Proteomic Analysis of the Protective Effect of Eriodictyol on Benzo(a)pyrene-Induced Caco-2 Cytotoxicity

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Proteomic Analysis of the Protective Effect of Eriodictyol on Benzo(a)pyrene-Induced Caco-2 Cytotoxicity. / Wang, Chong; Zhao, Fan; Bai, Yun; Li, Chunbao; Xu, Xinglian; Kristiansen, Karsten; Zhou, Guanghong.

In: Frontiers in Nutrition, Vol. 9, 839364, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Wang, C, Zhao, F, Bai, Y, Li, C, Xu, X, Kristiansen, K & Zhou, G 2022, 'Proteomic Analysis of the Protective Effect of Eriodictyol on Benzo(a)pyrene-Induced Caco-2 Cytotoxicity', Frontiers in Nutrition, vol. 9, 839364. https://doi.org/10.3389/fnut.2022.839364

APA

Wang, C., Zhao, F., Bai, Y., Li, C., Xu, X., Kristiansen, K., & Zhou, G. (2022). Proteomic Analysis of the Protective Effect of Eriodictyol on Benzo(a)pyrene-Induced Caco-2 Cytotoxicity. Frontiers in Nutrition, 9, [839364]. https://doi.org/10.3389/fnut.2022.839364

Vancouver

Wang C, Zhao F, Bai Y, Li C, Xu X, Kristiansen K et al. Proteomic Analysis of the Protective Effect of Eriodictyol on Benzo(a)pyrene-Induced Caco-2 Cytotoxicity. Frontiers in Nutrition. 2022;9. 839364. https://doi.org/10.3389/fnut.2022.839364

Author

Wang, Chong ; Zhao, Fan ; Bai, Yun ; Li, Chunbao ; Xu, Xinglian ; Kristiansen, Karsten ; Zhou, Guanghong. / Proteomic Analysis of the Protective Effect of Eriodictyol on Benzo(a)pyrene-Induced Caco-2 Cytotoxicity. In: Frontiers in Nutrition. 2022 ; Vol. 9.

Bibtex

@article{40a9c99d1e2a4216b1e9242648955fbc,
title = "Proteomic Analysis of the Protective Effect of Eriodictyol on Benzo(a)pyrene-Induced Caco-2 Cytotoxicity",
abstract = "We evaluated the possible protective effects of six polyphenols on benzo(a)pyrene (BaP)-induced cytotoxicity in Caco-2 cells. We show that treatment with quinic acid, ferulic acid, homovanillic acid, trolox and BaP decreased cell viability, whereas naringenin and eriodictyol affected viability in a bi-phasic manner with low concentrations decreasing viability whereas higher concentrations increase viability. Co-treatment with 20 μM eriodictyol or naringenin reduced BaP-induced cytotoxicity, including cell apoptosis, cell cycle progression, and oxidative stress. Our results show that the protective effect of eriodictyol was superior to that of naringenin. The potential protective mechanisms of eriodictyol on BaP-induced toxicity were investigated by proteomics. We identified 80 differentially expressed proteins (DEPs) with proteins associated with genetic information processing pathway representing the highest proportion and number of proteins responding to eriodictyol treatment, including key proteins such as RPA2, SNRPA, RAD23B, NUP155 and AARS. Our results provide new knowledge on how polyphenols may prevent BaP-induced carcinogenesis.",
author = "Chong Wang and Fan Zhao and Yun Bai and Chunbao Li and Xinglian Xu and Karsten Kristiansen and Guanghong Zhou",
note = "Copyright {\textcopyright} 2022 Wang, Zhao, Bai, Li, Xu, Kristiansen and Zhou.",
year = "2022",
doi = "10.3389/fnut.2022.839364",
language = "English",
volume = "9",
journal = "Frontiers in Nutrition",
issn = "2296-861X",
publisher = "Frontiers",

}

RIS

TY - JOUR

T1 - Proteomic Analysis of the Protective Effect of Eriodictyol on Benzo(a)pyrene-Induced Caco-2 Cytotoxicity

AU - Wang, Chong

AU - Zhao, Fan

AU - Bai, Yun

AU - Li, Chunbao

AU - Xu, Xinglian

AU - Kristiansen, Karsten

AU - Zhou, Guanghong

N1 - Copyright © 2022 Wang, Zhao, Bai, Li, Xu, Kristiansen and Zhou.

PY - 2022

Y1 - 2022

N2 - We evaluated the possible protective effects of six polyphenols on benzo(a)pyrene (BaP)-induced cytotoxicity in Caco-2 cells. We show that treatment with quinic acid, ferulic acid, homovanillic acid, trolox and BaP decreased cell viability, whereas naringenin and eriodictyol affected viability in a bi-phasic manner with low concentrations decreasing viability whereas higher concentrations increase viability. Co-treatment with 20 μM eriodictyol or naringenin reduced BaP-induced cytotoxicity, including cell apoptosis, cell cycle progression, and oxidative stress. Our results show that the protective effect of eriodictyol was superior to that of naringenin. The potential protective mechanisms of eriodictyol on BaP-induced toxicity were investigated by proteomics. We identified 80 differentially expressed proteins (DEPs) with proteins associated with genetic information processing pathway representing the highest proportion and number of proteins responding to eriodictyol treatment, including key proteins such as RPA2, SNRPA, RAD23B, NUP155 and AARS. Our results provide new knowledge on how polyphenols may prevent BaP-induced carcinogenesis.

AB - We evaluated the possible protective effects of six polyphenols on benzo(a)pyrene (BaP)-induced cytotoxicity in Caco-2 cells. We show that treatment with quinic acid, ferulic acid, homovanillic acid, trolox and BaP decreased cell viability, whereas naringenin and eriodictyol affected viability in a bi-phasic manner with low concentrations decreasing viability whereas higher concentrations increase viability. Co-treatment with 20 μM eriodictyol or naringenin reduced BaP-induced cytotoxicity, including cell apoptosis, cell cycle progression, and oxidative stress. Our results show that the protective effect of eriodictyol was superior to that of naringenin. The potential protective mechanisms of eriodictyol on BaP-induced toxicity were investigated by proteomics. We identified 80 differentially expressed proteins (DEPs) with proteins associated with genetic information processing pathway representing the highest proportion and number of proteins responding to eriodictyol treatment, including key proteins such as RPA2, SNRPA, RAD23B, NUP155 and AARS. Our results provide new knowledge on how polyphenols may prevent BaP-induced carcinogenesis.

U2 - 10.3389/fnut.2022.839364

DO - 10.3389/fnut.2022.839364

M3 - Journal article

C2 - 35308267

VL - 9

JO - Frontiers in Nutrition

JF - Frontiers in Nutrition

SN - 2296-861X

M1 - 839364

ER -

ID: 307754170