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Antiproliferative and apoptotic effect of Morus nigra extract on human prostate cancer cells

Background: Morus nigra L. belongs to the family Moraceae and is frequently used in traditional medicine. Numerous studies have investigated the antiproliferative effects of various extracts of different Morus species, but studies involving the in vitro cytotoxic effect of M. nigra extract are very...

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Autores principales: Turan, Ibrahim, Demir, Selim, Kilinc, Kagan, Burnaz, Nesibe Arslan, Yaman, Serap Ozer, Akbulut, Kubra, Mentese, Ahmet, Aliyazicioglu, Yuksel, Deger, Orhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355563/
https://www.ncbi.nlm.nih.gov/pubmed/28344475
http://dx.doi.org/10.1016/j.jsps.2016.06.002
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author Turan, Ibrahim
Demir, Selim
Kilinc, Kagan
Burnaz, Nesibe Arslan
Yaman, Serap Ozer
Akbulut, Kubra
Mentese, Ahmet
Aliyazicioglu, Yuksel
Deger, Orhan
author_facet Turan, Ibrahim
Demir, Selim
Kilinc, Kagan
Burnaz, Nesibe Arslan
Yaman, Serap Ozer
Akbulut, Kubra
Mentese, Ahmet
Aliyazicioglu, Yuksel
Deger, Orhan
author_sort Turan, Ibrahim
collection PubMed
description Background: Morus nigra L. belongs to the family Moraceae and is frequently used in traditional medicine. Numerous studies have investigated the antiproliferative effects of various extracts of different Morus species, but studies involving the in vitro cytotoxic effect of M. nigra extract are very limited. The purpose of this study was to evaluate the phenolic composition and antioxidant activity of dimethyl sulfoxide extract of M. nigra (DEM) and to investigate, for the first time, the probable cytotoxic effect in human prostate adenocarcinoma (PC-3) cells together with the mechanism involved. Methods: Total polyphenolic contents (TPC), ferric reducing antioxidant power (FRAP) and phenolic compounds of DEM were evaluated using spectrophotometric procedures and HPLC. The cytotoxic effect of DEM on PC-3 cells was revealed using the MTT assay. Mechanisms involved in the cytotoxic effect of DEM on PC-3 cells were then investigated in terms of apoptosis, mitochondrial membrane potential and cell cycle using flow cytometry, while caspase activity was investigated using luminometric analysis. Results: TPC and FRAP values were 20.7 ± 0.3 mg gallic acid equivalents and 48.8 ± 1.6 mg trolox equivalents per g sample, respectively. Ascorbic acid and chlorogenic acid were the major phenolic compounds detected at HPLC analysis. DEM arrested the cell cycle of PC-3 cells at the G(1) phase, induced apoptosis via increased caspase activity and reduced mitochondrial membrane potential. Conclusions: Our results indicate that M. nigra may be a novel candidate for the development of new natural product based therapeutic agents against prostate cancer.
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spelling pubmed-53555632017-03-24 Antiproliferative and apoptotic effect of Morus nigra extract on human prostate cancer cells Turan, Ibrahim Demir, Selim Kilinc, Kagan Burnaz, Nesibe Arslan Yaman, Serap Ozer Akbulut, Kubra Mentese, Ahmet Aliyazicioglu, Yuksel Deger, Orhan Saudi Pharm J Original Article Background: Morus nigra L. belongs to the family Moraceae and is frequently used in traditional medicine. Numerous studies have investigated the antiproliferative effects of various extracts of different Morus species, but studies involving the in vitro cytotoxic effect of M. nigra extract are very limited. The purpose of this study was to evaluate the phenolic composition and antioxidant activity of dimethyl sulfoxide extract of M. nigra (DEM) and to investigate, for the first time, the probable cytotoxic effect in human prostate adenocarcinoma (PC-3) cells together with the mechanism involved. Methods: Total polyphenolic contents (TPC), ferric reducing antioxidant power (FRAP) and phenolic compounds of DEM were evaluated using spectrophotometric procedures and HPLC. The cytotoxic effect of DEM on PC-3 cells was revealed using the MTT assay. Mechanisms involved in the cytotoxic effect of DEM on PC-3 cells were then investigated in terms of apoptosis, mitochondrial membrane potential and cell cycle using flow cytometry, while caspase activity was investigated using luminometric analysis. Results: TPC and FRAP values were 20.7 ± 0.3 mg gallic acid equivalents and 48.8 ± 1.6 mg trolox equivalents per g sample, respectively. Ascorbic acid and chlorogenic acid were the major phenolic compounds detected at HPLC analysis. DEM arrested the cell cycle of PC-3 cells at the G(1) phase, induced apoptosis via increased caspase activity and reduced mitochondrial membrane potential. Conclusions: Our results indicate that M. nigra may be a novel candidate for the development of new natural product based therapeutic agents against prostate cancer. Elsevier 2017-02 2016-06-20 /pmc/articles/PMC5355563/ /pubmed/28344475 http://dx.doi.org/10.1016/j.jsps.2016.06.002 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Turan, Ibrahim
Demir, Selim
Kilinc, Kagan
Burnaz, Nesibe Arslan
Yaman, Serap Ozer
Akbulut, Kubra
Mentese, Ahmet
Aliyazicioglu, Yuksel
Deger, Orhan
Antiproliferative and apoptotic effect of Morus nigra extract on human prostate cancer cells
title Antiproliferative and apoptotic effect of Morus nigra extract on human prostate cancer cells
title_full Antiproliferative and apoptotic effect of Morus nigra extract on human prostate cancer cells
title_fullStr Antiproliferative and apoptotic effect of Morus nigra extract on human prostate cancer cells
title_full_unstemmed Antiproliferative and apoptotic effect of Morus nigra extract on human prostate cancer cells
title_short Antiproliferative and apoptotic effect of Morus nigra extract on human prostate cancer cells
title_sort antiproliferative and apoptotic effect of morus nigra extract on human prostate cancer cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355563/
https://www.ncbi.nlm.nih.gov/pubmed/28344475
http://dx.doi.org/10.1016/j.jsps.2016.06.002
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