Anacardic Acids from <i>Amphipterygium adstringens</i> Confer Cytoprotection against 5-Fluorouracil and Carboplatin Induced Blood Cell Toxicity While Increasing Antitumoral Activity and Survival in an Animal Model of Breast Cancer

<i>Amphipterygium adstringens</i> (cuachalalate) contains anacardic acids (AAs) such as 6-pentadecyl salicylic acid (6SA) that show immunomodulatory and antitumor activity with minimal or no secondary adverse effects. By contrast, most chemotherapeutic agents, such as 5-fluorouracil (5-F...

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Main Authors: Jairo Galot-Linaldi, Karla M. Hernández-Sánchez, Elizabet Estrada-Muñiz, Libia Vega
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/11/3241
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spelling doaj-5bacc1243d1f4ad0a5e2b6b37720185d2021-06-01T01:26:20ZengMDPI AGMolecules1420-30492021-05-01263241324110.3390/molecules26113241Anacardic Acids from <i>Amphipterygium adstringens</i> Confer Cytoprotection against 5-Fluorouracil and Carboplatin Induced Blood Cell Toxicity While Increasing Antitumoral Activity and Survival in an Animal Model of Breast CancerJairo Galot-Linaldi0Karla M. Hernández-Sánchez1Elizabet Estrada-Muñiz2Libia Vega3Department of Toxicology, Center for Research and Advanced Studies of the National Polytechnic Institute, Ave. IPN 2508, San Pedro Zacatenco, GA Madero, Mexico City 07360, MexicoEscuela Nacional de Ciencias Biológicas del Instituto Politécnico Nacional, Prolongación de Carpio y Plan de Ayala s/n, Santo Tómas, Miguel Hidalgo, Mexico City 11340, MexicoDepartment of Toxicology, Center for Research and Advanced Studies of the National Polytechnic Institute, Ave. IPN 2508, San Pedro Zacatenco, GA Madero, Mexico City 07360, MexicoDepartment of Toxicology, Center for Research and Advanced Studies of the National Polytechnic Institute, Ave. IPN 2508, San Pedro Zacatenco, GA Madero, Mexico City 07360, Mexico<i>Amphipterygium adstringens</i> (cuachalalate) contains anacardic acids (AAs) such as 6-pentadecyl salicylic acid (6SA) that show immunomodulatory and antitumor activity with minimal or no secondary adverse effects. By contrast, most chemotherapeutic agents, such as 5-fluorouracil (5-FU) and carboplatin (CbPt), induce myelosuppression and leukopenia. Here, we investigated the myeloprotective and antineoplastic potential of an AA extract or the 6SA as monotherapy or in combination with commonly used chemotherapeutic agents (5-FU and CbPt) to determine the cytoprotective action of 6SA on immune cells. Treatment of Balb/c breast tumor-bearing female mice with an AA mixture or 6SA did not induce the myelosuppression or leukopenia observed with 5-FU and CbPt. The co-administration of AA mixture or isolated 6SA with 5-FU or CbPt reduced the apoptosis of circulating blood cells and bone marrow cells. Treatment of 4T1 breast tumor-bearing mice with the AA mixture or 6SA reduced tumor growth and lung metastasis and increased the survival rate compared with monotherapies. An increased effect was observed in tumor reduction with the combination of 6SA and CbPt. In conclusion, AAs have important myeloprotective and antineoplastic effects, and they can improve the efficiency of chemotherapeutics, thereby protecting the organism against the toxic effects of drugs such as 5-FU and CbPt.https://www.mdpi.com/1420-3049/26/11/3241<i>Amphiterygium adstringens</i>anacardic acidsmyeloprotectiveantineoplastic agentautologous tumor model
collection DOAJ
language English
format Article
sources DOAJ
author Jairo Galot-Linaldi
Karla M. Hernández-Sánchez
Elizabet Estrada-Muñiz
Libia Vega
spellingShingle Jairo Galot-Linaldi
