Cargando…
Identification of candidate genes or microRNAs associated with the lymph node metastasis of SCLC
BACKGROUND: Small cell lung cancer (SCLC) is a highly malignant cancer, and over 70% of patients with SCLC present with the metastatic disease. We aimed to explore some novel differentially expressed genes (DEGs) or microRNAs (miRNAs) associated with the lymph node metastasis of SCLC. METHODS: The D...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194557/ https://www.ncbi.nlm.nih.gov/pubmed/30364292 http://dx.doi.org/10.1186/s12935-018-0653-5 |
_version_ | 1783364246888775680 |
---|---|
author | Wang, Zhonghao Lu, Bei Sun, Lixin Yan, Xi Xu, Jinzhi |
author_facet | Wang, Zhonghao Lu, Bei Sun, Lixin Yan, Xi Xu, Jinzhi |
author_sort | Wang, Zhonghao |
collection | PubMed |
description | BACKGROUND: Small cell lung cancer (SCLC) is a highly malignant cancer, and over 70% of patients with SCLC present with the metastatic disease. We aimed to explore some novel differentially expressed genes (DEGs) or microRNAs (miRNAs) associated with the lymph node metastasis of SCLC. METHODS: The DEGs between the metastasis and cancer groups were identified, and GO functional and KEGG pathway enrichment analyses for these DEGs were implemented. Subsequently, the protein–protein interaction network and subnetwork of module were constructed. Then the regulatory networks based on miRNAs, transcription factors (TFs) and target DEGs were constructed. Ultimately, the survival analysis for DEGs was performed to obtain the DEGs related to the survival of SCLC. RESULTS: Here, 186 upregulated (e.g., GSR, HCP5) and 144 downregulated DEGs (e.g., MET, GRM8, and DACH1) were identified between the SCLC patients with lymph node metastasis and without lymph node metastasis. GRM8 was attracted to the G-protein coupled receptor signaling pathway. Besides, miR-126 was identified in the miRNAs-TFs-target regulatory network. GRM8 and DACH1 were all regulated by miR-126. In particular, GSR and HCP5 were correlated with survival of SCLC patients. CONCLUSION: MiR-126, DACH1, GRM8, MET, GSR, and HCP5 were implicated in the lymph node metastasis process of SCLC. |
format | Online Article Text |
id | pubmed-6194557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61945572018-10-25 Identification of candidate genes or microRNAs associated with the lymph node metastasis of SCLC Wang, Zhonghao Lu, Bei Sun, Lixin Yan, Xi Xu, Jinzhi Cancer Cell Int Primary Research BACKGROUND: Small cell lung cancer (SCLC) is a highly malignant cancer, and over 70% of patients with SCLC present with the metastatic disease. We aimed to explore some novel differentially expressed genes (DEGs) or microRNAs (miRNAs) associated with the lymph node metastasis of SCLC. METHODS: The DEGs between the metastasis and cancer groups were identified, and GO functional and KEGG pathway enrichment analyses for these DEGs were implemented. Subsequently, the protein–protein interaction network and subnetwork of module were constructed. Then the regulatory networks based on miRNAs, transcription factors (TFs) and target DEGs were constructed. Ultimately, the survival analysis for DEGs was performed to obtain the DEGs related to the survival of SCLC. RESULTS: Here, 186 upregulated (e.g., GSR, HCP5) and 144 downregulated DEGs (e.g., MET, GRM8, and DACH1) were identified between the SCLC patients with lymph node metastasis and without lymph node metastasis. GRM8 was attracted to the G-protein coupled receptor signaling pathway. Besides, miR-126 was identified in the miRNAs-TFs-target regulatory network. GRM8 and DACH1 were all regulated by miR-126. In particular, GSR and HCP5 were correlated with survival of SCLC patients. CONCLUSION: MiR-126, DACH1, GRM8, MET, GSR, and HCP5 were implicated in the lymph node metastasis process of SCLC. BioMed Central 2018-10-19 /pmc/articles/PMC6194557/ /pubmed/30364292 http://dx.doi.org/10.1186/s12935-018-0653-5 Text en © The Author(s) 2018 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, Zhonghao Lu, Bei Sun, Lixin Yan, Xi Xu, Jinzhi Identification of candidate genes or microRNAs associated with the lymph node metastasis of SCLC |
title | Identification of candidate genes or microRNAs associated with the lymph node metastasis of SCLC |
title_full | Identification of candidate genes or microRNAs associated with the lymph node metastasis of SCLC |
title_fullStr | Identification of candidate genes or microRNAs associated with the lymph node metastasis of SCLC |
title_full_unstemmed | Identification of candidate genes or microRNAs associated with the lymph node metastasis of SCLC |
title_short | Identification of candidate genes or microRNAs associated with the lymph node metastasis of SCLC |
title_sort | identification of candidate genes or micrornas associated with the lymph node metastasis of sclc |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194557/ https://www.ncbi.nlm.nih.gov/pubmed/30364292 http://dx.doi.org/10.1186/s12935-018-0653-5 |
work_keys_str_mv | AT wangzhonghao identificationofcandidategenesormicrornasassociatedwiththelymphnodemetastasisofsclc AT lubei identificationofcandidategenesormicrornasassociatedwiththelymphnodemetastasisofsclc AT sunlixin identificationofcandidategenesormicrornasassociatedwiththelymphnodemetastasisofsclc AT yanxi identificationofcandidategenesormicrornasassociatedwiththelymphnodemetastasisofsclc AT xujinzhi identificationofcandidategenesormicrornasassociatedwiththelymphnodemetastasisofsclc |