Evaluation of gamma radiation-induced cytotoxicity of breast cancer cells: Is there a time-dependent dose with high efficiency?

Context: Radiotherapy is one of the important treatment modalities in the management of breast cancer. Aims: The aim of this study is to study the efficient treatment of breast cancer as related to the dose delivery. Materials and Methods: The human breast cancer cell lines (MCF-7) cells were cultur...

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Veröffentlicht in:Indian journal of cancer 2016-01, Vol.53 (1), p.25-28
Hauptverfasser: Fazel, M, Mehnati, P, Baradaran, B, Pirayesh, J
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container_title Indian journal of cancer
container_volume 53
creator Fazel, M
Mehnati, P
Baradaran, B
Pirayesh, J
description Context: Radiotherapy is one of the important treatment modalities in the management of breast cancer. Aims: The aim of this study is to study the efficient treatment of breast cancer as related to the dose delivery. Materials and Methods: The human breast cancer cell lines (MCF-7) cells were cultured and exposed by 1, 2, 4, 6, 8, 10, and 20 Gy of γ-rays. Radiation-induced cell death was detected and evaluated, using three assay methods: Cell viability, clonogenic cell survival assay and induction of apoptosis. The cell viability was determined using trypan blue staining, 24 and 72 h post-irradiation. The survival fraction (SF) was determined by colony counting, 14 days after exposure and the apoptotic cell death was determined using the TUNEL assay. Statistical Analysis Used: One- or two-way analysis of variance was deemed as appropriate, followed by relevant post t-test to determine P values. Results: The difference of MCF-7 cell death through increasing post-radiation time from 24 to 72 h following the dose of 1, 6 and 10 Gy was found to be 2%, 9.6% and 7.14%, respectively. D0of MCF-7 was 220 cGy and the SF in the cells irradiated by 1 Gy and 10 Gy doses were 0.8 and 0.0001, respectively. The estimated variances were 2%, 11.1% and 8.4%, between 24 h and 72 h post-radiation apoptosis death for 1, 6, and 10 Gy, respectively. Conclusions: The dose and time dependence inducing apoptotic death was significant (P = 0.001). The delayed mortality and apoptosis was observed in MCF-7 cell, but the variance of total cell death and apoptosis in 24 and 72 h post-radiation with 6 Gy was obviously more than that with other doses.
doi_str_mv 10.4103/0019-509X.180862
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Aims: The aim of this study is to study the efficient treatment of breast cancer as related to the dose delivery. Materials and Methods: The human breast cancer cell lines (MCF-7) cells were cultured and exposed by 1, 2, 4, 6, 8, 10, and 20 Gy of γ-rays. Radiation-induced cell death was detected and evaluated, using three assay methods: Cell viability, clonogenic cell survival assay and induction of apoptosis. The cell viability was determined using trypan blue staining, 24 and 72 h post-irradiation. The survival fraction (SF) was determined by colony counting, 14 days after exposure and the apoptotic cell death was determined using the TUNEL assay. Statistical Analysis Used: One- or two-way analysis of variance was deemed as appropriate, followed by relevant post t-test to determine P values. Results: The difference of MCF-7 cell death through increasing post-radiation time from 24 to 72 h following the dose of 1, 6 and 10 Gy was found to be 2%, 9.6% and 7.14%, respectively. D0of MCF-7 was 220 cGy and the SF in the cells irradiated by 1 Gy and 10 Gy doses were 0.8 and 0.0001, respectively. The estimated variances were 2%, 11.1% and 8.4%, between 24 h and 72 h post-radiation apoptosis death for 1, 6, and 10 Gy, respectively. Conclusions: The dose and time dependence inducing apoptotic death was significant (P = 0.001). The delayed mortality and apoptosis was observed in MCF-7 cell, but the variance of total cell death and apoptosis in 24 and 72 h post-radiation with 6 Gy was obviously more than that with other doses.