Identification of Downregulated Exosome-Associated Gene ENPP1 as a Novel Lipid Metabolism and Immune-Associated Biomarker for Hepatocellular Carcinoma

Author:

Li Zhilan.1ORCID,He Qingchun.234ORCID,Peng Jinwu.5ORCID,Yan Yuanliang.6ORCID,Fu Chencheng.1ORCID

Affiliation:

1. Department of Pathology, Xiangya Changde Hospital, Changde, China

2. Department of Emergency, Xiangya Hospital, Central South University, Changsha, China

3. Department of Emergency, Xiangya Changde Hospital, Changde, China

4. National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China

5. Department of Pathology, Xiangya Hospital, Central South University, Changsha, China

6. Department of Pharmacy, Xiangya Hospital, Central South University, Changsha, China

Abstract

Exosome plays an important role in the occurrence and development of tumors, such as hepatocellular carcinoma (LIHC). However, the functions and mechanisms of exosome-associated molecules in LIHC are still underexplored. Here, we investigated the role of the exosome-related gene ENPP1 in LIHC. Comprehensive bioinformatics from multiple databases revealed that ENPP1 was significantly downregulated in LIHC tissues. The patients with downregulated ENPP1 displayed a poor prognosis. Immunohistochemistry (IHC) was used to further confirm the downregulated ENPP1 in LIHC tissues. In addition, the coexpression network of ENPP1 was also explored to understand its roles in the underlying signaling pathways, including fatty acid degradation and the PPAR signaling pathway. Simultaneously, GSEA analysis indicated the potential roles of ENPP1 in the lipid metabolism-associated signaling pathways in the pathogenesis of LIHC, including fatty acid metabolism, fatty acid synthesis, and so on. Finally, immunological analysis indicated that ENPP1 might also be involved in multiple immune-related features, including immunoinhibitors, immunostimulators, and chemokines. Taken together, these findings could enhance our understanding of ENPP1 in LIHC pathogenesis and immune response and provide a new target for ENPP1-related immunotherapy in clinical treatment.

Funder

Natural Science Foundation of Hunan Province

Publisher

Hindawi Limited

Subject

Oncology

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