Dihydrotanshinone I potentiates the anti-tumor activity of cisplatin by activating ROS-mediated ER stress through targeting HSPD1 in lung cancer cells.

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Tác giả: Liyuan Cheng, Ri Cui, Haizhen Lin, Yiwei Shen, Hehuan Sui, Jiaying Wang, Chenjun Xie, Congying Xie, Ying Yu, Yun Yu

Ngôn ngữ: eng

Ký hiệu phân loại: 949.59012 *Greece

Thông tin xuất bản: Netherlands : European journal of pharmacology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 465128

Lung cancer represents one of the most lethal malignancies, characterized by the highest incidence and mortality rates globally. Cisplatin-based chemotherapy exerts powerful anti-tumor activities in lung cancer, whereas its clinical application was limited due to the severe side effects. Dihydrotanshinone I (DHTS), a root extract from Salvia miltiorrhiza, exhibits diverse biological functions, encompassing liver protection, anti-inflammatory properties, promotion of osteoclast differentiation, and induction of apoptosis in tumor cells. DHTS exerts anti-tumor effects in various cancers, however, its biological functions in lung cancer are largely unknown. We demonstrated that DHTS synergistically increased the tumor suppressive effects of cisplatin in lung cancer cells by activating reactive oxygen species (ROS)-mediated endoplasmic reticulum stress (ER stress) and c-Jun N-terminal kinase (JNK) signaling pathways, both in vitro and in vivo. Additionally, DHTS induced excessive ROS accumulation by inhibiting the expression of Heat Shock Proteins 60 (HSPD1). Silencing HSPD1 augmented the anti-tumor effects of DHTS in lung cancer cells, primarily through the stimulation of ROS-mediated ER stress and JNK pathways. Our study suggests that DHTS possesses druggable potential, and combined therapy with DHTS and cisplatin may be a promising therapeutic strategy for certain lung cancer patients.
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