4.4 Article

Immune infiltration and prognostic and diagnostic use of LGALS4 in colon adenocarcinoma and bladder urothelial carcinoma

Journal

AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH
Volume 13, Issue 10, Pages 11353-11363

Publisher

E-CENTURY PUBLISHING CORP

Keywords

Omics integration; translational research; immune infiltration; LGALS4; biomarker; BLCA

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Colon adenocarcinoma is a common gastrointestinal tumor with high mortality, and research has identified immune-related genes playing a vital role in its development. The LGALS4 gene is significantly downregulated in COAD and BLCA, serving as a potential prognostic and diagnostic marker for these cancers. This analysis reveals novel drug targets and molecular markers that may help explain the pathogenesis of COAD and BLCA.
Colon adenocarcinoma (COAD) is a common tumor of the gastrointestinal tract with a high mortality rate. Current research has identified many genes associated with immune infiltration that play a vital role in the development of COAD. In this study, we analysed the prognostic and diagnostic features of such immune-related genes in the context of colonic adenocarcinoma (COAD). We analysed 17 overlapping gene expression profiles of COAD and healthy samples obtained from TCGA-COAD and public single-cell sequencing resources, to identify potential therapeutic COAD targets. We evaluated the abundance of immune infiltration with those genes using the TIMER (Tumor Immune Estimation Resource) deconvolution method. Subsequently, we developed predictive and survival models to assess the prognostic value of these genes. The LGALS4 (Galectin-4) gene was found to be significantly (P<0.05) downregulated in COAD and bladder urothelial carcinoma (BLCA) compared to healthy samples. We identified LGALS4 as a prognostic and diagnostic marker for multiple cancer types, including COAD and BLCA. Our analysis reveals a series of novel candidate drug targets, as well as candidate molecular markers, that may explain the pathogenesis of COAD and BLCA. LGALS4 gene is associated with multiple cancer types and is a possible prognostic, as well as diagnostic, marker of COAD and BLCA.

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