Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1075
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3195
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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The tow-pore domain (KCNK) potassium channel family is associated with tumor progression, but its prognostic value in lung adenocarcinoma (LUAD) remains unclear. In this study, we integrated data from the TCGA and GEO databases to identify 9 KCNK-related differentially expressed genes, and based on this, we classified two molecular subtypes with significantly different prognoses. A 11-gene prognostic model with independent prognostic value was constructed through regression analysis. Immuno-analysis revealed that the low-risk group had stronger immune infiltration and might be more suitable for immunotherapy. These findings reveal the prognostic significance of the KCNK genes and provide a reference for immunotherapy.
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http://dx.doi.org/10.1080/10255842.2025.2532809 | DOI Listing |