Silibinin sensitizes chemo-resistant breast cancer cells to chemotherapy

Context: Multiple drug resistance is the major obstacle to conventional chemotherapy. Silibinin, a nontoxic naturally occurring compound, has anticancer activity and can increase the cytotoxic effects of chemotherapy in various cancer models. Objective: To evaluate the effects of silibinin on enhanc...

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Main Authors: Ommoleila Molavi, Farzaneh Narimani, Farshid Asiaee, Simin Sharifi, Vahideh Tarhriz, Ali Shayanfar, Mohammadsaied Hejazi, Raymond Lai
Format: Article
Language:English
Published: Taylor & Francis Group 2017-01-01
Series:Pharmaceutical Biology
Subjects:
Online Access:http://dx.doi.org/10.1080/13880209.2016.1270972
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spelling doaj-bca47891e34143498b22d5699b71b62f2020-11-25T03:13:32ZengTaylor & Francis GroupPharmaceutical Biology1388-02091744-51162017-01-0155172973910.1080/13880209.2016.12709721270972Silibinin sensitizes chemo-resistant breast cancer cells to chemotherapyOmmoleila Molavi0Farzaneh Narimani1Farshid Asiaee2Simin Sharifi3Vahideh Tarhriz4Ali Shayanfar5Mohammadsaied Hejazi6Raymond Lai7Tabriz University of Medical SciencesTabriz University of Medical SciencesTabriz University of Medical SciencesTabriz University of Medical SciencesTabriz University of Medical SciencesTabriz University of Medical SciencesTabriz University of Medical SciencesUniversity of AlbertaContext: Multiple drug resistance is the major obstacle to conventional chemotherapy. Silibinin, a nontoxic naturally occurring compound, has anticancer activity and can increase the cytotoxic effects of chemotherapy in various cancer models. Objective: To evaluate the effects of silibinin on enhancing the sensitivity of chemo-resistant human breast cell lines to doxorubicin (DOX) and paclitaxel (PAC). Materials and methods: The cells were treated with silibinin (at 50 to 600 μM concentrations) and/or chemo drugs for 24 and 48 h, then cell viability and changes in oncogenic proteins were determined by MTT assay and Western blotting/RT-PCR, respectively. Flow cytometry was used to study apoptosis in the cells receiving different treatments. The antitumorigenic effects of silibinin (at 200 to 400 μM concentration) were evaluated by mammosphere assay. Results: Silibinin exerted significant growth inhibitory effects with IC50 ranging from 200 to 570 μM in different cell lines. Treatment of DOX-resistant MDA-MB-435 cells with silibinin at 200 μM reduced DOX IC50 from 71 to 10 μg/mL and significantly suppressed the key oncogenic pathways including STAT3, AKT, and ERK in these cells. Interestingly treatment of DOX-resistant MDA-MB-435 cells with silibinin at 400 μM concentration for 48 h induced a 50% decrease in the numbers of colonies as compared with DMSO-treated cells. Treatment of PAC-resistant MCF-7 cells with silibinin at 400 μM concentration generated synergistic effects when it was used in combination with PAC at 250 nM concentration (CI = 0.81). Conclusion: Silibinin sensitizes chemo-resistant cells to chemotherapeutic agents and can be useful in treating breast cancers.http://dx.doi.org/10.1080/13880209.2016.1270972resistancedoxorubicinpaclitaxelapoptosisstat3 pathway
collection DOAJ
language English
format Article
sources DOAJ
author Ommoleila Molavi
Farzaneh Narimani
Farshid Asiaee
Simin Sharifi
Vahideh Tarhriz
Ali Shayanfar
Mohammadsaied Hejazi
Raymond Lai
spellingShingle Ommoleila Molavi
Farzaneh Narimani
Farshid Asiaee
Simin Sharifi
Vahideh Tarhriz
Ali Shayanfar
Mohammadsaied Hejazi
Raymond Lai
Silibinin sensitizes chemo-resistant breast cancer cells to chemotherapy
Pharmaceutical Biology
resistance
doxorubicin
paclitaxel
apoptosis
stat3 pathway
author_facet Ommoleila Molavi
Farzaneh Narimani
Farshid Asiaee
Simin Sharifi
Vahideh Tarhriz
Ali Shayanfar
Mohammadsaied Hejazi
Raymond Lai
author_sort Ommoleila Molavi
title Silibinin sensitizes chemo-resistant breast cancer cells to chemotherapy
title_short Silibinin sensitizes chemo-resistant breast cancer cells to chemotherapy
title_full Silibinin sensitizes chemo-resistant breast cancer cells to chemotherapy
title_fullStr Silibinin sensitizes chemo-resistant breast cancer cells to chemotherapy
title_full_unstemmed Silibinin sensitizes chemo-resistant breast cancer cells to chemotherapy
title_sort silibinin sensitizes chemo-resistant breast cancer cells to chemotherapy
publisher Taylor & Francis Group
series Pharmaceutical Biology
issn 1388-0209
1744-5116
publishDate 2017-01-01
description Context: Multiple drug resistance is the major obstacle to conventional chemotherapy. Silibinin, a nontoxic naturally occurring compound, has anticancer activity and can increase the cytotoxic effects of chemotherapy in various cancer models. Objective: To evaluate the effects of silibinin on enhancing the sensitivity of chemo-resistant human breast cell lines to doxorubicin (DOX) and paclitaxel (PAC). Materials and methods: The cells were treated with silibinin (at 50 to 600 μM concentrations) and/or chemo drugs for 24 and 48 h, then cell viability and changes in oncogenic proteins were determined by MTT assay and Western blotting/RT-PCR, respectively. Flow cytometry was used to study apoptosis in the cells receiving different treatments. The antitumorigenic effects of silibinin (at 200 to 400 μM concentration) were evaluated by mammosphere assay. Results: Silibinin exerted significant growth inhibitory effects with IC50 ranging from 200 to 570 μM in different cell lines. Treatment of DOX-resistant MDA-MB-435 cells with silibinin at 200 μM reduced DOX IC50 from 71 to 10 μg/mL and significantly suppressed the key oncogenic pathways including STAT3, AKT, and ERK in these cells. Interestingly treatment of DOX-resistant MDA-MB-435 cells with silibinin at 400 μM concentration for 48 h induced a 50% decrease in the numbers of colonies as compared with DMSO-treated cells. Treatment of PAC-resistant MCF-7 cells with silibinin at 400 μM concentration generated synergistic effects when it was used in combination with PAC at 250 nM concentration (CI = 0.81). Conclusion: Silibinin sensitizes chemo-resistant cells to chemotherapeutic agents and can be useful in treating breast cancers.
topic resistance
doxorubicin
paclitaxel
apoptosis
stat3 pathway
url http://dx.doi.org/10.1080/13880209.2016.1270972
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