Cargando…
A novel long non-coding RNA-KAT7 is low expressed in colorectal cancer and acts as a tumor suppressor
BACKGROUND: The abnormal expression of many long non-coding RNAs (lncRNAs) has been reported in the progression of various tumors. However, the potential biological roles and regulatory mechanisms of long non-coding RNAs in the development of colorectal cancer (CRC) have not yet been fully elucidate...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390533/ https://www.ncbi.nlm.nih.gov/pubmed/30858757 http://dx.doi.org/10.1186/s12935-019-0760-y |
_version_ | 1783398156471369728 |
---|---|
author | Wang, Qingmei He, Rongzhang Tan, Tan Li, Jia Hu, Zheng Luo, Weihao Duan, Lili Luo, Wenna Luo, Dixian |
author_facet | Wang, Qingmei He, Rongzhang Tan, Tan Li, Jia Hu, Zheng Luo, Weihao Duan, Lili Luo, Wenna Luo, Dixian |
author_sort | Wang, Qingmei |
collection | PubMed |
description | BACKGROUND: The abnormal expression of many long non-coding RNAs (lncRNAs) has been reported in the progression of various tumors. However, the potential biological roles and regulatory mechanisms of long non-coding RNAs in the development of colorectal cancer (CRC) have not yet been fully elucidated. Therefore, it is crucial to identify that lncRNAs can be used for the clinical prevention and treatment of CRC. METHODS: In our previous work, we identificated a novel lncRNA, lncRNA-KAT7, and found that the expression of lncRNA-KAT7 in CRC tissues was significantly lower than that in matched normal intestinal tissues, and the expression in CRC cell lines was lower than that of normal intestinal epithelial cells (P < 0.05). Besides, the expression of lncRNA-KAT7 is negative associated with age, tumor size, tumor differentiation, lymph node metastasis of CRC patients. The potential biological effects and molecular mechanisms of lncRNA-KAT7 in CRC were evaluated using a series of CCK-8 assay, clone formation assay, EdU proliferation assay, scratch determination, transwell determination, western blot analysis, and nude subcutaneous tumorigenesis model construction cell and animal experiments. RESULTS: The expression of lncRNA-KAT7 in CRC tissues was lower than that in matched normal tissues and normal intestinal epithelial cells (P < 0.05). Decreased expression of lncRNA-KAT7 is associated with clinicopathological features of poor CRC patients. In vitro experiments showed that up-regulation of lncRNA-KAT7 expression in CRC cells inhibited cell proliferation and migration. In vivo animal experiments showed that the lncRNA-KAT7 also inhibited tumor growth. Western blot analysis showed that the expression of lncRNA-KAT7 was up-regulated in HCT116 cells, the expression of E-cadherin increased, and the expression of Vimentin, MMP-2 and β-catenin protein was down-regulated so did the phosphorylation NF-κB P65. The results confirm that the expression of lncRAN-KAT7 can inhibit the malignant phenotype of CRC cells. CONCLUSIONS: Up to now, as a novel lncRNA, lncRNA-KAT7 has not any relevant research and reports. The results confirm that the expression of lncRNA-KAT7 can inhibit the malignant phenotype of CRC cells. And it can be used as a new diagnostic biomarker and therapeutic target for the development of CRC. |
format | Online Article Text |
id | pubmed-6390533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63905332019-03-11 A novel long non-coding RNA-KAT7 is low expressed in colorectal cancer and acts as a tumor suppressor Wang, Qingmei He, Rongzhang Tan, Tan Li, Jia Hu, Zheng Luo, Weihao Duan, Lili Luo, Wenna Luo, Dixian Cancer Cell Int Primary Research BACKGROUND: The abnormal expression of many long non-coding RNAs (lncRNAs) has been reported in the progression of various tumors. However, the potential biological roles and regulatory mechanisms of long non-coding RNAs in the development of colorectal cancer (CRC) have not yet been fully elucidated. Therefore, it is crucial to identify that lncRNAs can be used for the clinical prevention and treatment of CRC. METHODS: In our previous work, we identificated a novel lncRNA, lncRNA-KAT7, and found that the expression of lncRNA-KAT7 in CRC tissues was significantly lower than that in matched normal intestinal tissues, and the expression in CRC cell lines was lower than that of normal intestinal epithelial cells (P < 0.05). Besides, the expression of lncRNA-KAT7 is negative associated with age, tumor size, tumor differentiation, lymph node metastasis of CRC patients. The potential biological effects and molecular mechanisms of lncRNA-KAT7 in CRC were evaluated using a series of CCK-8 assay, clone formation assay, EdU proliferation assay, scratch determination, transwell determination, western blot analysis, and nude subcutaneous tumorigenesis model construction cell and animal experiments. RESULTS: The expression of lncRNA-KAT7 in CRC tissues was lower than that in matched normal tissues and normal intestinal epithelial cells (P < 0.05). Decreased expression of lncRNA-KAT7 is associated with clinicopathological features of poor CRC patients. In vitro experiments showed that up-regulation of lncRNA-KAT7 expression in CRC cells inhibited cell proliferation and migration. In vivo animal experiments showed that the lncRNA-KAT7 also inhibited tumor growth. Western blot analysis showed that the expression of lncRNA-KAT7 was up-regulated in HCT116 cells, the expression of E-cadherin increased, and the expression of Vimentin, MMP-2 and β-catenin protein was down-regulated so did the phosphorylation NF-κB P65. The results confirm that the expression of lncRAN-KAT7 can inhibit the malignant phenotype of CRC cells. CONCLUSIONS: Up to now, as a novel lncRNA, lncRNA-KAT7 has not any relevant research and reports. The results confirm that the expression of lncRNA-KAT7 can inhibit the malignant phenotype of CRC cells. And it can be used as a new diagnostic biomarker and therapeutic target for the development of CRC. BioMed Central 2019-02-26 /pmc/articles/PMC6390533/ /pubmed/30858757 http://dx.doi.org/10.1186/s12935-019-0760-y Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Primary Research Wang, Qingmei He, Rongzhang Tan, Tan Li, Jia Hu, Zheng Luo, Weihao Duan, Lili Luo, Wenna Luo, Dixian A novel long non-coding RNA-KAT7 is low expressed in colorectal cancer and acts as a tumor suppressor |
title | A novel long non-coding RNA-KAT7 is low expressed in colorectal cancer and acts as a tumor suppressor |
title_full | A novel long non-coding RNA-KAT7 is low expressed in colorectal cancer and acts as a tumor suppressor |
title_fullStr | A novel long non-coding RNA-KAT7 is low expressed in colorectal cancer and acts as a tumor suppressor |
title_full_unstemmed | A novel long non-coding RNA-KAT7 is low expressed in colorectal cancer and acts as a tumor suppressor |
title_short | A novel long non-coding RNA-KAT7 is low expressed in colorectal cancer and acts as a tumor suppressor |
title_sort | novel long non-coding rna-kat7 is low expressed in colorectal cancer and acts as a tumor suppressor |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390533/ https://www.ncbi.nlm.nih.gov/pubmed/30858757 http://dx.doi.org/10.1186/s12935-019-0760-y |
work_keys_str_mv | AT wangqingmei anovellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT herongzhang anovellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT tantan anovellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT lijia anovellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT huzheng anovellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT luoweihao anovellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT duanlili anovellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT luowenna anovellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT luodixian anovellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT wangqingmei novellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT herongzhang novellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT tantan novellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT lijia novellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT huzheng novellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT luoweihao novellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT duanlili novellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT luowenna novellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor AT luodixian novellongnoncodingrnakat7islowexpressedincolorectalcancerandactsasatumorsuppressor |