Crab Shell Extract Induces Prostate Cancer Cell Line (LNcap) Apoptosis and Decreases Nitric Oxide Secretion
Objective Prostate cancer is the second most common cancer worldwide. Chemotherapeutic agents have been shown to have adverse side-effects, and natural compounds have been recommended for cancer treatment, nowadays. Crab shell has been shown to have cancer preventative and suppressive effects in vi...
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2017-04-01
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doaj-a5b8801d5d474b96abe04747466132072020-11-25T01:49:00ZengRoyan Institute (ACECR), TehranCell Journal2228-58062228-58142017-04-0119223123710.22074/cellj.2017.4879Crab Shell Extract Induces Prostate Cancer Cell Line (LNcap) Apoptosis and Decreases Nitric Oxide Secretion Leila Rezakhani0Mohammad Rasool Khazaei1Ali Ghanbari2Mozafar Khazaei3Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, IranFertility and Infertility Research Center, Kermanshah University of Medical Sciences, Kermanshah, IranFertility and Infertility Research Center, Kermanshah University of Medical Sciences, Kermanshah, IranFertility and Infertility Research Center, Kermanshah University of Medical Sciences, Kermanshah, IranObjective Prostate cancer is the second most common cancer worldwide. Chemotherapeutic agents have been shown to have adverse side-effects, and natural compounds have been recommended for cancer treatment, nowadays. Crab shell has been shown to have cancer preventative and suppressive effects in vivo and in vitro. The aim of present study was to investigate the effect of crab shell extract on prostate cancer cell line (LNcap) in vitro. Materials and Methods In this in vitro experimental study, LNcap cells were treated with different concentrations (0, 100, 200, 400, 800 and 1000 µg/ml) of crab shell hydroalcoholic extract in three different culture periods (24, 48 and 72 hours). LNcap viability was evaluated by trypan blue staining and MTT assay. Cell apoptosis and nitric oxide (NO) secretion were determined by TUNEL and Griess assays, respectively. Data were analyzed by one-way ANOVA test and P<0.05 was considered significant. Results LNcap viability was decreased dose- and time-dependently. Thus 400, 800, and 1000 µg/ml doses showed significant differences compared to control group (P<0.001). Dose-dependent increase in the apoptotic index was also observed in 800 and 1000 µg/ ml concentrations (P<0.001). Nitric oxide secretion of LNcap cell was decreased time- and dose-dependently, while it was significant for 1000 µg/ml (P<0.05). Conclusion Crab shell extract showed anti-prostate cancer effect, by inducing cell apop- tosis and decreasing NO production. http://celljournal.org/journal/article/10418/downloadApoptosisCell survivalProstate Cancer |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Leila Rezakhani Mohammad Rasool Khazaei Ali Ghanbari Mozafar Khazaei |
spellingShingle |
Leila Rezakhani Mohammad Rasool Khazaei Ali Ghanbari Mozafar Khazaei Crab Shell Extract Induces Prostate Cancer Cell Line (LNcap) Apoptosis and Decreases Nitric Oxide Secretion Cell Journal Apoptosis Cell survival Prostate Cancer |
author_facet |
Leila Rezakhani Mohammad Rasool Khazaei Ali Ghanbari Mozafar Khazaei |
author_sort |
Leila Rezakhani |
title |
Crab Shell Extract Induces Prostate Cancer Cell Line (LNcap) Apoptosis and Decreases Nitric Oxide Secretion |
title_short |
Crab Shell Extract Induces Prostate Cancer Cell Line (LNcap) Apoptosis and Decreases Nitric Oxide Secretion |
title_full |
Crab Shell Extract Induces Prostate Cancer Cell Line (LNcap) Apoptosis and Decreases Nitric Oxide Secretion |
title_fullStr |
Crab Shell Extract Induces Prostate Cancer Cell Line (LNcap) Apoptosis and Decreases Nitric Oxide Secretion |
title_full_unstemmed |
Crab Shell Extract Induces Prostate Cancer Cell Line (LNcap) Apoptosis and Decreases Nitric Oxide Secretion |
title_sort |
crab shell extract induces prostate cancer cell line (lncap) apoptosis and decreases nitric oxide secretion |
publisher |
Royan Institute (ACECR), Tehran |
series |
Cell Journal |
issn |
2228-5806 2228-5814 |
publishDate |
2017-04-01 |
description |
Objective
Prostate cancer is the second most common cancer worldwide. Chemotherapeutic agents have been shown to have adverse side-effects, and natural compounds have been recommended for cancer treatment, nowadays. Crab shell has been shown to have cancer preventative and suppressive effects in vivo and in vitro. The aim of present study was to investigate the effect of crab shell extract on prostate cancer cell line (LNcap) in vitro.
Materials and Methods
In this in vitro experimental study, LNcap cells were treated with different concentrations (0, 100, 200, 400, 800 and 1000 µg/ml) of crab shell hydroalcoholic extract in three different culture periods (24, 48 and 72 hours). LNcap viability was evaluated by trypan blue staining and MTT assay. Cell apoptosis and nitric oxide (NO) secretion were determined by TUNEL and Griess assays, respectively. Data were analyzed by one-way ANOVA test and P<0.05 was considered significant.
Results
LNcap viability was decreased dose- and time-dependently. Thus 400, 800, and 1000 µg/ml doses showed significant differences compared to control group (P<0.001). Dose-dependent increase in the apoptotic index was also observed in 800 and 1000 µg/ ml concentrations (P<0.001). Nitric oxide secretion of LNcap cell was decreased time- and dose-dependently, while it was significant for 1000 µg/ml (P<0.05).
Conclusion
Crab shell extract showed anti-prostate cancer effect, by inducing cell apop- tosis and decreasing NO production.
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topic |
Apoptosis Cell survival Prostate Cancer |
url |
http://celljournal.org/journal/article/10418/download |
work_keys_str_mv |
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