</description><identifier>ISSN: 0019-509X</identifier><identifier>EISSN: 1998-4774</identifier><identifier>DOI: 10.4103/0019-509X.180862</identifier><identifier>PMID: 27146733</identifier><language>eng</language><publisher>India: Wolters Kluwer - Medknow Publications</publisher><subject>Apoptosis ; Apoptosis - radiation effects ; Breast cancer ; Breast Neoplasms - pathology ; Breast Neoplasms - radiotherapy ; Cancer therapies ; Care and treatment ; Colonies &amp; territories ; Deoxyribonucleic acid ; DNA ; Dose-response relationship ; Dose-Response Relationship, Radiation ; Efficiency ; Female ; Gamma Rays - therapeutic use ; Humans ; Laboratories ; MCF-7 Cells ; Methods ; Mortality ; Observations ; Patient outcomes ; Radiation therapy ; Radiotherapy ; Studies</subject><ispartof>Indian journal of cancer, 2016-01, Vol.53 (1), p.25-28</ispartof><rights>COPYRIGHT 2016 Medknow Publications and Media Pvt. 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Aims: The aim of this study is to study the efficient treatment of breast cancer as related to the dose delivery. Materials and Methods: The human breast cancer cell lines (MCF-7) cells were cultured and exposed by 1, 2, 4, 6, 8, 10, and 20 Gy of γ-rays. Radiation-induced cell death was detected and evaluated, using three assay methods: Cell viability, clonogenic cell survival assay and induction of apoptosis. The cell viability was determined using trypan blue staining, 24 and 72 h post-irradiation. The survival fraction (SF) was determined by colony counting, 14 days after exposure and the apoptotic cell death was determined using the TUNEL assay. Statistical Analysis Used: One- or two-way analysis of variance was deemed as appropriate, followed by relevant post t-test to determine P values. Results: The difference of MCF-7 cell death through increasing post-radiation time from 24 to 72 h following the dose of 1, 6 and 10 Gy was found to be 2%, 9.6% and 7.14%, respectively. D0of MCF-7 was 220 cGy and the SF in the cells irradiated by 1 Gy and 10 Gy doses were 0.8 and 0.0001, respectively. The estimated variances were 2%, 11.1% and 8.4%, between 24 h and 72 h post-radiation apoptosis death for 1, 6, and 10 Gy, respectively. Conclusions: The dose and time dependence inducing apoptotic death was significant (P = 0.001). 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Aims: The aim of this study is to study the efficient treatment of breast cancer as related to the dose delivery. Materials and Methods: The human breast cancer cell lines (MCF-7) cells were cultured and exposed by 1, 2, 4, 6, 8, 10, and 20 Gy of γ-rays. Radiation-induced cell death was detected and evaluated, using three assay methods: Cell viability, clonogenic cell survival assay and induction of apoptosis. The cell viability was determined using trypan blue staining, 24 and 72 h post-irradiation. The survival fraction (SF) was determined by colony counting, 14 days after exposure and the apoptotic cell death was determined using the TUNEL assay. Statistical Analysis Used: One- or two-way analysis of variance was deemed as appropriate, followed by relevant post t-test to determine P values. Results: The difference of MCF-7 cell death through increasing post-radiation time from 24 to 72 h following the dose of 1, 6 and 10 Gy was found to be 2%, 9.6% and 7.14%, respectively. D0of MCF-7 was 220 cGy and the SF in the cells irradiated by 1 Gy and 10 Gy doses were 0.8 and 0.0001, respectively. The estimated variances were 2%, 11.1% and 8.4%, between 24 h and 72 h post-radiation apoptosis death for 1, 6, and 10 Gy, respectively. Conclusions: The dose and time dependence inducing apoptotic death was significant (P = 0.001). The delayed mortality and apoptosis was observed in MCF-7 cell, but the variance of total cell death and apoptosis in 24 and 72 h post-radiation with 6 Gy was obviously more than that with other doses.</abstract><cop>India</cop><pub>Wolters Kluwer - Medknow Publications</pub><pmid>27146733</pmid><doi>10.4103/0019-509X.180862</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record>
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subjects Apoptosis
Apoptosis - radiation effects
Breast cancer
Breast Neoplasms - pathology
Breast Neoplasms - radiotherapy
Cancer therapies
Care and treatment
Colonies & territories
Deoxyribonucleic acid
DNA
Dose-response relationship
Dose-Response Relationship, Radiation
Efficiency
Female
Gamma Rays - therapeutic use
Humans
Laboratories
MCF-7 Cells
Methods
Mortality
Observations
Patient outcomes
Radiation therapy
Radiotherapy
Studies
title Evaluation of gamma radiation-induced cytotoxicity of breast cancer cells: Is there a time-dependent dose with high efficiency?
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