Role of SERCA3 in the Prognosis and Immune Function in Pan-Cancer

Author:

Li Jiajia12ORCID,Li Xionghui3,Huang Hong4,Tao Lijian2,Zhang Chenzi5ORCID,Xie Yanyun2ORCID,Jiang Yupeng1ORCID

Affiliation:

1. Department of Oncology, The Second Xiangya Hospital, Central South University, Changsha 410008, China

2. Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008, China

3. Department of Critical Medicine, Hunan Provincial Hospital of Integrated Traditional Chinese and Western Medicine, Changsha 410008, China

4. Guilin Medical University, Guilin 541000, China

5. Department of Hematology, Xiangya Hospital, Central South University, Changsha 410008, China

Abstract

The sarcoendoplasmic reticulum calcium adenosine triphosphatase (ATPase) 3 (SERCA3), a member of the SERCA protein family, is located at the endoplasmic reticulum. Its main function is to pump Ca2+ into the endoplasmic reticulum and is involved in maintaining intracellular calcium homeostasis and signal transduction, which are very important factors impacting cancer development and progression. However, the specific role of SERCA3 in cancer remains unclear. Our study, for the first time, comprehensively analyzed the SERCA3 expression profile in multiple cancers and its prognostic value in different cancers using bioinformatics. Furthermore, TCGA database was applied to evaluate the certain correlation of SERCA3 expression with immune modulator genes, immune checkpoints, immune cell infiltration, TMB, and MSI. The results revealed that in many cancers, SERCA3 expression was markedly decreased, which was related to poor prognosis. Additionally, we noticed that SERCA3 expression was correlated with TNM classification and WHO cancer stages in some cancer types. The Pearson correlation analysis showed that SERCA3 expression was closely associated with chemokines, chemokine receptors, MHC, immune activation genes, and immunosuppressive genes. In most cancer types, SERCA3 expression was also associated with immune checkpoints, including PDCD1 and CTLA-4. Further analysis suggested that SERCA3 was significantly correlated with CD8+ T cells, and regulatory T cells. Additionally, pan-cancer analysis confirmed that SERCA3 expression was related to TMB and MSI. In conclusion, these results offer a new insight into the functions and effects of SERCA3 in pan-cancer, and further provide some basis for considering SERCA3 as a potential cancer treatment target and biomarker.

Funder

Hunan Provincial Postdoctoral Science Foundation

Publisher

Hindawi Limited

Subject

Oncology

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