Cargando…

Stem Extract from Momordica cochinchinensis Induces Apoptosis in Chemoresistant Human Prostate Cancer Cells (PC-3)

Natural compounds have been recognized as valuable sources for anticancer drug development. In this work, different parts from Momordica cochinchinensis Spreng were selected to perform cytotoxic screening against human prostate cancer (PC-3) cells. Chromatographic separation and purification were pe...

Descripción completa

Detalles Bibliográficos
Autores principales: Chainumnim, Seksom, Saenkham, Audchara, Dolsophon, Kulvadee, Chainok, Kittipong, Suksamrarn, Sunit, Tanechpongtamb, Wanlaya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878451/
https://www.ncbi.nlm.nih.gov/pubmed/35209099
http://dx.doi.org/10.3390/molecules27041313
_version_ 1784658663369080832
author Chainumnim, Seksom
Saenkham, Audchara
Dolsophon, Kulvadee
Chainok, Kittipong
Suksamrarn, Sunit
Tanechpongtamb, Wanlaya
author_facet Chainumnim, Seksom
Saenkham, Audchara
Dolsophon, Kulvadee
Chainok, Kittipong
Suksamrarn, Sunit
Tanechpongtamb, Wanlaya
author_sort Chainumnim, Seksom
collection PubMed
description Natural compounds have been recognized as valuable sources for anticancer drug development. In this work, different parts from Momordica cochinchinensis Spreng were selected to perform cytotoxic screening against human prostate cancer (PC-3) cells. Chromatographic separation and purification were performed for the main constituents of the most effective extract. The content of the fatty acids was determined by Gas Chromatography-Flame Ionization Detector (GC–FID). Chemical structural elucidation was performed by spectroscopic means. For the mechanism of the apoptotic induction of the most effective extract, the characteristics were evaluated by Hoechst 33342 staining, sub-G1 peak analysis, JC-1 staining, and Western blotting. As a result, extracts from different parts of M. cochinchinensis significantly inhibited cancer cell viability. The most effective stem extract induced apoptosis in PC-3 cells by causing nuclear fragmentation, increasing the sub-G1 peak, and changing the mitochondrial membrane potential. Additionally, the stem extract increased the pro-apoptotic (caspase-3 and Noxa) mediators while decreasing the anti-apoptotic (Bcl-xL and Mcl-1) mediators. The main constituents of the stem extract are α-spinasterol and ligballinol, as well as some fatty acids. Our results demonstrated that the stem extract of M. cochinchinensis has cytotoxic and apoptotic effects in PC-3 cells. These results provide basic knowledge for developing antiproliferative agents for prostate cancer in the future.
format Online
Article
Text
id pubmed-8878451
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-88784512022-02-26 Stem Extract from Momordica cochinchinensis Induces Apoptosis in Chemoresistant Human Prostate Cancer Cells (PC-3) Chainumnim, Seksom Saenkham, Audchara Dolsophon, Kulvadee Chainok, Kittipong Suksamrarn, Sunit Tanechpongtamb, Wanlaya Molecules Article Natural compounds have been recognized as valuable sources for anticancer drug development. In this work, different parts from Momordica cochinchinensis Spreng were selected to perform cytotoxic screening against human prostate cancer (PC-3) cells. Chromatographic separation and purification were performed for the main constituents of the most effective extract. The content of the fatty acids was determined by Gas Chromatography-Flame Ionization Detector (GC–FID). Chemical structural elucidation was performed by spectroscopic means. For the mechanism of the apoptotic induction of the most effective extract, the characteristics were evaluated by Hoechst 33342 staining, sub-G1 peak analysis, JC-1 staining, and Western blotting. As a result, extracts from different parts of M. cochinchinensis significantly inhibited cancer cell viability. The most effective stem extract induced apoptosis in PC-3 cells by causing nuclear fragmentation, increasing the sub-G1 peak, and changing the mitochondrial membrane potential. Additionally, the stem extract increased the pro-apoptotic (caspase-3 and Noxa) mediators while decreasing the anti-apoptotic (Bcl-xL and Mcl-1) mediators. The main constituents of the stem extract are α-spinasterol and ligballinol, as well as some fatty acids. Our results demonstrated that the stem extract of M. cochinchinensis has cytotoxic and apoptotic effects in PC-3 cells. These results provide basic knowledge for developing antiproliferative agents for prostate cancer in the future. MDPI 2022-02-15 /pmc/articles/PMC8878451/ /pubmed/35209099 http://dx.doi.org/10.3390/molecules27041313 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chainumnim, Seksom
Saenkham, Audchara
Dolsophon, Kulvadee
Chainok, Kittipong
Suksamrarn, Sunit
Tanechpongtamb, Wanlaya
Stem Extract from Momordica cochinchinensis Induces Apoptosis in Chemoresistant Human Prostate Cancer Cells (PC-3)
title Stem Extract from Momordica cochinchinensis Induces Apoptosis in Chemoresistant Human Prostate Cancer Cells (PC-3)
title_full Stem Extract from Momordica cochinchinensis Induces Apoptosis in Chemoresistant Human Prostate Cancer Cells (PC-3)
title_fullStr Stem Extract from Momordica cochinchinensis Induces Apoptosis in Chemoresistant Human Prostate Cancer Cells (PC-3)
title_full_unstemmed Stem Extract from Momordica cochinchinensis Induces Apoptosis in Chemoresistant Human Prostate Cancer Cells (PC-3)
title_short Stem Extract from Momordica cochinchinensis Induces Apoptosis in Chemoresistant Human Prostate Cancer Cells (PC-3)
title_sort stem extract from momordica cochinchinensis induces apoptosis in chemoresistant human prostate cancer cells (pc-3)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878451/
https://www.ncbi.nlm.nih.gov/pubmed/35209099
http://dx.doi.org/10.3390/molecules27041313
work_keys_str_mv AT chainumnimseksom stemextractfrommomordicacochinchinensisinducesapoptosisinchemoresistanthumanprostatecancercellspc3
AT saenkhamaudchara stemextractfrommomordicacochinchinensisinducesapoptosisinchemoresistanthumanprostatecancercellspc3
AT dolsophonkulvadee stemextractfrommomordicacochinchinensisinducesapoptosisinchemoresistanthumanprostatecancercellspc3
AT chainokkittipong stemextractfrommomordicacochinchinensisinducesapoptosisinchemoresistanthumanprostatecancercellspc3
AT suksamrarnsunit stemextractfrommomordicacochinchinensisinducesapoptosisinchemoresistanthumanprostatecancercellspc3
AT tanechpongtambwanlaya stemextractfrommomordicacochinchinensisinducesapoptosisinchemoresistanthumanprostatecancercellspc3