PYRROLIDINE DITHIOCARBAMATE INHIBITS NF-KB ACTIVATION AND ENHANCES TNF-INDUCED APOPTOSIS IN HUMAN BREAST CANCER CELLS
TUGang, YAOZhen-xiang
Abstract
TUGang, YAOZhen-xiang
Abstract
Objective: To determine whether pyrrolidine dithio-carbamate(PDTC) enhances TNFα-induced apoptosis in cultured breast cancer cells and explore the role of NF-κB in TNFα-induced apoptosis. Methods: Human breast cancer cell lines MCF-7 and MDA-MB-435s were treated with TNFα, PDTC and combination therapy. Cell survivals were determined by MTT assay. Apoptosis was detected by TUNEL and flow cytometry. NF-κB DNA binding activity was detected using electrophoresis mobility shift assay (EMSA). Western blots were performed to demonstrate IκBα(Inhibitor protein of nuclear factorκB) phosphorylation and degradation. Results: Cell growth was not suppressed by either TNFα(2000 U/ml or less) or PDTC alone. Both cell lines treated with TNFα(2000 U/ml) combined with PDTC(50 μmol/L) showed significant growth inhibition. PDTC inhibited TNFα-induced IκBα phosphorylation and degradation in both cell lines. EMSA showed that PDTC continuously inhibited TNFα induced NF-κB DNA binding activity. TNFα induced apoptosis(TUNEL) was increased significantly when both cells were pretreated with PDTC, and this was confirmed by Flow cytometry. Conclusion: PDTC enhances TNFα-induced apoptosis via inhibiting IκBα phosphorylation and degradation in human breast cancer cells. NF-κB protects against TNFα-induced apoptosis.
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Objective: To determine whether pyrrolidine dithio-carbamate(PDTC) enhances TNFα-induced apoptosis in cultured breast cancer cells and explore the role of NF-κB in TNFα-induced apoptosis. Methods: Human breast cancer cell lines MCF-7 and MDA-MB-435s were treated with TNFα, PDTC and combination therapy. Cell survivals were determined by MTT assay. Apoptosis was detected by TUNEL and flow cytometry. NF-κB DNA binding activity was detected using electrophoresis mobility shift assay (EMSA). Western blots were performed to demonstrate IκBα(Inhibitor protein of nuclear factorκB) phosphorylation and degradation. Results: Cell growth was not suppressed by either TNFα(2000 U/ml or less) or PDTC alone. Both cell lines treated with TNFα(2000 U/ml) combined with PDTC(50 μmol/L) showed significant growth inhibition. PDTC inhibited TNFα-induced IκBα phosphorylation and degradation in both cell lines. EMSA showed that PDTC continuously inhibited TNFα induced NF-κB DNA binding activity. TNFα induced apoptosis(TUNEL) was increased significantly when both cells were pretreated with PDTC, and this was confirmed by Flow cytometry. Conclusion: PDTC enhances TNFα-induced apoptosis via inhibiting IκBα phosphorylation and degradation in human breast cancer cells. NF-κB protects against TNFα-induced apoptosis.
Key concepts: Pyrrolidine dithiocarbamate, Apoptosis, Tumor necrosis factor alpha, Molecular biology, Electrophoretic mobility shift assay, TUNEL assay, Chemistry, Flow cytometry