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Proteome Analysis of the Antiproliferative Activity of the Novel Chitooligosaccharide–Gallic Acid Conjugate against the SW620 Colon Cancer Cell Line

Chitooligosaccharide (COS) and gallic acid (GA) are natural compounds with anti-cancer properties, and their conjugate (COS–GA) has several biological activities. Herein, the anti-cancer activity of COS–GA in SW620 colon cancer cells was investigated. MTT assay was used to evaluate cell viability af...

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Autores principales: Saetang, Jirakrit, Sukkapat, Phutthipong, Mittal, Ajay, Julamanee, Jakrawadee, Khopanlert, Wannakorn, Maneechai, Kajornkiat, Nazeer, Rasool Abdul, Sangkhathat, Surasak, Benjakul, Soottawat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296375/
https://www.ncbi.nlm.nih.gov/pubmed/37371778
http://dx.doi.org/10.3390/biomedicines11061683
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author Saetang, Jirakrit
Sukkapat, Phutthipong
Mittal, Ajay
Julamanee, Jakrawadee
Khopanlert, Wannakorn
Maneechai, Kajornkiat
Nazeer, Rasool Abdul
Sangkhathat, Surasak
Benjakul, Soottawat
author_facet Saetang, Jirakrit
Sukkapat, Phutthipong
Mittal, Ajay
Julamanee, Jakrawadee
Khopanlert, Wannakorn
Maneechai, Kajornkiat
Nazeer, Rasool Abdul
Sangkhathat, Surasak
Benjakul, Soottawat
author_sort Saetang, Jirakrit
collection PubMed
description Chitooligosaccharide (COS) and gallic acid (GA) are natural compounds with anti-cancer properties, and their conjugate (COS–GA) has several biological activities. Herein, the anti-cancer activity of COS–GA in SW620 colon cancer cells was investigated. MTT assay was used to evaluate cell viability after treatment with 62.5, 122, and 250 µg/mL of COS, GA, and COS–GA for 24 and 48 h. The number of apoptotic cells was determined using flow cytometry. Proteomic analysis was used to explore the mechanisms of action of different compounds. COS–GA and GA showed a stronger anti-cancer effect than COS by reducing SW620 cell proliferation at 125 and 250 µg/mL within 24 h. Flow cytometry revealed 20% apoptosis after COS–GA treatment for 24 h. Thus, GA majorly contributed to the enhanced anti-cancer activity of COS via conjugation. Proteomic analysis revealed alterations in protein translation and DNA duplication in the COS group and the structural constituents of the cytoskeleton, intermediate filament organization, the mitochondrial nucleoid, and glycolytic processes in the COS–GA group. Anti-cancer-activity-related proteins were altered, including CLTA, HSPA9, HIST2H2BF, KRT18, HINT1, DSP, and VIM. Overall, the COS–GA conjugate can serve as a potential anti-cancer agent for the safe and effective treatment of colon cancer.
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spelling pubmed-102963752023-06-28 Proteome Analysis of the Antiproliferative Activity of the Novel Chitooligosaccharide–Gallic Acid Conjugate against the SW620 Colon Cancer Cell Line Saetang, Jirakrit Sukkapat, Phutthipong Mittal, Ajay Julamanee, Jakrawadee Khopanlert, Wannakorn Maneechai, Kajornkiat Nazeer, Rasool Abdul Sangkhathat, Surasak Benjakul, Soottawat Biomedicines Article Chitooligosaccharide (COS) and gallic acid (GA) are natural compounds with anti-cancer properties, and their conjugate (COS–GA) has several biological activities. Herein, the anti-cancer activity of COS–GA in SW620 colon cancer cells was investigated. MTT assay was used to evaluate cell viability after treatment with 62.5, 122, and 250 µg/mL of COS, GA, and COS–GA for 24 and 48 h. The number of apoptotic cells was determined using flow cytometry. Proteomic analysis was used to explore the mechanisms of action of different compounds. COS–GA and GA showed a stronger anti-cancer effect than COS by reducing SW620 cell proliferation at 125 and 250 µg/mL within 24 h. Flow cytometry revealed 20% apoptosis after COS–GA treatment for 24 h. Thus, GA majorly contributed to the enhanced anti-cancer activity of COS via conjugation. Proteomic analysis revealed alterations in protein translation and DNA duplication in the COS group and the structural constituents of the cytoskeleton, intermediate filament organization, the mitochondrial nucleoid, and glycolytic processes in the COS–GA group. Anti-cancer-activity-related proteins were altered, including CLTA, HSPA9, HIST2H2BF, KRT18, HINT1, DSP, and VIM. Overall, the COS–GA conjugate can serve as a potential anti-cancer agent for the safe and effective treatment of colon cancer. MDPI 2023-06-10 /pmc/articles/PMC10296375/ /pubmed/37371778 http://dx.doi.org/10.3390/biomedicines11061683 Text en © 2023 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
Saetang, Jirakrit
Sukkapat, Phutthipong
Mittal, Ajay
Julamanee, Jakrawadee
Khopanlert, Wannakorn
Maneechai, Kajornkiat
Nazeer, Rasool Abdul
Sangkhathat, Surasak
Benjakul, Soottawat
Proteome Analysis of the Antiproliferative Activity of the Novel Chitooligosaccharide–Gallic Acid Conjugate against the SW620 Colon Cancer Cell Line
title Proteome Analysis of the Antiproliferative Activity of the Novel Chitooligosaccharide–Gallic Acid Conjugate against the SW620 Colon Cancer Cell Line
title_full Proteome Analysis of the Antiproliferative Activity of the Novel Chitooligosaccharide–Gallic Acid Conjugate against the SW620 Colon Cancer Cell Line
title_fullStr Proteome Analysis of the Antiproliferative Activity of the Novel Chitooligosaccharide–Gallic Acid Conjugate against the SW620 Colon Cancer Cell Line
title_full_unstemmed Proteome Analysis of the Antiproliferative Activity of the Novel Chitooligosaccharide–Gallic Acid Conjugate against the SW620 Colon Cancer Cell Line
title_short Proteome Analysis of the Antiproliferative Activity of the Novel Chitooligosaccharide–Gallic Acid Conjugate against the SW620 Colon Cancer Cell Line
title_sort proteome analysis of the antiproliferative activity of the novel chitooligosaccharide–gallic acid conjugate against the sw620 colon cancer cell line
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296375/
https://www.ncbi.nlm.nih.gov/pubmed/37371778
http://dx.doi.org/10.3390/biomedicines11061683
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