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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is a traditional Chinese medicine. The leaves of , specifically the dried leaves of the plant, are commonly consumed as tea in China. In this study, leaves triterpenoids (FLT) were isolated and purified from the dried leaves of , and their in vitro antitumor activity as well as associated molecular mechanisms were systematically investigated. First, the primary components of FLT were determined using high-performance liquid chromatography (HPLC), and the results revealed ursolic acid (70.67%), oleanolic acid (16.23%), and betulinic acid (4.59%) as the major components. Next, the results of the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay showed that FLT exhibited strong antiproliferative activity ( < 0.05) toward human breast cancer MCF-7 and MDA-MB-231 cells. Moreover, the flow cytometry detection of apoptosis using Annexin V-fluorescein isothiocyanate/propidium iodide (Annexin V-FITC/PI) revealed that FLT significantly induced apoptosis in MCF-7 and MDA-MB-231 cells in a dose-dependent manner ( < 0.001). Laser confocal microscopy showed that FLT was mainly located in the mitochondria and lysosome of cells. Meanwhile, after the FLT (15 μg/mL) treatment of MCF-7 and MDA-MB-231 cells, the mitochondrial membrane potential (MMP) ( < 0.001) and intracellular reactive oxygen species (ROS) level ( < 0.001) were significantly reduced. Finally, western blotting demonstrated that FLT (10 and 15 μg/mL) significantly reduced B-cell lymphoma-2 (Bcl-2) ( < 0.001) and cysteinyl aspartate specific proteinase-3 (caspase-3) protein levels ( < 0.001), but significantly increased Bcl-2 homologous antagonist/killer (Bak) protein ( < 0.05 or < 0.001), cleaved-caspase-3 protein ( < 0.001), dynamic-related protein 1 (DRP1), and mitochondrial fission 1 protein (FIS1) levels ( < 0.01 or < 0.001). Taken together, the results indicated that FLT promoted the apoptosis of MCF-7 and MDA-MB-231 cells by activating the mitochondrial pathway. This effect may be attributed to FLT affecting the expression of the Bcl-2 family in mitochondria by promoting DRP1 and FIS1-mediated mitochondrial division, thereby activating the cleavage of caspase-3 and ultimately leading to cell apoptosis.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12318826 | PMC |
http://dx.doi.org/10.1002/fsn3.70664 | DOI Listing |