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Autophagy Inhibition by Fangji Huangqi Decoction Enhances Tumor Immunogenicity and Potentiates PD-1 Blockade.

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Cancer science 2026 OA Autophagy in Disease and Therapy
Retraction 확인
출처
PubMed DOI OpenAlex 마지막 보강 2026-04-29
OpenAlex 토픽 · Autophagy in Disease and Therapy Cancer Immunotherapy and Biomarkers Andrographolide Research and Applications

Jiang Y, Zeng S, Wang D, Jiang J, Li Z, Li J, Chen D, Zhao X, Ying Z, Deng Y, Cai Q, Mai S, Zheng J, Yang Q, Liu F, Du B, Xiao J, Liu X, Wang K

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Fangji Huangqi Decoction (FJHQ), a traditional Chinese medicine formula derived from "Jin Gui Yao Lue," has been reported to exhibit immunomodulatory and anti-inflammatory effects.

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BibTeX ↓ RIS ↓
APA Yuxiao Jiang, Shiji Zeng, et al. (2026). Autophagy Inhibition by Fangji Huangqi Decoction Enhances Tumor Immunogenicity and Potentiates PD-1 Blockade.. Cancer science. https://doi.org/10.1111/cas.70399
MLA Yuxiao Jiang, et al.. "Autophagy Inhibition by Fangji Huangqi Decoction Enhances Tumor Immunogenicity and Potentiates PD-1 Blockade.." Cancer science, 2026.
PMID 42015731
DOI 10.1111/cas.70399

Abstract

Fangji Huangqi Decoction (FJHQ), a traditional Chinese medicine formula derived from "Jin Gui Yao Lue," has been reported to exhibit immunomodulatory and anti-inflammatory effects. This study investigates its potential anti-tumor mechanism via the enhancement of CD8 T cell-mediated immunity. In murine B16 melanoma and Lewis lung carcinoma models, FJHQ significantly suppressed tumor growth and enhanced CD8 T cell infiltration and cytotoxicity. CD8 T cell depletion abrogated these effects, confirming their necessity. In vitro, FJHQ treatment augmented antigen presentation by tumor cells through upregulation of MHC-I expression, leading to improved CD8 T cell recognition and killing. Mechanistically, FJHQ inhibited autophagic flux in tumor cells, as evidenced by mCherry-GFP-LC3 reporter assays and electron microscopy, resulting in impaired lysosomal function and elevated MHC-I levels. Furthermore, combining FJHQ with anti-PD-1 therapy synergistically promoted CD8 T cell activity, increased granzyme B and IFN-γ expression, and induced substantial tumor regression. These findings demonstrate that FJHQ enhances antitumor immunity by suppressing autophagy and elevating MHC-I expression, thereby sensitizing tumors to PD-1 blockade. FJHQ represents a promising immunoadjuvant for cancer therapy.

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