Combination of Anti–PD-1 and Electroacupuncture Induces a Potent Antitumor Immune Response in Microsatellite-Stable Colorectal Cancer

Author:

Wang Yuan123ORCID,Liu Fengyi45ORCID,Du Xiaoxue123ORCID,Shi Jiaqi23ORCID,Yu Rui6ORCID,Li Shuang13ORCID,Na Ruisi123ORCID,Zhao Ying123ORCID,Zhou Meng123ORCID,Guo Ying3ORCID,Cheng Liang7ORCID,Wang Guangyu12ORCID,Zheng Tongsen1238ORCID

Affiliation:

1. 1Department of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, P. R. China.

2. 2Department of Phase 1 Trials Center, Harbin Medical University Cancer Hospital, Harbin, P. R. China.

3. 3Heilongjiang Province Key Laboratory of Molecular Oncology, Harbin, P. R. China.

4. 4Department of Integrated Traditional Chinese and Western Medicine, First Affiliated Hospital of Harbin Medical University, Harbin, P. R. China.

5. 5Heilongjiang University of Chinese Medicine, Harbin, P. R. China.

6. 6College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, P. R. China.

7. 7College of Bioinformatics Science and Technology, NHC Key Laboratory of Molecular Probe and Targeted Diagnosis and Therapy, Harbin Medical University, Harbin, P. R. China.

8. 8Heilongjiang Cancer Institute, Harbin, P. R. China.

Abstract

Abstract Programmed death receptor-1 (PD-1) inhibitors are ineffective against microsatellite-stable (MSS) colorectal cancer. Electroacupuncture (EA) has oncosuppressive and immunomodulatory properties. Here, we investigated the antitumor effects of EA and explored the feasibility of EA combined with anti–PD-1 in MSS colorectal cancer. Results showed that EA exerted its antitumor effect in an intensity-specific manner, and moderate-intensity EA (1.0 mA) induced maximal tumor inhibition. EA enhanced antitumor immune responses by increasing lymphocytes and granzyme B (GzmB) levels, as well as activating the stimulator of IFN genes (STING) pathway. EA combined with anti–PD-1 showed superior efficacy compared with either monotherapy in multiple MSS colorectal cancer mouse models. Single-cell RNA sequencing revealed that cotreatment reprogrammed the tumor immune microenvironment (TIME), as characterized by enhancement of cytotoxic functions. Mechanically, we found that the potentiated effect of EA was dependent upon the STING pathway. Collectively, EA reshapes the TIME of MSS colorectal cancer and sensitizes tumors to anti–PD-1 in a STING pathway–dependent manner. These results provide a mechanistic rationale for using EA as an immunomodulatory strategy to improve the clinical efficacy of anti–PD-1 in MSS colorectal cancer. EA is safe, well-tolerated, and feasible for clinical translation as a promising strategy for treating MSS colorectal cancer.

Funder

National Natural Science Foundation of China

"Tou yan" Action of Heilongjiang province

HMU Marshal Initiative Funding

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Immunology

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