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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2018
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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. |
format | Online Article Text |
id | pubmed-6305533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
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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