Berberine enhances chemosensitivity to irinotecan in colon cancer via inhibition of NF-κB.

Bibliographic Details
Title: Berberine enhances chemosensitivity to irinotecan in colon cancer via inhibition of NF-κB.
Authors: MEILING YU, XUHUI TONG, BENQUAN QI, HONGDANG QU, SHUYING DONG, BINBIN YU, NAIJU ZHANG, NAN TANG, LINGZHI WANG, CUILING ZHANG
Source: Molecular Medicine Reports; 2014, Vol. 9 Issue 1, p249-254, 6p
Subject Terms: BERBERINE, COLON cancer, APOPTOSIS, IRINOTECAN, CAMPTOTHECIN, FLUOROURACIL, DOXORUBICIN
Abstract: Previous studies have shown that irinotecan (CPT-11) impairs chemotherapy-induced apoptosis by activating nuclear factor κ-B (NF-κB) and a number of strategies have been employed to augment chemosensitivity through the suppression of NF-κB activation. Berberine, a botanical alkaloid, was reported to enhance chemosensitivity to 5-fluorouracil and doxorubicin by suppressing NF-κB activation. In the present study, the effect of berberine on CPT-11 induced apoptosis was investigated through the inhibition of NF-κB. Inhibition of NF-κB activation by p65 small interfering RNA was shown to potentiate apoptosis induced by CPT-11. Berberine suppressed CPT-11 induced NF-κB activation in a dose dependent manner and enhanced chemosensitivity to CPT 11 by downregulating NF κB activation of antiapoptotic genes, c-IAP1, c-IAP2, survivin and Bcl xL. The current observations indicate that berberine inhibits NF-κB activation and may be used to enhance CPT-11 induced apoptosis in colon cancer. [ABSTRACT FROM AUTHOR]
Copyright of Molecular Medicine Reports is the property of Spandidos Publications UK Ltd and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Complementary Index
More Details
ISSN:17912997
DOI:10.3892/mmr.2013.1762
Published in:Molecular Medicine Reports
Language:English