上睑下垂
程序性细胞死亡
癌症研究
免疫原性细胞死亡
转移
免疫系统
血管生成
肿瘤微环境
免疫疗法
癌细胞
乳腺癌
细胞凋亡
癌症
生物
免疫学
医学
内科学
生物化学
作者
Chunlian Zhong,Yumei Li,Wulin Li,Shu Lian,Ye Li,Changhui Wu,Kun Zhang,Guiyu Zhou,Weiyu Wang,Huo Xu,Mingqing Huang,Vladimir L. Katanaev,Lee Jia,Yusheng Lu
标识
DOI:10.1016/j.fct.2023.113654
摘要
Regulation of tumor cell death is a fundamental mechanism for tumor treatment. However, most tumors are resistant to cell death. Triggering inflammatory cell death, pyroptosis, may provide a new view of enhancing tumor cell death. Here we report a new role of Ganoderma lucidum extract (GLE) in pyroptotic cell death. Treatment with GLE (50–200 μg/mL) significantly elevated reactive oxygen species (ROS) levels and caused pyroptotic cell death in breast cancer cells. Mechanistically, GLE activates caspase 3 and further cleaves the gasdermin E (GSDME) protein to form pores on the cell membrane, releasing massive amounts of inflammatory factors in breast cancer cells. We also showed that GLE enhanced antitumor immune responses by substantially increasing the subsets of natural killer (NK) and CD8+T cells in the peripheral immune system and tumor microenvironment. In addition, GLE destroys multiple steps of tumor metastasis, including adhesion, migration, invasion, colonization, and angiogenesis. Collectively, these results suggest that GLE provides a potential approach for breast cancer treatment, which may complement chemotherapy or immunotherapy for cancer metastasis.
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