Karla M. Hernández-Sánchez
Elizabet Estrada-Muñiz
Libia Vega
Anacardic Acids from <i>Amphipterygium adstringens</i> Confer Cytoprotection against 5-Fluorouracil and Carboplatin Induced Blood Cell Toxicity While Increasing Antitumoral Activity and Survival in an Animal Model of Breast Cancer
Molecules
<i>Amphiterygium adstringens</i>
anacardic acids
myeloprotective
antineoplastic agent
autologous tumor model
author_facet Jairo Galot-Linaldi
Karla M. Hernández-Sánchez
Elizabet Estrada-Muñiz
Libia Vega
author_sort Jairo Galot-Linaldi
title Anacardic Acids from <i>Amphipterygium adstringens</i> Confer Cytoprotection against 5-Fluorouracil and Carboplatin Induced Blood Cell Toxicity While Increasing Antitumoral Activity and Survival in an Animal Model of Breast Cancer
title_short Anacardic Acids from <i>Amphipterygium adstringens</i> Confer Cytoprotection against 5-Fluorouracil and Carboplatin Induced Blood Cell Toxicity While Increasing Antitumoral Activity and Survival in an Animal Model of Breast Cancer
title_full Anacardic Acids from <i>Amphipterygium adstringens</i> Confer Cytoprotection against 5-Fluorouracil and Carboplatin Induced Blood Cell Toxicity While Increasing Antitumoral Activity and Survival in an Animal Model of Breast Cancer
title_fullStr Anacardic Acids from <i>Amphipterygium adstringens</i> Confer Cytoprotection against 5-Fluorouracil and Carboplatin Induced Blood Cell Toxicity While Increasing Antitumoral Activity and Survival in an Animal Model of Breast Cancer
title_full_unstemmed Anacardic Acids from <i>Amphipterygium adstringens</i> Confer Cytoprotection against 5-Fluorouracil and Carboplatin Induced Blood Cell Toxicity While Increasing Antitumoral Activity and Survival in an Animal Model of Breast Cancer
title_sort anacardic acids from <i>amphipterygium adstringens</i> confer cytoprotection against 5-fluorouracil and carboplatin induced blood cell toxicity while increasing antitumoral activity and survival in an animal model of breast cancer
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2021-05-01
description <i>Amphipterygium adstringens</i> (cuachalalate) contains anacardic acids (AAs) such as 6-pentadecyl salicylic acid (6SA) that show immunomodulatory and antitumor activity with minimal or no secondary adverse effects. By contrast, most chemotherapeutic agents, such as 5-fluorouracil (5-FU) and carboplatin (CbPt), induce myelosuppression and leukopenia. Here, we investigated the myeloprotective and antineoplastic potential of an AA extract or the 6SA as monotherapy or in combination with commonly used chemotherapeutic agents (5-FU and CbPt) to determine the cytoprotective action of 6SA on immune cells. Treatment of Balb/c breast tumor-bearing female mice with an AA mixture or 6SA did not induce the myelosuppression or leukopenia observed with 5-FU and CbPt. The co-administration of AA mixture or isolated 6SA with 5-FU or CbPt reduced the apoptosis of circulating blood cells and bone marrow cells. Treatment of 4T1 breast tumor-bearing mice with the AA mixture or 6SA reduced tumor growth and lung metastasis and increased the survival rate compared with monotherapies. An increased effect was observed in tumor reduction with the combination of 6SA and CbPt. In conclusion, AAs have important myeloprotective and antineoplastic effects, and they can improve the efficiency of chemotherapeutics, thereby protecting the organism against the toxic effects of drugs such as 5-FU and CbPt.
topic <i>Amphiterygium adstringens</i>
anacardic acids
myeloprotective
antineoplastic agent
autologous tumor model
url https://www.mdpi.com/1420-3049/26/11/3241
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