High Mobility Group Box Protein 1 Serves as a Potential Prognostic Marker of Lung Cancer and Promotes Its Invasion and Metastasis by Matrix Metalloproteinase-2 in a Nuclear Factor-κB-Dependent Manner

Author:

Wu Xiaojin1,Wang Weitao2ORCID,Chen Yuanyuan1,Liu Xiangqun3,Wang Jindong4,Qin Xiaobin5,Yuan Dawei2,Yu Tao5,Chen Guangxia6,Mi Yanyan7,Mou Jie7,Cui Jinpeng8,Hu Ankang9,E Yunxiang5,Pei Dongsheng10ORCID

Affiliation:

1. Department of Radiation Oncology, The First People’s Hospital of Xuzhou, Xuzhou, Jiangsu 221002, China

2. Geneis Beijing Co., Ltd., Beijing 100102, China

3. Department of Respiratory Diseases, The First People’s Hospital of Xuzhou, Xuzhou, Jiangsu 221002, China

4. Department of Chest Surgery, The First People’s Hospital of Xuzhou, Xuzhou, Jiangsu 221002, China

5. Department of Tumor, The First People’s Hospital of Xuzhou, Xuzhou, Jiangsu 221002, China

6. Department of Gastroenterology, The First People’s Hospital of Xuzhou, Xuzhou, Jiangsu 221002, China

7. Department of Pharmacy, Xuzhou Medical College, Xuzhou, Jiangsu 221004, China

8. Clinical Laboratory of Yantaishan Hospital, No. 91, Jiefang Road, Yantai, Shandong 264001, China

9. Laboratory Animal Center, Xuzhou Medical College, Xuzhou, Jiangsu 221004, China

10. Department of Pathology, Xuzhou Medical College, Xuzhou, Jiangsu 221004, China

Abstract

Several studies have reported a significant role of high mobility group box protein 1 (HMGB1) in lung cancer. Nevertheless, there is a lack of knowledge regarding the expression of HMGB1 and its correlation with the clinicopathological features of lung cancer. In addition, the potential molecular mechanisms underlying the role of HMGB1 in lung cancer are still unknown. We therefore investigated the clinicopathological and prognostic significance as well as the potential role of HMGB1 in the development and progression of lung cancer. HMGB1 expression in the tumor tissues of the cohort correlated with clinicopathological features. Moreover, lung cell migration and invasion were significantly increased after treatment with HMGB1. The matrix metalloproteinase-2 (MMP-2) expression and activity were upregulated after treatment with HMGB1, while the upregulated expression of MMP-2 stimulated by HMGB1 in lung cancer cells was significantly reduced with the blockage of si-p65. These results indicated that HMGB1 expression was significantly associated with lung cancer progression. We also showed that HMGB1 promoted lung cancer invasion and metastasis by upregulating the expression and activity of MMP-2 in an NF-κB-dependent manner. Taken together, these data suggested that HMGB1 may be a potential prognosis and therapeutic marker for lung cancer.

Funder

Foundation of Jiangsu Provincial Commission of Health and Family Planning

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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