Anti-tumor effect of flavonoids isolated from Bidens Pilosa L. by regulating the activity of myeloid-derived suppressor cells within the tumor microenvironment in mice.
[ETHNOPHARMACOLOGICAL RELEVANCE] Colon cancer is one of the most common malignant tumors worldwide.
APA
Tao Y, Du M, et al. (2026). Anti-tumor effect of flavonoids isolated from Bidens Pilosa L. by regulating the activity of myeloid-derived suppressor cells within the tumor microenvironment in mice.. Journal of ethnopharmacology, 355(Pt A), 120635. https://doi.org/10.1016/j.jep.2025.120635
MLA
Tao Y, et al.. "Anti-tumor effect of flavonoids isolated from Bidens Pilosa L. by regulating the activity of myeloid-derived suppressor cells within the tumor microenvironment in mice.." Journal of ethnopharmacology, vol. 355, no. Pt A, 2026, pp. 120635.
PMID
40998135
Abstract
[ETHNOPHARMACOLOGICAL RELEVANCE] Colon cancer is one of the most common malignant tumors worldwide. Bidens pilosa L., an annual herb of the Asteraceae, has long been used to treat inflammatory-related illnesses, including cancer. As a population of immunosuppressive cells in the TME, MDSCs play a pivotal role in tumorigenesis and progression, and the effect of B. pilosa on MDSCs has rarely been reported.
[AIM OF STUDY] To investigate the anti-tumor effect of a mixture of two flavonoids, MTF, isolated from B. pilosa, which showed immunotherapeutic activity in regulating the function of MDSCs in colon cancer.
[MATERIALS AND METHODS] The regulatory effects of the flavonoid MTF on MDSCs differentiation and immune function were tested by qRT-PCR and flow cytometry. Its underlying immunotherapeutic mechanism, cytotoxicity, and anti-angiogenic activity were investigated using SIE luciferase/Western blot, CCK-8/apoptosis, and MDSC-HUVEC co-culture assays, respectively. The in vivo anti-tumor activity of MTF was subsequently investigated in both CT26. WT and CT26. WT/MDSCs syngeneic models.
[RESULTS] MTF and its components effectively depleted MDSCs by inhibiting their differentiation and inducing apoptosis, thereby restoring suppressed CD4 T cell function. In vivo, MTF not only reduced intratumoral MDSCs but also counteracted MDSC-driven angiogenesis, leading to inhibited tumor growth and enhanced sensitivity to 5-FU treatment.
[CONCLUSION] Flavonoid MTF showed a good anti-tumor effect in mice by regulating MDSCs activity within the TME, which contributes to the clinical use of this traditional herb.
[AIM OF STUDY] To investigate the anti-tumor effect of a mixture of two flavonoids, MTF, isolated from B. pilosa, which showed immunotherapeutic activity in regulating the function of MDSCs in colon cancer.
[MATERIALS AND METHODS] The regulatory effects of the flavonoid MTF on MDSCs differentiation and immune function were tested by qRT-PCR and flow cytometry. Its underlying immunotherapeutic mechanism, cytotoxicity, and anti-angiogenic activity were investigated using SIE luciferase/Western blot, CCK-8/apoptosis, and MDSC-HUVEC co-culture assays, respectively. The in vivo anti-tumor activity of MTF was subsequently investigated in both CT26. WT and CT26. WT/MDSCs syngeneic models.
[RESULTS] MTF and its components effectively depleted MDSCs by inhibiting their differentiation and inducing apoptosis, thereby restoring suppressed CD4 T cell function. In vivo, MTF not only reduced intratumoral MDSCs but also counteracted MDSC-driven angiogenesis, leading to inhibited tumor growth and enhanced sensitivity to 5-FU treatment.
[CONCLUSION] Flavonoid MTF showed a good anti-tumor effect in mice by regulating MDSCs activity within the TME, which contributes to the clinical use of this traditional herb.
MeSH Terms
Animals; Bidens; Myeloid-Derived Suppressor Cells; Flavonoids; Tumor Microenvironment; Mice; Antineoplastic Agents, Phytogenic; Mice, Inbred BALB C; Cell Line, Tumor; Colonic Neoplasms; Humans; Apoptosis; Cell Differentiation; Male; Female
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