Gemcitabine combined with gum mastic causes potent growth inhibition and apoptosis of pancreatic cancer cells
Aim: To investigate the antiproliferative and apoptotic effects of gemcitabine combined with gum mastic and the underlying mechanisms in human pancreatic cancer cell lines. Methods: Cell proliferation and apoptosis were examined using the methyl thiazolyl tetrazolium (MTT) assay and propidium iodine...
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Published in | Acta pharmacologica Sinica Vol. 31; no. 6; pp. 741 - 745 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.06.2010
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Aim: To investigate the antiproliferative and apoptotic effects of gemcitabine combined with gum mastic and the underlying mechanisms in human pancreatic cancer cell lines. Methods: Cell proliferation and apoptosis were examined using the methyl thiazolyl tetrazolium (MTT) assay and propidium iodine staining, respectively. The expression of Bcl-2, Bax, NF-KB p65 subunit, and IKBC( protein was measured using Western blotting. Results: Gemcitabine 0.01-100 pg/mL inhibited cell proliferation and induced apoptosis in both pancreatic cancer BxPC-3 and COLO 357 cells. Gum mastic 40 pg/mL significantly potentiated the antiproliferative and apoptotic effects of gemcitabine 10 μg/mL after 72-h treatment. When cells were treated with gemcitabine in combination with gum mastic, the IKBα level was increased, whereas NF-κB activation was blocked; the expression of Bax protein was substantially increased, but Bcl-2 protein was down-regulated. Conclusion: Gemcitabine combined with gum mastic causes potent apoptosis in pancreatic cancer cells. The combination may be an effective therapeutic strategy for pancreatic cancer. |
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Bibliography: | Bcl-2 pancreatic cancer Q255 gum mastic Bax gemcitabine; gum mastic; pancreatic cancer; apoptosis; NF-kappaB; Bcl-2; Bax apoptosis gemcitabine NF-kappaB Q813 31-1347/R These authors contributed equally to the article. |
ISSN: | 1671-4083 1745-7254 |
DOI: | 10.1038/aps.2010.54 |