Betulinic Acid Inhibits the Stemness of Gastric Cancer Cells by Regulating the GRP78-TGF-β1 Signaling Pathway and Macrophage Polarization

Author:

Chen Jen-Lung1ORCID,Tai Yun-Shen2,Tsai Hsin-Yi34,Hsieh Chia-Yuan3,Chen Chun-Lin5ORCID,Liu Chung-Jung67ORCID,Wu Deng-Chyang67,Huang Yaw-Bin38ORCID,Lin Ming-Wei479ORCID

Affiliation:

1. Department of Surgery, E-Da Hospital, Kaohsiung 82445, Taiwan

2. Department of Surgery, China Medical University, An-Nan Hospital, Tainan 70965, Taiwan

3. School of Pharmacy, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

4. Department of Medical Research, E-Da Hospital/E-Da Cancer Hospital, Kaohsiung 82445, Taiwan

5. Department of Biological Science, National Sun Yat-sen University, Kaohsiung 80424, Taiwan

6. Division of Gastroenterology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan

7. Regenerative Medicine and Cell Therapy Research Center, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

8. Center for Cancer Research, Kaohsiung Medical University, Kaohsiung 80708, Taiwan

9. Department of Nursing, College of Medicine, I-Shou University, Kaohsiung 82445, Taiwan

Abstract

Cancer stemness is the process by which cancer cells acquire chemoresistance and self-renewal in the tumor microenvironment. Glucose-regulated protein 78 (GRP78) is a biomarker for gastric cancer and is involved in cancer stemness. By inducing cancer stemness in various types of cancer, the polarization of macrophages into tumor-associated macrophages (TAMs) controls tumor progression. Betulinic acid (BA) is a bioactive natural compound with anticancer properties. However, whether GRP78 regulates TAM-mediated cancer stemness in the tumor microenvironment and whether BA inhibits GRP78-mediated cancer stemness in gastric cancer remain unknown. In this study, we investigated the role of GRP78 in gastric cancer stemness in a tumor microenvironment regulated by BA. The results indicated that BA inhibited not only GRP78-mediated stemness-related protein expression and GRP78-TGF-β-mediated macrophage polarization into TAMs, but also TAM-mediated cancer stemness. Therefore, BA is a promising candidate for clinical application in combination-chemotherapy targeting cancer stemness.

Funder

Ministry of Science and Technology

E-Da Hospital

An-Nan Hospital

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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