TY - JOUR
T1 - Ganoderma lucidum extract promotes tumor cell pyroptosis and inhibits metastasis in breast cancer
AU - Zhong, Chunlian
AU - Li, Yumei
AU - Li, Wulin
AU - lian, Shu
AU - Li, Ye
AU - Wu, Changhui
AU - Zhang, Kun
AU - Zhou, Guiyu
AU - Wang, Weiyu
AU - Xu, Huo
AU - Huang, Mingqing
AU - Katanaev, Vladimir
AU - Jia, Lee
AU - Lu, Yusheng
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/4
Y1 - 2023/4
N2 - 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.
AB - 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.
KW - Cytotoxic lymphocytes
KW - Ganoderma lucidum extract
KW - Gasdermin E
KW - Pyroptotic cell death
KW - Tumor metastasis
UR - https://www.scopus.com/pages/publications/85150079377
U2 - 10.1016/j.fct.2023.113654
DO - 10.1016/j.fct.2023.113654
M3 - Article
C2 - 36758785
AN - SCOPUS:85150079377
SN - 0278-6915
VL - 174
JO - Food and Chemical Toxicology
JF - Food and Chemical Toxicology
M1 - 113654
ER -