Dark Sweet Cherry (<i>Prunus avium</i>) Anthocyanins Suppressed ERK1/2-Akt/mTOR Cell Signaling and Oxidative Stress: Implications for TNBC Growth and Invasion

This study aimed to assess dark sweet cherry (DSC) total polyphenols (WE) and anthocyanins (ACN) against metastatic breast cancer (BC). The WE and ACN anticancer activity and underlying mechanisms were assessed in vitro using 4T1 BC cells. A pilot study using a BALB/C mouse syngeneic model bearing 4...

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Main Authors: Ana Carolina Silveira Rabelo, Susanne U. Mertens-Talcott, Boon P. Chew, Giuliana Noratto
Format: Article
Language:English
Published: MDPI AG 2022-10-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/27/21/7245
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author Ana Carolina Silveira Rabelo
Susanne U. Mertens-Talcott
Boon P. Chew
Giuliana Noratto
author_facet Ana Carolina Silveira Rabelo
Susanne U. Mertens-Talcott
Boon P. Chew
Giuliana Noratto
author_sort Ana Carolina Silveira Rabelo
collection DOAJ
description This study aimed to assess dark sweet cherry (DSC) total polyphenols (WE) and anthocyanins (ACN) against metastatic breast cancer (BC). The WE and ACN anticancer activity and underlying mechanisms were assessed in vitro using 4T1 BC cells. A pilot study using a BALB/C mouse syngeneic model bearing 4T1 tumors assessed the anti-metastatic potential of ACN in vivo. ACN inhibited cell viability with higher potency than WE and reduced reactive oxygen species (ROS) (IC<sub>50</sub> = 58.6 µg cyanidin 3-glucoside equivalent (C3G)/mL or 122 µM). ACN induced p38 stress-related intrinsic apoptosis, leading to caspase-3 cleavage and total PARP decrease. ACN suppressed ERK1/2 and Akt/mTOR signaling pathways, which are abnormally activated in BC and promote motility and invasion. This was consistent with suppression of VCAM-1 mRNA, Scr phosphorylation and 88.6% reduction of cells migrating to wounded area. The pilot in vivo results supported the ACN-mediated suppression of angiogenesis in tumors and lungs. ACN also lowered Cenpf mRNA in lungs, associated with lung metastasis lesions and poor survival. Results demonstrated the dual Akt-ERK inhibitory role of ACN and suppression of their downstream pro-invasive targets. These results encourage a larger scale in vivo study to confirm that ACN may help to fight BC invasion and metastasis.
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spelling doaj.art-acd5a84f35144a6a8552aed785dacfb02023-11-24T06:01:02ZengMDPI AGMolecules1420-30492022-10-012721724510.3390/molecules27217245Dark Sweet Cherry (<i>Prunus avium</i>) Anthocyanins Suppressed ERK1/2-Akt/mTOR Cell Signaling and Oxidative Stress: Implications for TNBC Growth and InvasionAna Carolina Silveira Rabelo0Susanne U. Mertens-Talcott1Boon P. Chew2Giuliana Noratto3Department of Food and Experimental Nutrition, Faculty of Pharmaceutical Sciences, University of São Paulo, São Paulo 05508 270, BrazilDepartment of Food Science and Technology, Texas A&M University, College Station, TX 77843-2253, USADepartment of Food Science and Technology, Texas A&M University, College Station, TX 77843-2253, USADepartment of Food Science and Technology, Texas A&M University, College Station, TX 77843-2253, USAThis study aimed to assess dark sweet cherry (DSC) total polyphenols (WE) and anthocyanins (ACN) against metastatic breast cancer (BC). The WE and ACN anticancer activity and underlying mechanisms were assessed in vitro using 4T1 BC cells. A pilot study using a BALB/C mouse syngeneic model bearing 4T1 tumors assessed the anti-metastatic potential of ACN in vivo. ACN inhibited cell viability with higher potency than WE and reduced reactive oxygen species (ROS) (IC<sub>50</sub> = 58.6 µg cyanidin 3-glucoside equivalent (C3G)/mL or 122 µM). ACN induced p38 stress-related intrinsic apoptosis, leading to caspase-3 cleavage and total PARP decrease. ACN suppressed ERK1/2 and Akt/mTOR signaling pathways, which are abnormally activated in BC and promote motility and invasion. This was consistent with suppression of VCAM-1 mRNA, Scr phosphorylation and 88.6% reduction of cells migrating to wounded area. The pilot in vivo results supported the ACN-mediated suppression of angiogenesis in tumors and lungs. ACN also lowered Cenpf mRNA in lungs, associated with lung metastasis lesions and poor survival. Results demonstrated the dual Akt-ERK inhibitory role of ACN and suppression of their downstream pro-invasive targets. These results encourage a larger scale in vivo study to confirm that ACN may help to fight BC invasion and metastasis.https://www.mdpi.com/1420-3049/27/21/72454T1-CRL-2539anthocyaninsdark sweet cherriespolyphenolsmetastasisangiogenesis
spellingShingle Ana Carolina Silveira Rabelo
Susanne U. Mertens-Talcott
Boon P. Chew
Giuliana Noratto
Dark Sweet Cherry (<i>Prunus avium</i>) Anthocyanins Suppressed ERK1/2-Akt/mTOR Cell Signaling and Oxidative Stress: Implications for TNBC Growth and Invasion
Molecules
4T1-CRL-2539
anthocyanins
dark sweet cherries
polyphenols
metastasis
angiogenesis
title Dark Sweet Cherry (<i>Prunus avium</i>) Anthocyanins Suppressed ERK1/2-Akt/mTOR Cell Signaling and Oxidative Stress: Implications for TNBC Growth and Invasion
title_full Dark Sweet Cherry (<i>Prunus avium</i>) Anthocyanins Suppressed ERK1/2-Akt/mTOR Cell Signaling and Oxidative Stress: Implications for TNBC Growth and Invasion
title_fullStr Dark Sweet Cherry (<i>Prunus avium</i>) Anthocyanins Suppressed ERK1/2-Akt/mTOR Cell Signaling and Oxidative Stress: Implications for TNBC Growth and Invasion
title_full_unstemmed Dark Sweet Cherry (<i>Prunus avium</i>) Anthocyanins Suppressed ERK1/2-Akt/mTOR Cell Signaling and Oxidative Stress: Implications for TNBC Growth and Invasion
title_short Dark Sweet Cherry (<i>Prunus avium</i>) Anthocyanins Suppressed ERK1/2-Akt/mTOR Cell Signaling and Oxidative Stress: Implications for TNBC Growth and Invasion
title_sort dark sweet cherry i prunus avium i anthocyanins suppressed erk1 2 akt mtor cell signaling and oxidative stress implications for tnbc growth and invasion
topic 4T1-CRL-2539
anthocyanins
dark sweet cherries
polyphenols
metastasis
angiogenesis
url https://www.mdpi.com/1420-3049/27/21/7245
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