Ze-Qi-Tang Formula Induces Granulocytic Myeloid-Derived Suppressor Cell Apoptosis via STAT3/S100A9/Bcl-2/Caspase-3 Signaling to Prolong the Survival of Mice with Orthotopic Lung Cancer

Author:

Xu Zi-hang1,Zhu Yang-zhuangzhuang1ORCID,Su Lin1ORCID,Tang Xue-yang2,Yao Chao1,Jiao Xiao-ning1ORCID,Hou Yi-fei1ORCID,Chen Xiao1,Wei Lu-yao1,Wang Wan-tao1,Wang Jie1,Gong Chen-yuan1,Zhu Xian-dan3,Zhang Fei4ORCID,Zhu Shi-guo1ORCID,Zou Chun-pu1ORCID

Affiliation:

1. School of Basic Medical Science, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China

2. School of Chinese Medicine, Hunan University of Chinese Medicine, Changsha 410208, China

3. Center of Technology Experiment, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China

4. Department of General Surgery, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University, School of Medicine, Shanghai 200092, China

Abstract

Non-small-cell lung cancer (NSCLC) remains the most common malignancy with the highest morbidity and mortality worldwide. In our previous study, we found that a classic traditional Chinese medicine (TCM) formula Ze-Qi-Tang (ZQT), which has been used in the treatment of respiratory diseases for thousands of years, could directly inhibit the growth of human NSCLC cells via the p53 signaling pathway. In this study, we explored the immunomodulatory functions of ZQT. We found that ZQT significantly prolonged the survival of orthotopic lung cancer model mice by modulating the tumor microenvironment (TME). ZQT remarkably reduced the number of MDSCs (especially G-MDSCs) and inhibited their immunosuppressive activity by inducing apoptosis in these cells via the STAT3/S100A9/Bcl-2/caspase-3 signaling pathway. When G-MDSCs were depleted, the survival promotion effect of ZQT and its inhibitory effect on lung luminescence signal disappeared in tumor-bearing mice. This is the first study to illustrate the immunomodulatory effect of ZQT in NSCLC and the underlying molecular mechanism.

Funder

Shanghai Committee of Science and Technology

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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