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Expression, prognosis and functional role of Thsd7a in esophageal squamous cell carcinoma of Kazakh patients, Xinjiang

Thsd7a (Thrombospondin type 1 domain containing 7a) is a critical transmembrane protein. Studies have indicated that Thsd7a was associated with cytoskeletal organization, cell migration and filopodia formation. However, the involvement of Thsd7a remains elusive in human Esophageal Squamous Cell Carc...

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Autores principales: Hou, Zhichao, Abudureheman, Abulajiang, Wang, Lei, Hasim, Ayshamgul, Ainiwaer, Julaiti, Zhang, Haiping, Niyaz, Madiniyat, Upur, Halmurat, Sheyhidin, Ilyar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601160/
https://www.ncbi.nlm.nih.gov/pubmed/28947992
http://dx.doi.org/10.18632/oncotarget.16966
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author Hou, Zhichao
Abudureheman, Abulajiang
Wang, Lei
Hasim, Ayshamgul
Ainiwaer, Julaiti
Zhang, Haiping
Niyaz, Madiniyat
Upur, Halmurat
Sheyhidin, Ilyar
author_facet Hou, Zhichao
Abudureheman, Abulajiang
Wang, Lei
Hasim, Ayshamgul
Ainiwaer, Julaiti
Zhang, Haiping
Niyaz, Madiniyat
Upur, Halmurat
Sheyhidin, Ilyar
author_sort Hou, Zhichao
collection PubMed
description Thsd7a (Thrombospondin type 1 domain containing 7a) is a critical transmembrane protein. Studies have indicated that Thsd7a was associated with cytoskeletal organization, cell migration and filopodia formation. However, the involvement of Thsd7a remains elusive in human Esophageal Squamous Cell Carcinoma (ESCC). Consequently, immunohistochemistry and reverse transcription-polymerase chain reaction were utilized to study the correlation between the expression of Thsd7a and clinical-pathological characteristics. The influence of Thsd7a on apoptosis, cell proliferating activity, cell cycle, migratory and invasive capacity was determined in Eca 109 and EC 9706 cell lines in vitro. And the influence on proliferating activity was testified using naked mice model in vivo. In addition, the potential molecular mechanism was tested by microarray. It was discovered that there is a certain correlation between Thsd7a and the Kazakh ESCC. By knocking out Thsd7a, the invasion, migration and proliferation could be decreased. And it could also arrest the cell cycle at G1 phase and increase the apoptosis rate. It was further verified that Thsd7a had obvious effect on proliferation in naked mice with xenograft of Eca109 cells. Finally, it was uncovered by microarray analysis that a variety of tumor genes and pathways related to Thsd7a. Together, it was demonstrated that Thsd7a might have a certain degree of carcinogenesis in ESCC.
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spelling pubmed-56011602017-09-25 Expression, prognosis and functional role of Thsd7a in esophageal squamous cell carcinoma of Kazakh patients, Xinjiang Hou, Zhichao Abudureheman, Abulajiang Wang, Lei Hasim, Ayshamgul Ainiwaer, Julaiti Zhang, Haiping Niyaz, Madiniyat Upur, Halmurat Sheyhidin, Ilyar Oncotarget Clinical Research Paper Thsd7a (Thrombospondin type 1 domain containing 7a) is a critical transmembrane protein. Studies have indicated that Thsd7a was associated with cytoskeletal organization, cell migration and filopodia formation. However, the involvement of Thsd7a remains elusive in human Esophageal Squamous Cell Carcinoma (ESCC). Consequently, immunohistochemistry and reverse transcription-polymerase chain reaction were utilized to study the correlation between the expression of Thsd7a and clinical-pathological characteristics. The influence of Thsd7a on apoptosis, cell proliferating activity, cell cycle, migratory and invasive capacity was determined in Eca 109 and EC 9706 cell lines in vitro. And the influence on proliferating activity was testified using naked mice model in vivo. In addition, the potential molecular mechanism was tested by microarray. It was discovered that there is a certain correlation between Thsd7a and the Kazakh ESCC. By knocking out Thsd7a, the invasion, migration and proliferation could be decreased. And it could also arrest the cell cycle at G1 phase and increase the apoptosis rate. It was further verified that Thsd7a had obvious effect on proliferation in naked mice with xenograft of Eca109 cells. Finally, it was uncovered by microarray analysis that a variety of tumor genes and pathways related to Thsd7a. Together, it was demonstrated that Thsd7a might have a certain degree of carcinogenesis in ESCC. Impact Journals LLC 2017-04-08 /pmc/articles/PMC5601160/ /pubmed/28947992 http://dx.doi.org/10.18632/oncotarget.16966 Text en Copyright: © 2017 Hou et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Clinical Research Paper
Hou, Zhichao
Abudureheman, Abulajiang
Wang, Lei
Hasim, Ayshamgul
Ainiwaer, Julaiti
Zhang, Haiping
Niyaz, Madiniyat
Upur, Halmurat
Sheyhidin, Ilyar
Expression, prognosis and functional role of Thsd7a in esophageal squamous cell carcinoma of Kazakh patients, Xinjiang
title Expression, prognosis and functional role of Thsd7a in esophageal squamous cell carcinoma of Kazakh patients, Xinjiang
title_full Expression, prognosis and functional role of Thsd7a in esophageal squamous cell carcinoma of Kazakh patients, Xinjiang
title_fullStr Expression, prognosis and functional role of Thsd7a in esophageal squamous cell carcinoma of Kazakh patients, Xinjiang
title_full_unstemmed Expression, prognosis and functional role of Thsd7a in esophageal squamous cell carcinoma of Kazakh patients, Xinjiang
title_short Expression, prognosis and functional role of Thsd7a in esophageal squamous cell carcinoma of Kazakh patients, Xinjiang
title_sort expression, prognosis and functional role of thsd7a in esophageal squamous cell carcinoma of kazakh patients, xinjiang
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601160/
https://www.ncbi.nlm.nih.gov/pubmed/28947992
http://dx.doi.org/10.18632/oncotarget.16966
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