Low-Temperature Plasma-Activated Medium Inhibited Proliferation and Progression of Lung Cancer by Targeting the PI3K/Akt and MAPK Pathways

Author:

Li Ying1ORCID,Lv Yang2ORCID,Zhu Yu34ORCID,Yang Xiaodong3ORCID,Lin Boya3ORCID,Li Mengqing3ORCID,Zhou Yaqi5ORCID,Tan Zhibo6ORCID,Choi Eun Ha7ORCID,Wang Junjie8ORCID,Wang Shubin3ORCID,Liu Yajie1ORCID

Affiliation:

1. Department of Radiation Oncology, Shenzhen Key Laboratory of Gastrointestinal Cancer Translational Research, Cancer Institute, Peking University Shenzhen Hospital, Shenzhen Peking University-Hong Kong University of Science & Technology Medical Center, Shenzhen 518036, China

2. State Key Laboratory of Advanced Electromagnetic Engineering and Technology, Huazhong University of Science and Technology, Wuhan 430030, China

3. Department of Oncology, Shenzhen Key Laboratory of Gastrointestinal Cancer Translational Research, Cancer Institute, Peking University Shenzhen Hospital, Shenzhen 518036, China

4. Accurate International Biotechnology (GZ) Co. Ltd., Guangzhou 510700, China

5. Department of Otorhinolaryngology, Peking University Shenzhen Hospital, Shenzhen 518036, China

6. Department of Radiation Oncology, Peking University Shenzhen Hospital, Shenzhen 518036, China

7. Department of Electrical and Biological Physics, Plasma Bioscience Research Center, Applied Plasma Medicine Center, Kwangwoon University, Seoul 01897, Republic of Korea

8. Department of Radiation Oncology, Peking University Third Hospital, Beijing 100083, China

Abstract

Low-temperature plasma, an engineered technology to generate various reactive species, is actively studied in cancer treatment in recent years, yet mainly by using a traditional 2D cell culture system. In this study, we explored the effect of the plasma-activated medium (PAM) on lung cancer cells in vitro and in vivo by using a 3D cell culture model. The results showed that PAM markedly inhibited 3D spheroid formation and downregulated stemness-related gene expression. We found that reactive oxygen species (ROS) penetrated throughout the whole spheroids and induced cell death surrounding and in the core of the tumor spheroid. Besides, PAM treatment suppressed migration and invasion of lung cancer cells and downregulated epithelial-mesenchymal transition- (EMT-) related gene expression. In the mouse xenograft model, the tumor volume was significantly smaller in the PAM-treated group compared with the control group. By using transcriptome sequencing, we found that PI3K/Akt and MAPK pathways were involved in the inhibition effects of PAM on lung cancer cells. Therefore, our results indicated that PAM exhibits potential anticancer effects on lung cancer and provides insight into further exploration of PAM-induced cell death and translational preclinical use.

Funder

Sanming Project of Medicine in Shenzhen

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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