S100A8 as a Promising Biomarker and Oncogenic Immune Protein in the Tumor Microenvironment: An Integrative Pancancer Analysis

Author:

Wu Zixuan1ORCID,Jiang Dongli2ORCID,Huang Xuyan1ORCID,Cai Minjie3ORCID,Yuan Kai4ORCID,Huang Peidong4ORCID

Affiliation:

1. Guangzhou University of Chinese Medicine, Guangzhou, Guangdong Province, 510006S, China

2. The Fifth Affiliated Hospital of Southern Medical University, Guangzhou, Guangdong Province, 510009, China

3. Shantou Health School, Shantou, Guangdong Province, 515061, China

4. Yunnan University of Chinese Medicine, Kunming, Yunnan Province, 650500, China

Abstract

Background. S100 Calcium Binding Protein A8 (S100A8) is beneficial for cancer immunotherapy. However, the processes underlying its therapeutic potential have not been completely studied. Methods. The Cancer Genome Atlas provides raw data on 33 different cancer types. GEO made available GSE67501, GSE78220, and IMvigor210. We investigated S100A8’s genetic changes, expression patterns, and survival studies. The linkages between S100A8 and TME, as well as its association with immunological processes/elements and the major histocompatibility complex, were explored to effectively understand the role of S100A8 in cancer immunotherapy. Three distinct immunotherapeutic cohorts were employed to examine the relationship between S100A8 and immunotherapeutic response. Results. S100A8 expression was high in tumor tissue. The overexpression of S100A8 is associated with poor clinical outcome in patients with overall survival. S100A8 is associated with immune cell infiltration, immunological modulators, and immunotherapeutic indicators. S100A8 overexpression is connected to immune-related pathways. However, no statistically significant connection between S100A8 and immunotherapeutic response was identified. Conclusions. S100A8 may be a reliable biomarker for tumor prognosis and a viable prospective therapeutic target for human cancer immunotherapy (e.g., GBM, KIRC, LGG, and LIHC).

Funder

Kaiyuan

Publisher

Hindawi Limited

Subject

Oncology

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