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Primary small cell carcinoma of the esophagus: clinicopathological study of 44 cases
BACKGROUND: Primary small cell carcinoma of the esophagus (SCCE) is a highly aggressive disease characterized by early dissemination and poor prognosis. Because of the rarity of this disease, few previous studies have investigated the biomarkers associated with its prognosis. Leucine-rich repeat-con...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987173/ https://www.ncbi.nlm.nih.gov/pubmed/24666414 http://dx.doi.org/10.1186/1471-2407-14-222 |
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author | Chen, Wei-Wei Wang, Feng Zhang, Dong-Sheng Luo, Hui-Yan Wang, Zhi-Qiang Wang, Feng-Hua Qiu, Miao-Zhen Ren, Chao Wei, Xiao-Li Wu, Wen-Jing Li, Yu-Hong Xu, Rui-Hua |
author_facet | Chen, Wei-Wei Wang, Feng Zhang, Dong-Sheng Luo, Hui-Yan Wang, Zhi-Qiang Wang, Feng-Hua Qiu, Miao-Zhen Ren, Chao Wei, Xiao-Li Wu, Wen-Jing Li, Yu-Hong Xu, Rui-Hua |
author_sort | Chen, Wei-Wei |
collection | PubMed |
description | BACKGROUND: Primary small cell carcinoma of the esophagus (SCCE) is a highly aggressive disease characterized by early dissemination and poor prognosis. Because of the rarity of this disease, few previous studies have investigated the biomarkers associated with its prognosis. Leucine-rich repeat-containing G-protein coupled receptor 5 (Lgr5) is a stem cell marker and a member of the canonical Wnt-signaling cascade. However, the clinical role of Lgr5 in SCCE remains unknown. METHODS: Tissue sections were obtained from 44 patients diagnosed with SCCE and expression of Lgr5 was examined by immunohistochemistry. The correlations between Lgr5 expression, and clinical parameters and prognostic significance were evaluated. RESULTS: Lgr5 was expressed in SCCE cancer tissues. High Lgr5 expression was significantly correlated with lymph node metastasis (p = 0.003), late stage (p = 0.003) and unfavorable response to chemotherapy (p = 0.013) according to RECIST 1.0 criteria. Patients with higher Lgr5 expression levels had shorter overall survival times than those with lower expression levels. CONCLUSIONS: These results demonstrated that overexpression of Lgr5 was significantly correlated with lymph node metastasis, tumor stage, and response to chemotherapy. Furthermore, high levels of Lgr5 expression appeared to be associated with poorer survival in patients with SCCE. |
format | Online Article Text |
id | pubmed-3987173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39871732014-04-16 Primary small cell carcinoma of the esophagus: clinicopathological study of 44 cases Chen, Wei-Wei Wang, Feng Zhang, Dong-Sheng Luo, Hui-Yan Wang, Zhi-Qiang Wang, Feng-Hua Qiu, Miao-Zhen Ren, Chao Wei, Xiao-Li Wu, Wen-Jing Li, Yu-Hong Xu, Rui-Hua BMC Cancer Research Article BACKGROUND: Primary small cell carcinoma of the esophagus (SCCE) is a highly aggressive disease characterized by early dissemination and poor prognosis. Because of the rarity of this disease, few previous studies have investigated the biomarkers associated with its prognosis. Leucine-rich repeat-containing G-protein coupled receptor 5 (Lgr5) is a stem cell marker and a member of the canonical Wnt-signaling cascade. However, the clinical role of Lgr5 in SCCE remains unknown. METHODS: Tissue sections were obtained from 44 patients diagnosed with SCCE and expression of Lgr5 was examined by immunohistochemistry. The correlations between Lgr5 expression, and clinical parameters and prognostic significance were evaluated. RESULTS: Lgr5 was expressed in SCCE cancer tissues. High Lgr5 expression was significantly correlated with lymph node metastasis (p = 0.003), late stage (p = 0.003) and unfavorable response to chemotherapy (p = 0.013) according to RECIST 1.0 criteria. Patients with higher Lgr5 expression levels had shorter overall survival times than those with lower expression levels. CONCLUSIONS: These results demonstrated that overexpression of Lgr5 was significantly correlated with lymph node metastasis, tumor stage, and response to chemotherapy. Furthermore, high levels of Lgr5 expression appeared to be associated with poorer survival in patients with SCCE. BioMed Central 2014-03-25 /pmc/articles/PMC3987173/ /pubmed/24666414 http://dx.doi.org/10.1186/1471-2407-14-222 Text en Copyright © 2014 Chen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 | Research Article Chen, Wei-Wei Wang, Feng Zhang, Dong-Sheng Luo, Hui-Yan Wang, Zhi-Qiang Wang, Feng-Hua Qiu, Miao-Zhen Ren, Chao Wei, Xiao-Li Wu, Wen-Jing Li, Yu-Hong Xu, Rui-Hua Primary small cell carcinoma of the esophagus: clinicopathological study of 44 cases |
title | Primary small cell carcinoma of the esophagus: clinicopathological study of 44 cases |
title_full | Primary small cell carcinoma of the esophagus: clinicopathological study of 44 cases |
title_fullStr | Primary small cell carcinoma of the esophagus: clinicopathological study of 44 cases |
title_full_unstemmed | Primary small cell carcinoma of the esophagus: clinicopathological study of 44 cases |
title_short | Primary small cell carcinoma of the esophagus: clinicopathological study of 44 cases |
title_sort | primary small cell carcinoma of the esophagus: clinicopathological study of 44 cases |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987173/ https://www.ncbi.nlm.nih.gov/pubmed/24666414 http://dx.doi.org/10.1186/1471-2407-14-222 |
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