Cargando…

Serum Eicosanoids Metabolomics Profile in a Mouse Model of Renal Cell Carcinoma: Predicting the Antitumor Efficacy of Anlotinib

Anlotinib (ANL) shows promising efficacy in patients with renal cell cancer (RCC). Here, for the first time, a serum eicosanoid metabolomics profile and pharmacodynamics in Renca syngeneic mice treated with ANL was performed and integrated using our previous HPLC-MS/MS method and multivariate statis...

Descripción completa

Detalles Bibliográficos
Autores principales: Du, Ping, Xuan, Lingling, Hu, Ting, An, Zhuoling, Liu, Lihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863591/
https://www.ncbi.nlm.nih.gov/pubmed/35222406
http://dx.doi.org/10.3389/fimmu.2022.824607
_version_ 1784655268234133504
author Du, Ping
Xuan, Lingling
Hu, Ting
An, Zhuoling
Liu, Lihong
author_facet Du, Ping
Xuan, Lingling
Hu, Ting
An, Zhuoling
Liu, Lihong
author_sort Du, Ping
collection PubMed
description Anlotinib (ANL) shows promising efficacy in patients with renal cell cancer (RCC). Here, for the first time, a serum eicosanoid metabolomics profile and pharmacodynamics in Renca syngeneic mice treated with ANL was performed and integrated using our previous HPLC-MS/MS method and multivariate statistical analysis. The tumor growth inhibition rates of ANL were 39% and 52% at low (3 mg/kg) and high (6 mg/kg) dose levels, without obvious toxicity. A total of 15 disturbed metabolites were observed between the normal group and the model group, and the intrinsic metabolic phenotype alterations had occurred due to the treatment of ANL. A total of eight potential metabolites from the refined partial least squares (PLS) model were considered as potential predictive biomarkers for the efficacy of ANL, and the DHA held the most outstanding sensitivity and specificity with an area under the receiver operating characteristic curve of 0.88. Collectively, the results of this exploratory study not only provide a powerful reference for understanding eicosanoid metabolic reprogramming of ANL but also offer an innovative perspective for the development of therapeutic targets and strategies, the discovery of predictive biomarkers, and the determination of effective tumor monitoring approaches.
format Online
Article
Text
id pubmed-8863591
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-88635912022-02-24 Serum Eicosanoids Metabolomics Profile in a Mouse Model of Renal Cell Carcinoma: Predicting the Antitumor Efficacy of Anlotinib Du, Ping Xuan, Lingling Hu, Ting An, Zhuoling Liu, Lihong Front Immunol Immunology Anlotinib (ANL) shows promising efficacy in patients with renal cell cancer (RCC). Here, for the first time, a serum eicosanoid metabolomics profile and pharmacodynamics in Renca syngeneic mice treated with ANL was performed and integrated using our previous HPLC-MS/MS method and multivariate statistical analysis. The tumor growth inhibition rates of ANL were 39% and 52% at low (3 mg/kg) and high (6 mg/kg) dose levels, without obvious toxicity. A total of 15 disturbed metabolites were observed between the normal group and the model group, and the intrinsic metabolic phenotype alterations had occurred due to the treatment of ANL. A total of eight potential metabolites from the refined partial least squares (PLS) model were considered as potential predictive biomarkers for the efficacy of ANL, and the DHA held the most outstanding sensitivity and specificity with an area under the receiver operating characteristic curve of 0.88. Collectively, the results of this exploratory study not only provide a powerful reference for understanding eicosanoid metabolic reprogramming of ANL but also offer an innovative perspective for the development of therapeutic targets and strategies, the discovery of predictive biomarkers, and the determination of effective tumor monitoring approaches. Frontiers Media S.A. 2022-02-09 /pmc/articles/PMC8863591/ /pubmed/35222406 http://dx.doi.org/10.3389/fimmu.2022.824607 Text en Copyright © 2022 Du, Xuan, Hu, An and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Du, Ping
Xuan, Lingling
Hu, Ting
An, Zhuoling
Liu, Lihong
Serum Eicosanoids Metabolomics Profile in a Mouse Model of Renal Cell Carcinoma: Predicting the Antitumor Efficacy of Anlotinib
title Serum Eicosanoids Metabolomics Profile in a Mouse Model of Renal Cell Carcinoma: Predicting the Antitumor Efficacy of Anlotinib
title_full Serum Eicosanoids Metabolomics Profile in a Mouse Model of Renal Cell Carcinoma: Predicting the Antitumor Efficacy of Anlotinib
title_fullStr Serum Eicosanoids Metabolomics Profile in a Mouse Model of Renal Cell Carcinoma: Predicting the Antitumor Efficacy of Anlotinib
title_full_unstemmed Serum Eicosanoids Metabolomics Profile in a Mouse Model of Renal Cell Carcinoma: Predicting the Antitumor Efficacy of Anlotinib
title_short Serum Eicosanoids Metabolomics Profile in a Mouse Model of Renal Cell Carcinoma: Predicting the Antitumor Efficacy of Anlotinib
title_sort serum eicosanoids metabolomics profile in a mouse model of renal cell carcinoma: predicting the antitumor efficacy of anlotinib
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863591/
https://www.ncbi.nlm.nih.gov/pubmed/35222406
http://dx.doi.org/10.3389/fimmu.2022.824607
work_keys_str_mv AT duping serumeicosanoidsmetabolomicsprofileinamousemodelofrenalcellcarcinomapredictingtheantitumorefficacyofanlotinib
AT xuanlingling serumeicosanoidsmetabolomicsprofileinamousemodelofrenalcellcarcinomapredictingtheantitumorefficacyofanlotinib
AT huting serumeicosanoidsmetabolomicsprofileinamousemodelofrenalcellcarcinomapredictingtheantitumorefficacyofanlotinib
AT anzhuoling serumeicosanoidsmetabolomicsprofileinamousemodelofrenalcellcarcinomapredictingtheantitumorefficacyofanlotinib
AT liulihong serumeicosanoidsmetabolomicsprofileinamousemodelofrenalcellcarcinomapredictingtheantitumorefficacyofanlotinib