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Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer

AIM: To establish a permanent piwi like RNA-mediated gene silencing 1 (PIWIL1) gene knockout in AGP01 gastric cancer cell line using CRISPR-Cas9 system and analyze phenotypic modifications as well as gene expression alterations. METHODS: CRISPR-Cas9 system used was purchased from Dharmacon GE Life S...

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Autores principales: Araújo, Taíssa, Khayat, André, Quintana, Luciana, Calcagno, Danielle, Mourão, Ronald, Modesto, Antônio, Paiva, Juliana, Lima, Adhara, Moreira, Fabiano, Oliveira, Edivaldo, Souza, Michel, Othman, Moneeb, Liehr, Thomas, Abdelhay, Eliana, Gomes, Renata, Santos, Sidney, Assumpção, Paulo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305533/
https://www.ncbi.nlm.nih.gov/pubmed/30598579
http://dx.doi.org/10.3748/wjg.v24.i47.5338
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author Araújo, Taíssa
Khayat, André
Quintana, Luciana
Calcagno, Danielle
Mourão, Ronald
Modesto, Antônio
Paiva, Juliana
Lima, Adhara
Moreira, Fabiano
Oliveira, Edivaldo
Souza, Michel
Othman, Moneeb
Liehr, Thomas
Abdelhay, Eliana
Gomes, Renata
Santos, Sidney
Assumpção, Paulo
author_facet Araújo, Taíssa
Khayat, André
Quintana, Luciana
Calcagno, Danielle
Mourão, Ronald
Modesto, Antônio
Paiva, Juliana
Lima, Adhara
Moreira, Fabiano
Oliveira, Edivaldo
Souza, Michel
Othman, Moneeb
Liehr, Thomas
Abdelhay, Eliana
Gomes, Renata
Santos, Sidney
Assumpção, Paulo
author_sort Araújo, Taíssa
collection PubMed
description AIM: To establish a permanent piwi like RNA-mediated gene silencing 1 (PIWIL1) gene knockout in AGP01 gastric cancer cell line using CRISPR-Cas9 system and analyze phenotypic modifications as well as gene expression alterations. METHODS: CRISPR-Cas9 system used was purchased from Dharmacon GE Life Sciences (Lafayette, CO, United States) and permanent knockout was performed according to manufacturer’s recommendations. Wound-healing assay was performed to investigate the effect of PIWIL1 knockout on migration capability of cells and Boyden chamber invasion assay was performed to investigate the effect on invasion capability. For the gene expression analysis, a one-color microarray-based gene expression analysis kit (Agilent Technologies, Santa Clara, CA, United States) was used according to the protocol provided by the manufacturer. RESULTS: PIWIL1 gene knockout caused a significant decrease in AGP01 migration capacity as well as a significant decrease in cell invasiveness. Moreover, functional analysis based on grouping of all differentially expressed mRNAs identified a total of 35 genes (5 up-regulated and 30 down-regulated) encoding proteins involved in cellular invasion and migration. According to current literature, 9 of these 35 genes (DOCK2, ZNF503, PDE4D, ABL1, ABL2, LPAR1, SMAD2, WASF3 and DACH1) are possibly related to the mechanisms used by PIWIL1 to promote carcinogenic effects related to migration and invasion, since their functions are consistent with the changes observed (being up- or down-regulated after knockout). CONCLUSION: Taken together, these data reinforce the idea that PIWIL1 plays a crucial role in the signaling pathway of gastric cancer, regulating several genes involved in migration and invasion processes; therefore, its use as a therapeutic target may generate promising results in the treatment of gastric cancer.
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spelling pubmed-63055332018-12-31 Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer Araújo, Taíssa Khayat, André Quintana, Luciana Calcagno, Danielle Mourão, Ronald Modesto, Antônio Paiva, Juliana Lima, Adhara Moreira, Fabiano Oliveira, Edivaldo Souza, Michel Othman, Moneeb Liehr, Thomas Abdelhay, Eliana Gomes, Renata Santos, Sidney Assumpção, Paulo World J Gastroenterol Basic Study AIM: To establish a permanent piwi like RNA-mediated gene silencing 1 (PIWIL1) gene knockout in AGP01 gastric cancer cell line using CRISPR-Cas9 system and analyze phenotypic modifications as well as gene expression alterations. METHODS: CRISPR-Cas9 system used was purchased from Dharmacon GE Life Sciences (Lafayette, CO, United States) and permanent knockout was performed according to manufacturer’s recommendations. Wound-healing assay was performed to investigate the effect of PIWIL1 knockout on migration capability of cells and Boyden chamber invasion assay was performed to investigate the effect on invasion capability. For the gene expression analysis, a one-color microarray-based gene expression analysis kit (Agilent Technologies, Santa Clara, CA, United States) was used according to the protocol provided by the manufacturer. RESULTS: PIWIL1 gene knockout caused a significant decrease in AGP01 migration capacity as well as a significant decrease in cell invasiveness. Moreover, functional analysis based on grouping of all differentially expressed mRNAs identified a total of 35 genes (5 up-regulated and 30 down-regulated) encoding proteins involved in cellular invasion and migration. According to current literature, 9 of these 35 genes (DOCK2, ZNF503, PDE4D, ABL1, ABL2, LPAR1, SMAD2, WASF3 and DACH1) are possibly related to the mechanisms used by PIWIL1 to promote carcinogenic effects related to migration and invasion, since their functions are consistent with the changes observed (being up- or down-regulated after knockout). CONCLUSION: Taken together, these data reinforce the idea that PIWIL1 plays a crucial role in the signaling pathway of gastric cancer, regulating several genes involved in migration and invasion processes; therefore, its use as a therapeutic target may generate promising results in the treatment of gastric cancer. Baishideng Publishing Group Inc 2018-12-21 2018-12-21 /pmc/articles/PMC6305533/ /pubmed/30598579 http://dx.doi.org/10.3748/wjg.v24.i47.5338 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Basic Study
Araújo, Taíssa
Khayat, André
Quintana, Luciana
Calcagno, Danielle
Mourão, Ronald
Modesto, Antônio
Paiva, Juliana
Lima, Adhara
Moreira, Fabiano
Oliveira, Edivaldo
Souza, Michel
Othman, Moneeb
Liehr, Thomas
Abdelhay, Eliana
Gomes, Renata
Santos, Sidney
Assumpção, Paulo
Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer
title Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer
title_full Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer
title_fullStr Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer
title_full_unstemmed Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer
title_short Piwi like RNA-mediated gene silencing 1 gene as a possible major player in gastric cancer
title_sort piwi like rna-mediated gene silencing 1 gene as a possible major player in gastric cancer
topic Basic Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305533/
https://www.ncbi.nlm.nih.gov/pubmed/30598579
http://dx.doi.org/10.3748/wjg.v24.i47.5338
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