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http://purl.uniprot.org/citations/31812070http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31812070http://www.w3.org/2000/01/rdf-schema#comment"

Background

Lung adenocarcinoma (LUAD) is a crucial pathological type of lung cancer. Immune-infiltration of the tumor microenvironment positively associated with overall survival in LUAD. TTC21A is a gene has not reported in cancer, and the mechanism behind it is still unclear. Our study assesses TTC21A role in LUAD, via TCGA data.

Methods

GEPIA was utilized to analyze the expression of TTC21A in LUAD. We evaluated the influence of TTC21A on survival of LUAD patients by survival module. Then, data sets of LUAD were downloaded from TCGA. The correlations between clinical information and TTC21A expression were analyzed using logistic regression. Clinicopathologic characteristics associated with overall survival in TCGA patients using Cox regression. In addition, we explored the correlation between TTC21A and cancer immune infiltrates using CIBERSORT and "Correlation" module of GEPIA.

Results

The univariate analysis using logistic regression, wherein TTC21A expression served as a categorical dependent variable (with a median expression value of 2.5), indicated that increased TTC21A expression is significantly correlated with pathological stage, tumor status and lymph nodes. Moreover, multivariate analysis revealed that the up-regulated TTC21A expression, negative results of pathological stage and distant metastasis are independent prognostic factors for good prognosis. Specifically, a positive correlation between increased TTC21A expression and immune infiltrating level of B cells, Neutrophils, Mast cells and T cells was established using CIBERSORT analysis. Furthermore, we confirmed it in "correlation" module of GEPIA.

Conclusion

Together with all these findings, increased TTC21A expression correlates with favorable prognosis and increased proportion of immune cells, such as B cells, Neutrophils, Mast cells and T cells in LUAD. These conclusions indicate that TTC21A could serve as a potential biomarker to assess prognosis and immune infiltration level in LUAD."xsd:string
http://purl.uniprot.org/citations/31812070http://purl.org/dc/terms/identifier"doi:10.1016/j.intimp.2019.106077"xsd:string
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/author"Huang J."xsd:string
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/author"Ren S."xsd:string
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/author"Wang Z."xsd:string
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/author"Zhang C."xsd:string
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/author"Wang W."xsd:string
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/date"2020"xsd:gYear
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/name"Int Immunopharmacol"xsd:string
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/pages"106077"xsd:string
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/title"Increased expression of TTC21A in lung adenocarcinoma infers favorable prognosis and high immune infiltrating level."xsd:string
http://purl.uniprot.org/citations/31812070http://purl.uniprot.org/core/volume"78"xsd:string
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