Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Background: Worldwide, lung squamous cell carcinoma (LUSC) has wreaked havoc on humanity. Matrix metallopeptidase 12 () plays an essential role in a variety of cancers. This study aimed to reveal the expression, clinical significance, and potential molecular mechanisms of in LUSC.
Methods: There were 2,738 messenger RNA (mRNA) samples from several multicenter databases used to detect expression in LUSC, and 125 tissue samples were validated by immunohistochemistry (IHC) experiments. Receiver operator characteristic (ROC) curves, Kaplan-Meier curves, and univariate and multivariate Cox regression analyses were used to assess the clinical value of in LUSC. The potential molecular mechanisms of were explored by gene enrichment analysis and immune correlation analysis. Furthermore, single-cell sequencing was used to determine the distribution of in multiple tumor microenvironment cells.
Results: was significantly overexpressed at the mRNA level ( < 0.05, SMD = 3.13, 95% CI [2.51-3.75]), which was verified at the protein level ( < 0.001) by internal IHC experiments. expression could be used to differentiate LUSC samples from normal samples, and overexpression of itself implied a worse clinical prognosis and higher levels of immune cell infiltration in LUSC patients. was involved in cancer development and progression through two immune-related signaling pathways. The high expression of in LUSC might act as an antigen-presenting cell-associated tumor neoantigen and activate the body's immune response.
Conclusions: expression is upregulated in LUSC and high expression of serves as a risk factor for LUSC patients. may be involved in cancer development by participating in immune-related signaling pathways and elevating the level of immune cell infiltration.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439720 | PMC |
http://dx.doi.org/10.7717/peerj.15598 | DOI Listing |
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