on tumor metastasis but also played a role in regulating the immune microenvironment within tumors. Overall, the combination of DOX and SAHA presents a promising avenue for innovative combination chemotherapy in the context of TNBC.
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