Comprehensive analysis of the expression and prognosis for APOE in malignancies: A pan-cancer analysis

Apolipoprotein E ( ), a gene identified as one of the strongest genetic factors contributing to the risk determinant of developing late-onset Alzheimer's disease (AD), may also contribute to the risk of cancer. However, no pan-cancer analysis has been conducted specifically for the gene. In thi...

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Veröffentlicht in:Oncology research 2022-01, Vol.30 (1), p.13-22
Hauptverfasser: Yu, Shoukai, Qian, Lingmei, Ma, Jun
Format: Artikel
Sprache:eng
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Zusammenfassung:Apolipoprotein E ( ), a gene identified as one of the strongest genetic factors contributing to the risk determinant of developing late-onset Alzheimer's disease (AD), may also contribute to the risk of cancer. However, no pan-cancer analysis has been conducted specifically for the gene. In this study, we investigated the oncogenic role of the gene across cancers by GEO (Gene Expression Omnibus) and TCGA (The Cancer Genome Atlas). Based on the available data, we found that most cancer types overexpress , and clear associations exist between the expression level of and prognosis in tumor patients. The expression of also correlates with certain gender-associated tumors including, ovarian cancer, uterine carcinosarcoma, and breast cancer. However, there is a significant negative association between cancer-associated fibroblast infiltration levels and the expression level of in testicular germ cell tumors. Moreover, acute inflammatory response and protein-activation cascade-associated functions play an important role in the functional mechanisms of APOE. The present pan-cancer analysis of APOE shows that the protein phosphorylation, DNA methylation, and genetic alterations of APOE have a significant clinical relevance for survival prognosis and immune cell infiltration. This novel pan-cancer study outlines the current understanding of APOE oncogenic roles across thirty-three cancers and highlights the complex association between AD and cancers.
ISSN:0965-0407
1555-3906
DOI:10.32604/or.2022.026141