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Hsa-let-7d-5p Promotes Gastric Cancer Progression by Targeting PRDM5

Gastric cancer (GC) is a common malignant tumor in the digestive system and a significant health burden worldwide. In this study, we found that hsa-let-7d-5p was upregulated in GC cells, promoted GC cell proliferation, migration, and invasion, and reduced apoptosis. Moreover, we found that the expre...

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Autores principales: Gao, Xiang, Liu, Huiqi, Wang, Rong, Huang, Mingyu, Wu, Qiong, Wang, Yang, Zhang, Wei, Liu, Yongnian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283079/
https://www.ncbi.nlm.nih.gov/pubmed/35847370
http://dx.doi.org/10.1155/2022/2700651
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author Gao, Xiang
Liu, Huiqi
Wang, Rong
Huang, Mingyu
Wu, Qiong
Wang, Yang
Zhang, Wei
Liu, Yongnian
author_facet Gao, Xiang
Liu, Huiqi
Wang, Rong
Huang, Mingyu
Wu, Qiong
Wang, Yang
Zhang, Wei
Liu, Yongnian
author_sort Gao, Xiang
collection PubMed
description Gastric cancer (GC) is a common malignant tumor in the digestive system and a significant health burden worldwide. In this study, we found that hsa-let-7d-5p was upregulated in GC cells, promoted GC cell proliferation, migration, and invasion, and reduced apoptosis. Moreover, we found that the expression of PRDM5 (PR domain protein 5) was downregulated in GC cells and upregulated in GC cells treated with hsa-let-7d-5p inhibitor. Further investigation showed that hsa-let-7d-5p was the target of PRDM5, and the functions of hsa-let-7d-5p on GC progression were rescued by PRDM5 overexpression in GC cells. Collectively, our findings suggested that hsa-let-7d-5p promoted the development of GC by targeting PRDM5, indicating that hsa-let-7d-5p could be a promising therapeutic molecule for the treatment of gastric cancer.
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spelling pubmed-92830792022-07-15 Hsa-let-7d-5p Promotes Gastric Cancer Progression by Targeting PRDM5 Gao, Xiang Liu, Huiqi Wang, Rong Huang, Mingyu Wu, Qiong Wang, Yang Zhang, Wei Liu, Yongnian J Oncol Research Article Gastric cancer (GC) is a common malignant tumor in the digestive system and a significant health burden worldwide. In this study, we found that hsa-let-7d-5p was upregulated in GC cells, promoted GC cell proliferation, migration, and invasion, and reduced apoptosis. Moreover, we found that the expression of PRDM5 (PR domain protein 5) was downregulated in GC cells and upregulated in GC cells treated with hsa-let-7d-5p inhibitor. Further investigation showed that hsa-let-7d-5p was the target of PRDM5, and the functions of hsa-let-7d-5p on GC progression were rescued by PRDM5 overexpression in GC cells. Collectively, our findings suggested that hsa-let-7d-5p promoted the development of GC by targeting PRDM5, indicating that hsa-let-7d-5p could be a promising therapeutic molecule for the treatment of gastric cancer. Hindawi 2022-07-07 /pmc/articles/PMC9283079/ /pubmed/35847370 http://dx.doi.org/10.1155/2022/2700651 Text en Copyright © 2022 Xiang Gao et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gao, Xiang
Liu, Huiqi
Wang, Rong
Huang, Mingyu
Wu, Qiong
Wang, Yang
Zhang, Wei
Liu, Yongnian
Hsa-let-7d-5p Promotes Gastric Cancer Progression by Targeting PRDM5
title Hsa-let-7d-5p Promotes Gastric Cancer Progression by Targeting PRDM5
title_full Hsa-let-7d-5p Promotes Gastric Cancer Progression by Targeting PRDM5
title_fullStr Hsa-let-7d-5p Promotes Gastric Cancer Progression by Targeting PRDM5
title_full_unstemmed Hsa-let-7d-5p Promotes Gastric Cancer Progression by Targeting PRDM5
title_short Hsa-let-7d-5p Promotes Gastric Cancer Progression by Targeting PRDM5
title_sort hsa-let-7d-5p promotes gastric cancer progression by targeting prdm5
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283079/
https://www.ncbi.nlm.nih.gov/pubmed/35847370
http://dx.doi.org/10.1155/2022/2700651
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