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
Survivin is an inhibitor of apoptosis and, as it is found in many tumors but not in most normal differentiated tissues, is an attractive target for cancer therapy. Survivin expression has been associated with cell proliferation in renal cancer. We previously demonstrated the possibility of treating renal cancer by suppressing survivin expression using the topoisomerase I inhibitor topotecan and survivin-specific siRNA. In the present study, we used Caki-1 cells to investigate the possibility of treating renal cancer by combining topotecan and the hybrid polar compound hexamethylene bisacetamide (HMBA) to completely suppress survivin expression. HMBA is known to induce cell differentiation. This warrants the testing of the ability of HMBA to suppress survivin, which is associated not only with carcinogenesis but also with differentiation. Both topotecan and HMBA were shown to suppress survivin expression and cell proliferation. However, the combination of topotecan and HMBA suppressed survivin expression completely and more effectively inhibited cell proliferation, leading to apoptosis. Combination therapy using topotecan and HMBA might thus be effective treatment for advanced renal cancer.
Download full-text PDF |
Source |
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http://dx.doi.org/10.3892/mmr_00000116 | DOI Listing |
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