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ELK1 Enhances Pancreatic Cancer Progression Via LGMN and Correlates with Poor Prognosis
Pancreatic cancer is one of the most lethal cancers and its prognosis is extremely poor. Clarification of molecular mechanisms and identification of prognostic biomarkers are urgently needed. Though we previously found that LGMN was involved in pancreatic carcinoma progression, the upstream regulati...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711721/ https://www.ncbi.nlm.nih.gov/pubmed/34966781 http://dx.doi.org/10.3389/fmolb.2021.764900 |
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author | Yan, Qiang Ni, Chenming Lin, Yingying Sun, Xu Shen, Zhenhua Zhang, Minjie Han, Shuwen Shi, Jiemin Mao, Jing Yang, Zhe Wang, Weilin |
author_facet | Yan, Qiang Ni, Chenming Lin, Yingying Sun, Xu Shen, Zhenhua Zhang, Minjie Han, Shuwen Shi, Jiemin Mao, Jing Yang, Zhe Wang, Weilin |
author_sort | Yan, Qiang |
collection | PubMed |
description | Pancreatic cancer is one of the most lethal cancers and its prognosis is extremely poor. Clarification of molecular mechanisms and identification of prognostic biomarkers are urgently needed. Though we previously found that LGMN was involved in pancreatic carcinoma progression, the upstream regulation of LGMN remains unknown. We used reliable software to search for the potential transcription factors that may be related with LGMN transcription, we found that ELK1 could be a new regulator of LGMN transcription that binded directly to the LGMN promoter. Moreover, knocking down of ELK1 reduced pancreatic cancer cells proliferation, invasion and survival, while LGMN restored the malignancy of pancreatic cancer in vitro and in vivo. Overexpression of ELK1 further increased cancer cells proliferation, invasion and survival. Clinically, ELK1 and LGMN were positively correlated with clinical stage, degree of differentiation and Lymph node infiltration. ELK1 and LGMN were identified as independent prognostic factors for overall survival. The patients with low expression of ELK1/LGMN survived an average of 29.65 months, whereas those with high expression of ELK1/LGMN survived an average of 16.67 months. In conclusive, our results revealed a new mechanism by which ELK1 promoted the progression of pancreatic cancer via LGMN and conferred poor prognosis. |
format | Online Article Text |
id | pubmed-8711721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87117212021-12-28 ELK1 Enhances Pancreatic Cancer Progression Via LGMN and Correlates with Poor Prognosis Yan, Qiang Ni, Chenming Lin, Yingying Sun, Xu Shen, Zhenhua Zhang, Minjie Han, Shuwen Shi, Jiemin Mao, Jing Yang, Zhe Wang, Weilin Front Mol Biosci Molecular Biosciences Pancreatic cancer is one of the most lethal cancers and its prognosis is extremely poor. Clarification of molecular mechanisms and identification of prognostic biomarkers are urgently needed. Though we previously found that LGMN was involved in pancreatic carcinoma progression, the upstream regulation of LGMN remains unknown. We used reliable software to search for the potential transcription factors that may be related with LGMN transcription, we found that ELK1 could be a new regulator of LGMN transcription that binded directly to the LGMN promoter. Moreover, knocking down of ELK1 reduced pancreatic cancer cells proliferation, invasion and survival, while LGMN restored the malignancy of pancreatic cancer in vitro and in vivo. Overexpression of ELK1 further increased cancer cells proliferation, invasion and survival. Clinically, ELK1 and LGMN were positively correlated with clinical stage, degree of differentiation and Lymph node infiltration. ELK1 and LGMN were identified as independent prognostic factors for overall survival. The patients with low expression of ELK1/LGMN survived an average of 29.65 months, whereas those with high expression of ELK1/LGMN survived an average of 16.67 months. In conclusive, our results revealed a new mechanism by which ELK1 promoted the progression of pancreatic cancer via LGMN and conferred poor prognosis. Frontiers Media S.A. 2021-12-13 /pmc/articles/PMC8711721/ /pubmed/34966781 http://dx.doi.org/10.3389/fmolb.2021.764900 Text en Copyright © 2021 Yan, Ni, Lin, Sun, Shen, Zhang, Han, Shi, Mao, Yang and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Yan, Qiang Ni, Chenming Lin, Yingying Sun, Xu Shen, Zhenhua Zhang, Minjie Han, Shuwen Shi, Jiemin Mao, Jing Yang, Zhe Wang, Weilin ELK1 Enhances Pancreatic Cancer Progression Via LGMN and Correlates with Poor Prognosis |
title | ELK1 Enhances Pancreatic Cancer Progression Via LGMN and Correlates with Poor Prognosis |
title_full | ELK1 Enhances Pancreatic Cancer Progression Via LGMN and Correlates with Poor Prognosis |
title_fullStr | ELK1 Enhances Pancreatic Cancer Progression Via LGMN and Correlates with Poor Prognosis |
title_full_unstemmed | ELK1 Enhances Pancreatic Cancer Progression Via LGMN and Correlates with Poor Prognosis |
title_short | ELK1 Enhances Pancreatic Cancer Progression Via LGMN and Correlates with Poor Prognosis |
title_sort | elk1 enhances pancreatic cancer progression via lgmn and correlates with poor prognosis |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711721/ https://www.ncbi.nlm.nih.gov/pubmed/34966781 http://dx.doi.org/10.3389/fmolb.2021.764900 |
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