کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2480866 | 1556206 | 2013 | 11 صفحه PDF | دانلود رایگان |
Multidrug resistance (MDR) remains a significant problem for effective cancer chemotherapy. In spite of considerable advances in drug discovery, most of the cancer cases still stay incurable because of resistance to chemotherapy. We synthesized a novel, Mn (II) complex (chelate), viz., manganese N-(2-hydroxy acetophenone) glycinate (MnNG) that exhibits considerable efficacy to overcome drug resistant cancer. The antiproliferative activity of MnNG was studied on doxorubicin resistant and sensitive human T lymphoblastic leukemia cells (CEM/ADR 5000 and CCRF/CEM). MnNG induced apoptosis significantly in CEM/ADR 5000 cells probably through generation of reactive oxygen species. Moreover, intraperitoneal (i.p.) application of MnNG at non-toxic doses caused significant increase in the life-span of Swiss albino mice bearing sensitive and doxorubicin resistant subline of Ehrlich ascites carcinoma cells.
Manganese N-(2-hydroxy acetophenone) glycinate (MnNG) has selective potential ability to kill doxorubicin resistant human T lymphoblastic leukemia cells (CEM/ADR 5000) compared to its parental sensitive cell line (CCRF/CEM).Figure optionsDownload high-quality image (80 K)Download as PowerPoint slide
Journal: European Journal of Pharmaceutical Sciences - Volume 49, Issue 4, 16 July 2013, Pages 737–747