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HOTAIR Induces the Downregulation of miR-200 Family Members in Gastric Cancer Cell Lines
BACKGROUND: Gastric cancer is the fourth most common human malignancy and the second reason for cancer morbidity worldwide. LncRNA HOTAIR has recently emerged as a promoter of metastasis in various cancer types, including GC, through the EMT process. However, the exact mechanism of HOTAIR in promoti...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pasteur Institute of Iran
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784900/ https://www.ncbi.nlm.nih.gov/pubmed/34923813 http://dx.doi.org/10.52547/ibj.26.1.77 |
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author | Bossaghzadeh, Fatemeh Hajjari, Mohammadreza Sheikhi, Abdolkarim Salahshourifar, Iman Irani, Shiva |
author_facet | Bossaghzadeh, Fatemeh Hajjari, Mohammadreza Sheikhi, Abdolkarim Salahshourifar, Iman Irani, Shiva |
author_sort | Bossaghzadeh, Fatemeh |
collection | PubMed |
description | BACKGROUND: Gastric cancer is the fourth most common human malignancy and the second reason for cancer morbidity worldwide. LncRNA HOTAIR has recently emerged as a promoter of metastasis in various cancer types, including GC, through the EMT process. However, the exact mechanism of HOTAIR in promoting EMT is unknown. Aberrant expression of the miR-200 family has been linked to the occurrence and development of various types of malignant tumors. This study investigates the correlation between the HOTAIR and miR-200 family gene expression patterns in GC cell lines. We investigated the miR-200 and HOTAIR due to their common molecular features in the EMT process. METHODS: AGS and MKN45 cell lines were transfected with si-HOTAIR, along with a negative control. The effect of HOTAIR knockdown was also analyzed on cell viability and also on the expression of miR-200 family members, including miR-200a, -200b, and -200c, in cell lines using qRT-PCR. Statistical analysis was performed to find the potential correlation between the expression level of HOTAIR and miRs. RESULTS: Our results showed significant increased miR-200 family expression level in transfected AGS and MKN45 GC cells (fold changes > 2; p < 0.001). Moreover, a negative correlation was observed between HOTAIR and miR-200 expression levels in GC cell lines (p < 0.05). CONCLUSION: Our findings showed a significant association between miR-200 family and HOTAIR expression levels in GC cell lines. Taken together, the HOTAIR-miR-200 axis seems to play a vital role in human GC, suggesting a potential therapeutic target in future GC treatment. |
format | Online Article Text |
id | pubmed-8784900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Pasteur Institute of Iran |
record_format | MEDLINE/PubMed |
spelling | pubmed-87849002022-02-07 HOTAIR Induces the Downregulation of miR-200 Family Members in Gastric Cancer Cell Lines Bossaghzadeh, Fatemeh Hajjari, Mohammadreza Sheikhi, Abdolkarim Salahshourifar, Iman Irani, Shiva Iran Biomed J Full Length BACKGROUND: Gastric cancer is the fourth most common human malignancy and the second reason for cancer morbidity worldwide. LncRNA HOTAIR has recently emerged as a promoter of metastasis in various cancer types, including GC, through the EMT process. However, the exact mechanism of HOTAIR in promoting EMT is unknown. Aberrant expression of the miR-200 family has been linked to the occurrence and development of various types of malignant tumors. This study investigates the correlation between the HOTAIR and miR-200 family gene expression patterns in GC cell lines. We investigated the miR-200 and HOTAIR due to their common molecular features in the EMT process. METHODS: AGS and MKN45 cell lines were transfected with si-HOTAIR, along with a negative control. The effect of HOTAIR knockdown was also analyzed on cell viability and also on the expression of miR-200 family members, including miR-200a, -200b, and -200c, in cell lines using qRT-PCR. Statistical analysis was performed to find the potential correlation between the expression level of HOTAIR and miRs. RESULTS: Our results showed significant increased miR-200 family expression level in transfected AGS and MKN45 GC cells (fold changes > 2; p < 0.001). Moreover, a negative correlation was observed between HOTAIR and miR-200 expression levels in GC cell lines (p < 0.05). CONCLUSION: Our findings showed a significant association between miR-200 family and HOTAIR expression levels in GC cell lines. Taken together, the HOTAIR-miR-200 axis seems to play a vital role in human GC, suggesting a potential therapeutic target in future GC treatment. Pasteur Institute of Iran 2022-01 2021-12-20 /pmc/articles/PMC8784900/ /pubmed/34923813 http://dx.doi.org/10.52547/ibj.26.1.77 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Length Bossaghzadeh, Fatemeh Hajjari, Mohammadreza Sheikhi, Abdolkarim Salahshourifar, Iman Irani, Shiva HOTAIR Induces the Downregulation of miR-200 Family Members in Gastric Cancer Cell Lines |
title |
HOTAIR Induces the Downregulation of miR-200 Family Members in Gastric Cancer Cell Lines |
title_full |
HOTAIR Induces the Downregulation of miR-200 Family Members in Gastric Cancer Cell Lines |
title_fullStr |
HOTAIR Induces the Downregulation of miR-200 Family Members in Gastric Cancer Cell Lines |
title_full_unstemmed |
HOTAIR Induces the Downregulation of miR-200 Family Members in Gastric Cancer Cell Lines |
title_short |
HOTAIR Induces the Downregulation of miR-200 Family Members in Gastric Cancer Cell Lines |
title_sort | hotair induces the downregulation of mir-200 family members in gastric cancer cell lines |
topic | Full Length |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784900/ https://www.ncbi.nlm.nih.gov/pubmed/34923813 http://dx.doi.org/10.52547/ibj.26.1.77 |
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