<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang X</submitter><funding>Shanghai Hospital Development Center</funding><pagination>6258268</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8811541</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>2022</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Recent studies have shown that the expression level of triosephosphate isomerase 1 (&lt;i>TPI1&lt;/i>) may be associated with the occurrence and metastasis of tumors, but the expression level of &lt;i>TPI1&lt;/i> and its effect on lung adenocarcinoma (LUAD) and squamous cell carcinoma (LUSC) are not yet clear.&lt;h4>Methods&lt;/h4>We comprehensively explored and validated the &lt;i>TPI1&lt;/i> expression in lung adenocarcinoma and lung squamous cell carcinoma in public datasets. The associations of &lt;i>TPI1&lt;/i> expression with clinicopathological characteristics and prognosis were also studied in both histological types. Moreover, we analyzed the potential relations of &lt;i>TPI1&lt;/i> with immunomodulators and immune cell infiltrations in the tumor microenvironment based on previous literatures and bioinformatic tools.&lt;h4>Results&lt;/h4>We found that &lt;i>TPI1&lt;/i> was significantly overexpressed in LUAD and LUSC. Significant associations of &lt;i>TPI1&lt;/i> expression were observed regarding age, gender, and pathological stages in LUAD. However, similar trend was only found with respect to age in LUSC. The high expression of &lt;i>TPI1&lt;/i> was significantly associated with worse survival in LUAD, but not in LUSC. Furthermore, we explored the potential distribution and changes of &lt;i>TPI1&lt;/i> expression in tumor microenvironment. Pathway enrichment analyses were performed to identify possible roles of &lt;i>TPI1&lt;/i> in both lung cancers.&lt;h4>Conclusions&lt;/h4>&lt;i>TPI1&lt;/i> was overexpressed in both LUAD and LUSC. Increased &lt;i>TPI1&lt;/i> expression was correlated with poor prognosis in LUAD and changed immune cell infiltrating in various degrees in both histological types. Our study provides insights in understanding the potential roles of &lt;i>TPI1&lt;/i> in tumor progression and immune microenvironment.</pubmed_abstract><journal>Disease markers</journal><pubmed_title>Systemic Analyses of the Expression of TPI1 and Its Associations with Tumor Microenvironment in Lung Adenocarcinoma and Squamous Cell Carcinoma.</pubmed_title><pmcid>PMC8811541</pmcid><funding_grant_id>SHDC2020CR4028</funding_grant_id><funding_grant_id>18CG19</funding_grant_id><funding_grant_id>20QA1408300</funding_grant_id><funding_grant_id>82000084</funding_grant_id><funding_grant_id>81802256</funding_grant_id><funding_grant_id>FKYQ1907</funding_grant_id><funding_grant_id>21YF1438600</funding_grant_id><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Zheng H</pubmed_authors><pubmed_authors>Dai C</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Ye C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Systemic Analyses of the Expression of TPI1 and Its Associations with Tumor Microenvironment in Lung Adenocarcinoma and Squamous Cell Carcinoma.</name><description>&lt;h4>Background&lt;/h4>Recent studies have shown that the expression level of triosephosphate isomerase 1 (&lt;i>TPI1&lt;/i>) may be associated with the occurrence and metastasis of tumors, but the expression level of &lt;i>TPI1&lt;/i> and its effect on lung adenocarcinoma (LUAD) and squamous cell carcinoma (LUSC) are not yet clear.&lt;h4>Methods&lt;/h4>We comprehensively explored and validated the &lt;i>TPI1&lt;/i> expression in lung adenocarcinoma and lung squamous cell carcinoma in public datasets. The associations of &lt;i>TPI1&lt;/i> expression with clinicopathological characteristics and prognosis were also studied in both histological types. Moreover, we analyzed the potential relations of &lt;i>TPI1&lt;/i> with immunomodulators and immune cell infiltrations in the tumor microenvironment based on previous literatures and bioinformatic tools.&lt;h4>Results&lt;/h4>We found that &lt;i>TPI1&lt;/i> was significantly overexpressed in LUAD and LUSC. Significant associations of &lt;i>TPI1&lt;/i> expression were observed regarding age, gender, and pathological stages in LUAD. However, similar trend was only found with respect to age in LUSC. The high expression of &lt;i>TPI1&lt;/i> was significantly associated with worse survival in LUAD, but not in LUSC. Furthermore, we explored the potential distribution and changes of &lt;i>TPI1&lt;/i> expression in tumor microenvironment. Pathway enrichment analyses were performed to identify possible roles of &lt;i>TPI1&lt;/i> in both lung cancers.&lt;h4>Conclusions&lt;/h4>&lt;i>TPI1&lt;/i> was overexpressed in both LUAD and LUSC. Increased &lt;i>TPI1&lt;/i> expression was correlated with poor prognosis in LUAD and changed immune cell infiltrating in various degrees in both histological types. Our study provides insights in understanding the potential roles of &lt;i>TPI1&lt;/i> in tumor progression and immune microenvironment.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2024-11-20T02:28:05.463Z</modification><creation>2024-11-20T02:28:05.463Z</creation></dates><accession>S-EPMC8811541</accession><cross_references><pubmed>35126788</pubmed><doi>10.1155/2022/6258268</doi></cross_references></HashMap>