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Functional Regulation of Ginsenosides on Myeloid Immunosuppressive Cells in the Tumor Microenvironment
Yanfei Zhang1, Zhidong Qiu1, Ye Qiu2
1Changchun University of Chinese Medicine, Changchun, Jilin, People's Republic of China.
Abstract:
Ginsenosides, the key components isolated from ginseng, have been extensively studied in antitumor treatment. Numerous studies have shown that ginsenosides have direct function in tumor cells through the induction of cancer cell apoptosis and the inhibition of cancer cell growth and enhance the antitumor immunity through the activation of cytotoxic T lymphocytes and natural killer cells. However, little is known about the function of ginsenosides on myeloid immunosuppressive cells including dendritic cells in tumor, tumor-associated macrophages, and myeloid-derived suppressor cells in the tumor microenvironments. Those myeloid immunosuppressive cells play important roles in promoting tumor angiogenesis, invasion, and metastasis. In the review, we summarize the regulatory functions of ginsenosides on myeloid immunosuppressive cells in tumor microenvironment, providing the novel therapeutic methods for clinical cancer treatment.
Insights
Ginsenosides from ginseng show promise in cancer treatment by targeting tumor cells and boosting immune responses. This review explores their role in modulating myeloid immunosuppressive cells within the tumor microenvironment for novel cancer therapies.
Area of Science:
- Natural Products Chemistry
- Immunology
- Cancer Biology
Background:
- Ginsenosides, derived from ginseng, are recognized for their antitumor properties.
- Existing research highlights their direct effects on cancer cells, including apoptosis induction and growth inhibition.
- Their impact on enhancing anti-tumor immunity via T lymphocytes and natural killer cells is also documented.
Purpose of the Study:
- To investigate the less-understood functions of ginsenosides on myeloid immunosuppressive cells.
- To explore the role of ginsenosides in modulating dendritic cells, tumor-associated macrophages, and myeloid-derived suppressor cells.
- To provide insights into novel therapeutic strategies for cancer treatment by targeting these myeloid cells.
Main Methods:
- Literature review of existing studies on ginsenosides and myeloid cells in the tumor microenvironment.
- Analysis of research detailing the regulatory functions of ginsenosides on immunosuppressive myeloid cell populations.
- Synthesis of information on how ginsenosides influence angiogenesis, invasion, and metastasis via these cells.
Main Results:
- Ginsenosides exhibit regulatory effects on various myeloid immunosuppressive cells within the tumor microenvironment.
- These compounds influence key processes such as tumor angiogenesis, invasion, and metastasis.
- Understanding these interactions opens avenues for ginsenoside-based cancer therapies.
Conclusions:
- Ginsenosides represent a potential therapeutic agent for modulating the tumor microenvironment.
- Targeting myeloid immunosuppressive cells with ginsenosides offers a novel approach to cancer treatment.
- Further research into ginsenoside mechanisms can lead to improved clinical outcomes in oncology.
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