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Small molecules related to adrenomedullin reduce tumor burden in a mouse model of colitis-associated colon cancer

To investigate the contribution of adrenomedullin (AM) and its gene-related peptide, proadrenomedullin N-terminal 20 peptide (PAMP), to the progression and potential treatment of colon cancer we studied the effects of four small molecules (SM) related to AM and PAMP on a mouse model of colon cancer....

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Autores principales: Ochoa-Callejero, Laura, García-Sanmartín, Josune, Martínez-Herrero, Sonia, Rubio-Mediavilla, Susana, Narro-Íñiguez, Judit, Martínez, Alfredo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727507/
https://www.ncbi.nlm.nih.gov/pubmed/29235493
http://dx.doi.org/10.1038/s41598-017-17573-x
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author Ochoa-Callejero, Laura
García-Sanmartín, Josune
Martínez-Herrero, Sonia
Rubio-Mediavilla, Susana
Narro-Íñiguez, Judit
Martínez, Alfredo
author_facet Ochoa-Callejero, Laura
García-Sanmartín, Josune
Martínez-Herrero, Sonia
Rubio-Mediavilla, Susana
Narro-Íñiguez, Judit
Martínez, Alfredo
author_sort Ochoa-Callejero, Laura
collection PubMed
description To investigate the contribution of adrenomedullin (AM) and its gene-related peptide, proadrenomedullin N-terminal 20 peptide (PAMP), to the progression and potential treatment of colon cancer we studied the effects of four small molecules (SM) related to AM and PAMP on a mouse model of colon cancer. For each SM, four experimental groups of male mice were used: (i) Control group; (ii) SM group; (iii) DSS group (injected with azoxymethane [AOM] and drank dextran sulfate sodium [DSS]); and (iv) DSS + SM group (treated with AOM, DSS, and the SM). None of the mice in groups i and ii developed tumors, whereas all mice in groups iii and iv developed colon neoplasias. No significant differences were found among mice treated with PAMP modulators (87877 and 106221). Mice that received the AM negative modulator, 16311, had worse colitis symptoms than their control counterparts, whereas mice injected with the AM positive modulator, 145425, had a lower number of tumors than their controls. SM 145425 regulated the expression of proliferation marker Lgr5 and had an impact on microbiota, preventing the DSS-elicited increase of the Bacteroides/Prevotella ratio. These results suggest that treatment with AM or with positive modulator SMs may represent a novel strategy for colon cancer.
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spelling pubmed-57275072017-12-18 Small molecules related to adrenomedullin reduce tumor burden in a mouse model of colitis-associated colon cancer Ochoa-Callejero, Laura García-Sanmartín, Josune Martínez-Herrero, Sonia Rubio-Mediavilla, Susana Narro-Íñiguez, Judit Martínez, Alfredo Sci Rep Article To investigate the contribution of adrenomedullin (AM) and its gene-related peptide, proadrenomedullin N-terminal 20 peptide (PAMP), to the progression and potential treatment of colon cancer we studied the effects of four small molecules (SM) related to AM and PAMP on a mouse model of colon cancer. For each SM, four experimental groups of male mice were used: (i) Control group; (ii) SM group; (iii) DSS group (injected with azoxymethane [AOM] and drank dextran sulfate sodium [DSS]); and (iv) DSS + SM group (treated with AOM, DSS, and the SM). None of the mice in groups i and ii developed tumors, whereas all mice in groups iii and iv developed colon neoplasias. No significant differences were found among mice treated with PAMP modulators (87877 and 106221). Mice that received the AM negative modulator, 16311, had worse colitis symptoms than their control counterparts, whereas mice injected with the AM positive modulator, 145425, had a lower number of tumors than their controls. SM 145425 regulated the expression of proliferation marker Lgr5 and had an impact on microbiota, preventing the DSS-elicited increase of the Bacteroides/Prevotella ratio. These results suggest that treatment with AM or with positive modulator SMs may represent a novel strategy for colon cancer. Nature Publishing Group UK 2017-12-13 /pmc/articles/PMC5727507/ /pubmed/29235493 http://dx.doi.org/10.1038/s41598-017-17573-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ochoa-Callejero, Laura
García-Sanmartín, Josune
Martínez-Herrero, Sonia
Rubio-Mediavilla, Susana
Narro-Íñiguez, Judit
Martínez, Alfredo
Small molecules related to adrenomedullin reduce tumor burden in a mouse model of colitis-associated colon cancer
title Small molecules related to adrenomedullin reduce tumor burden in a mouse model of colitis-associated colon cancer
title_full Small molecules related to adrenomedullin reduce tumor burden in a mouse model of colitis-associated colon cancer
title_fullStr Small molecules related to adrenomedullin reduce tumor burden in a mouse model of colitis-associated colon cancer
title_full_unstemmed Small molecules related to adrenomedullin reduce tumor burden in a mouse model of colitis-associated colon cancer
title_short Small molecules related to adrenomedullin reduce tumor burden in a mouse model of colitis-associated colon cancer
title_sort small molecules related to adrenomedullin reduce tumor burden in a mouse model of colitis-associated colon cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727507/
https://www.ncbi.nlm.nih.gov/pubmed/29235493
http://dx.doi.org/10.1038/s41598-017-17573-x
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