Astragalus Polysaccharide (PG2) Suppresses Macrophage Migration Inhibitory Factor and Aggressiveness of Lung Adenocarcinoma Cells

Author:

Liao Chien-Huang1,Yong Chen-Yin2,Lai Gi-Ming13456,Chow Jyh-Ming34,Cheng Chieh-Fang7,Fang Chia-Lang8,Lin Pei-Chun1,Chang Chia-Lun34,Zheng Yu-Mei3,Chuang Shuang-En6,Whang-Peng Jacqueline135,Yao Chih-Jung14

Affiliation:

1. Cancer Center, Wan Fang Hospital, Taipei Medical University, Taipei 11696, Taiwan

2. Division of Oral and Maxillofacial Surgery, Department of Dentistry, Wan Fang Hospital, Taipei Medical University, Taipei 11696, Taiwan

3. Division of Hematology and Medical Oncology, Department of Internal Medicine, Wan Fang Hospital, Taipei Medical University, Taipei 11696, Taiwan

4. Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei 11031, Taiwan

5. Taipei Cancer Center, Taipei Medical University, Taipei 11031, Taiwan

6. National Institute of Cancer Research, National Health Research Institutes, Miaoli 35053, Taiwan

7. PhytoHealth Corporation, Taipei 10547, Taiwan

8. Department of Pathology, Wan Fang Hospital, Taipei Medical University, Taipei 11696, Taiwan

Abstract

Astragalus membranaceus is the most popular traditional Chinese medicine for managing vital energy deficiency. Its injectable polysaccharide PG2 has been used for relieving cancer-related fatigue, and PG2 has immune-modulatory and anti-inflammatory effects. In this study, we explored the effects of PG2 in lung adenocarcinoma A549 and CL1-2 cells and investigated its anticancer activity, and the results were validated in severe combined immunodeficiency (SCID) mice. Although PG2 did not inhibit the growth of these cells, it dose-dependently suppressed their migration and invasion, accompanied by reduced vimentin and AXL and induced epithelial cadherin (E-cadherin) expression. Regarding the underlying molecular mechanism, PG2 treatment reduced the macrophage migration inhibitory factor (MIF), an inflammatory cytokine that promotes the epithelial–mesenchymal transition and aggressiveness of cancer cells. Consistent with the previous finding that MIF regulates matrix metalloproteinase-13 (MMP-13) and AMP-activated protein kinase (AMPK), treatment with PG2 reduced MMP-13 and activated AMPK in A549 and CL1-2 cells in this study. In SCID mice injected with A549 cells through the tail vein, intraperitoneal injection with PG2 reduced lung and abdominal metastases in parallel with decreased immunohistochemical staining of AXL, vimentin, MMP-13, and MIF in the tumor. Collectively, data revealed a potential application of PG2 in integrative cancer treatment through the suppression of MIF in cancer cells and their aggressiveness.

Funder

Wan Fang Hospital, Taipei Medical University, and PhytoHealth Corporation, Taipei, Taiwan

Health and Welfare Surcharge of tobacco products

Ministry of Science and Technology, Taiwan

Publisher

World Scientific Pub Co Pte Lt

Subject

Complementary and alternative medicine,General Medicine

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