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
To investigate whether kaempferol exhibits a protective effect on high glucose-induced epithelial-mesenchymal transition (EMT) by mediating the / and PAK4/β-catenin pathways in SRA01/04 cells. qRT-PCR and western blot assays were used for gene and protein determination, and migration and invasion assays were conducted. A coimmunoprecipitation assay was used for determining protein interactions. High glucose effectively upregulated expression, downregulated expression and promoted cell migration and invasion. Kaempferol attenuated high glucose-induced EMT by increasing expression and decreasing expression. was identified as a direct target of . overexpression could rescue the effects of deficiency on SRA01/04 cells. Kaempferol ameliorated the regulatory effects of / on high glucose-induced EMT through PAK4/β-catenin in SRA01/04 cells.
Download full-text PDF |
Source |
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http://dx.doi.org/10.4155/fmc-2020-0381 | DOI Listing |
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