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Flavonoid Calycopterin Induces Apoptosis in Human Prostate Cancer Cells In-vitro
Prostate cancer is enumerated as one of the most prevalent cancers in men, with a mortality rate of 18%. Chemotherapy is considered as a common strategy for cancer treatment; however, toxic side effects and drug resistance associated with chemotherapy are major drawbacks with this approach. It is we...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shaheed Beheshti University of Medical Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7758012/ https://www.ncbi.nlm.nih.gov/pubmed/33680039 http://dx.doi.org/10.22037/ijpr.2020.113410.14283 |
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author | Lotfizadeh, Reza Sepehri, Houri Attari, Farnoosh Delphi, Ladan |
author_facet | Lotfizadeh, Reza Sepehri, Houri Attari, Farnoosh Delphi, Ladan |
author_sort | Lotfizadeh, Reza |
collection | PubMed |
description | Prostate cancer is enumerated as one of the most prevalent cancers in men, with a mortality rate of 18%. Chemotherapy is considered as a common strategy for cancer treatment; however, toxic side effects and drug resistance associated with chemotherapy are major drawbacks with this approach. It is well known that a diet rich in flavonoids can reduce the incidence of many types of cancer in a significant manner, and it was proved that methoxy flavones have greater bioavailability compared to the nonmethylated ones. Calycopterin is a tetramethoxy flavone which was demonstrated to have anti-proliferative effects on colon, gastric, and osteosarcoma cancer cells. Therefore, in the current study, we have evaluated the apoptotic effects of this flavonoid on two prostate cancer cell lines in-vitro. The MTT assay revealed that after 48 h treatment with this flavonoid, cell viability reduced to 50% compared to the control group. However, calycopterin treatment of healthy HUVEC did not cause any significant reduction in cell viability. Moreover, the clonogenic assay demonstrated that after 14 days, colony size and numbers reduced significantly in calycopterin treated cells. In addition, the percentage of the sub-G1 population in calycopterin-treated cells augmented significantly compared to untreated group. Also, calycopterin-treated cells demonstrated shiny condensed nuclei with fragmented DNA indicative of apoptosis. Finally, a significant reduction in the migration ability was observed in both lines subjected to calycopterin after 48 h. To conclude, our results demonstrated the apoptotic and anti-metastatic effects of calycopterin in both hormone-dependent and independent prostate cancer cell lines. |
format | Online Article Text |
id | pubmed-7758012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Shaheed Beheshti University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-77580122021-03-05 Flavonoid Calycopterin Induces Apoptosis in Human Prostate Cancer Cells In-vitro Lotfizadeh, Reza Sepehri, Houri Attari, Farnoosh Delphi, Ladan Iran J Pharm Res Original Article Prostate cancer is enumerated as one of the most prevalent cancers in men, with a mortality rate of 18%. Chemotherapy is considered as a common strategy for cancer treatment; however, toxic side effects and drug resistance associated with chemotherapy are major drawbacks with this approach. It is well known that a diet rich in flavonoids can reduce the incidence of many types of cancer in a significant manner, and it was proved that methoxy flavones have greater bioavailability compared to the nonmethylated ones. Calycopterin is a tetramethoxy flavone which was demonstrated to have anti-proliferative effects on colon, gastric, and osteosarcoma cancer cells. Therefore, in the current study, we have evaluated the apoptotic effects of this flavonoid on two prostate cancer cell lines in-vitro. The MTT assay revealed that after 48 h treatment with this flavonoid, cell viability reduced to 50% compared to the control group. However, calycopterin treatment of healthy HUVEC did not cause any significant reduction in cell viability. Moreover, the clonogenic assay demonstrated that after 14 days, colony size and numbers reduced significantly in calycopterin treated cells. In addition, the percentage of the sub-G1 population in calycopterin-treated cells augmented significantly compared to untreated group. Also, calycopterin-treated cells demonstrated shiny condensed nuclei with fragmented DNA indicative of apoptosis. Finally, a significant reduction in the migration ability was observed in both lines subjected to calycopterin after 48 h. To conclude, our results demonstrated the apoptotic and anti-metastatic effects of calycopterin in both hormone-dependent and independent prostate cancer cell lines. Shaheed Beheshti University of Medical Sciences 2020 /pmc/articles/PMC7758012/ /pubmed/33680039 http://dx.doi.org/10.22037/ijpr.2020.113410.14283 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lotfizadeh, Reza Sepehri, Houri Attari, Farnoosh Delphi, Ladan Flavonoid Calycopterin Induces Apoptosis in Human Prostate Cancer Cells In-vitro |
title | Flavonoid Calycopterin Induces Apoptosis in Human Prostate Cancer Cells In-vitro |
title_full | Flavonoid Calycopterin Induces Apoptosis in Human Prostate Cancer Cells In-vitro |
title_fullStr | Flavonoid Calycopterin Induces Apoptosis in Human Prostate Cancer Cells In-vitro |
title_full_unstemmed | Flavonoid Calycopterin Induces Apoptosis in Human Prostate Cancer Cells In-vitro |
title_short | Flavonoid Calycopterin Induces Apoptosis in Human Prostate Cancer Cells In-vitro |
title_sort | flavonoid calycopterin induces apoptosis in human prostate cancer cells in-vitro |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7758012/ https://www.ncbi.nlm.nih.gov/pubmed/33680039 http://dx.doi.org/10.22037/ijpr.2020.113410.14283 |
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