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miR-196a Is Able to Restore the Aggressive Phenotype of Annexin A1 Knock-Out in Pancreatic Cancer Cells by CRISPR/Cas9 Genome Editing

Annexin A1 (ANXA1) is a Ca(2+)-binding protein that is involved in pancreatic cancer (PC) progression. It is able to mediate cytoskeletal organization maintaining a malignant phenotype. Our previous studies showed that ANXA1 Knock-Out (KO) MIA PaCa-2 cells partially lost their migratory and invasive...

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Autores principales: Belvedere, Raffaella, Saggese, Pasquale, Pessolano, Emanuela, Memoli, Domenico, Bizzarro, Valentina, Rizzo, Francesca, Parente, Luca, Weisz, Alessandro, Petrella, Antonello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073506/
https://www.ncbi.nlm.nih.gov/pubmed/29986379
http://dx.doi.org/10.3390/ijms19071967
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author Belvedere, Raffaella
Saggese, Pasquale
Pessolano, Emanuela
Memoli, Domenico
Bizzarro, Valentina
Rizzo, Francesca
Parente, Luca
Weisz, Alessandro
Petrella, Antonello
author_facet Belvedere, Raffaella
Saggese, Pasquale
Pessolano, Emanuela
Memoli, Domenico
Bizzarro, Valentina
Rizzo, Francesca
Parente, Luca
Weisz, Alessandro
Petrella, Antonello
author_sort Belvedere, Raffaella
collection PubMed
description Annexin A1 (ANXA1) is a Ca(2+)-binding protein that is involved in pancreatic cancer (PC) progression. It is able to mediate cytoskeletal organization maintaining a malignant phenotype. Our previous studies showed that ANXA1 Knock-Out (KO) MIA PaCa-2 cells partially lost their migratory and invasive capabilities and also the metastatization process appeared affected in vivo. Here, we investigated the microRNA (miRNA) profile in ANXA1 KO cells finding that the modification in miRNA expression suggests the significant involvement of ANXA1 in PC development. In this study, we focused on miR-196a which appeared down modulated in absence of ANXA1. This miRNA is a well known oncogenic factor in several tumour models and it is able to trigger the agents of the epithelial to mesenchymal transition (EMT), like ANXA1. Our results show that the reintroduction in ANXA1 KO cells of miR-196a through the mimic sequence restored the early aggressive phenotype of MIA PaCa-2. Then, ANXA1 seems to support the expression of miR-196a and its role. On the other hand, this miRNA is able to mediate cytoskeletal dynamics and other protein functions promoting PC cell migration and invasion. This work describes the correlation between ANXA1 and specific miRNA sequences, particularly miR-196a. These results could lead to further information on ANXA1 intracellular role in PC, explaining other aspects that are apart from its tumorigenic behaviour.
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spelling pubmed-60735062018-08-13 miR-196a Is Able to Restore the Aggressive Phenotype of Annexin A1 Knock-Out in Pancreatic Cancer Cells by CRISPR/Cas9 Genome Editing Belvedere, Raffaella Saggese, Pasquale Pessolano, Emanuela Memoli, Domenico Bizzarro, Valentina Rizzo, Francesca Parente, Luca Weisz, Alessandro Petrella, Antonello Int J Mol Sci Article Annexin A1 (ANXA1) is a Ca(2+)-binding protein that is involved in pancreatic cancer (PC) progression. It is able to mediate cytoskeletal organization maintaining a malignant phenotype. Our previous studies showed that ANXA1 Knock-Out (KO) MIA PaCa-2 cells partially lost their migratory and invasive capabilities and also the metastatization process appeared affected in vivo. Here, we investigated the microRNA (miRNA) profile in ANXA1 KO cells finding that the modification in miRNA expression suggests the significant involvement of ANXA1 in PC development. In this study, we focused on miR-196a which appeared down modulated in absence of ANXA1. This miRNA is a well known oncogenic factor in several tumour models and it is able to trigger the agents of the epithelial to mesenchymal transition (EMT), like ANXA1. Our results show that the reintroduction in ANXA1 KO cells of miR-196a through the mimic sequence restored the early aggressive phenotype of MIA PaCa-2. Then, ANXA1 seems to support the expression of miR-196a and its role. On the other hand, this miRNA is able to mediate cytoskeletal dynamics and other protein functions promoting PC cell migration and invasion. This work describes the correlation between ANXA1 and specific miRNA sequences, particularly miR-196a. These results could lead to further information on ANXA1 intracellular role in PC, explaining other aspects that are apart from its tumorigenic behaviour. MDPI 2018-07-06 /pmc/articles/PMC6073506/ /pubmed/29986379 http://dx.doi.org/10.3390/ijms19071967 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Belvedere, Raffaella
Saggese, Pasquale
Pessolano, Emanuela
Memoli, Domenico
Bizzarro, Valentina
Rizzo, Francesca
Parente, Luca
Weisz, Alessandro
Petrella, Antonello
miR-196a Is Able to Restore the Aggressive Phenotype of Annexin A1 Knock-Out in Pancreatic Cancer Cells by CRISPR/Cas9 Genome Editing
title miR-196a Is Able to Restore the Aggressive Phenotype of Annexin A1 Knock-Out in Pancreatic Cancer Cells by CRISPR/Cas9 Genome Editing
title_full miR-196a Is Able to Restore the Aggressive Phenotype of Annexin A1 Knock-Out in Pancreatic Cancer Cells by CRISPR/Cas9 Genome Editing
title_fullStr miR-196a Is Able to Restore the Aggressive Phenotype of Annexin A1 Knock-Out in Pancreatic Cancer Cells by CRISPR/Cas9 Genome Editing
title_full_unstemmed miR-196a Is Able to Restore the Aggressive Phenotype of Annexin A1 Knock-Out in Pancreatic Cancer Cells by CRISPR/Cas9 Genome Editing
title_short miR-196a Is Able to Restore the Aggressive Phenotype of Annexin A1 Knock-Out in Pancreatic Cancer Cells by CRISPR/Cas9 Genome Editing
title_sort mir-196a is able to restore the aggressive phenotype of annexin a1 knock-out in pancreatic cancer cells by crispr/cas9 genome editing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073506/
https://www.ncbi.nlm.nih.gov/pubmed/29986379
http://dx.doi.org/10.3390/ijms19071967
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