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Research Paper|Volume 15, Issue 23|pp 13840—13853

Prognostic significance and immune characteristics of APOE in gastric cancer

Xiulan Peng1, Zhen Cai2, Duansi Chen3, Fei Ye4, Lifeng Hong5
  • 1Department of Oncology, The Second Affiliated Hospital of Jianghan University, Wuhan, Hubei 430050, China
  • 2Department of Operation Room, The Second Affiliated Hospital of Jianghan University, Wuhan, Hubei 430050, China
  • 3Department of Oncology, Suizhou Zengdu Hospital, Suizhou, Hubei 441300, China
  • 4Department of Radiology, The Second Affiliated Hospital of Jianghan University, Wuhan, Hubei 430050, China
  • 5Department of Cardiology, The Second Affiliated Hospital of Jianghan University, Wuhan, Hubei 430050, China
* Equal contribution and co-first authors
Received: June 26, 2023Accepted: October 23, 2023Published: December 4, 2023

Copyright: © 2023 Peng et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

Gastric cancer (GC) is a prevalent malignancy affecting the digestive system, and it is the second leading cause of cancer-related mortality worldwide. Immunotherapy presents a potential lifeline for patients with advanced gastric cancer, emphasizing the need to find new molecular targets that improve the response to immunotherapy. In our research, we conducted a comprehensive bioinformatic analysis to investigate the expression profiles of apolipoprotein E (APOE) transcription. Subsequently, we examined the correlation between APOE transcription and the prognosis of GC patients. Additionally, we evaluated the connection between APOE transcription and immune cells abundance. To validate our findings, we conducted immunohistochemistry experiment to ascertain the level of APOE protein in GC patients and assessed its prognostic role in a cohort of 97 GC individuals. Our results revealed that APOE is increased in GC tissues, and APOE displays diagnostic potential in distinguishing GC from normal tissues. Notably, upregulated APOE expression in GC patients is associated with unfavorable overall survival. Differential APOE expression was further observed across different immune subtypes of GC, indicating its involvement in immune cell activation and infiltration. Moreover, we detected increased APOE protein expression in GC tissues, which exhibited a strong correlation with poor survival outcomes. In light of these findings, APOE has become a crucial prognostic molecular with immunomodulatory function in GC. These results underscore the significance of APOE across various cancer types, including GC, and provide valuable insights into its role from both a bioinformatics and clinical perspective.