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A research of STEAP1 regulated gastric cancer cell proliferation, migration and invasion in vitro and in vivos

Six‐Transmembrane Epithelial Antigene of the Prostate 1 (STEAP1) is associated with the occurrence and development of cancer. This study aimed to clarify the role of STEAP1 in gastric cancer tumour growth and metastasis, as well as its molecular mechanism of action.Statistical methods were used for...

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Autores principales: Zhang, Zhe, Hou, Wen‐bin, Zhang, Chao, Tan, Yu‐en, Zhang, Dong‐dong, An, Wen, Pan, Si‐wei, Wu, Wan‐di, Chen, Qing‐chuan, Xu, Hui‐mian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754049/
https://www.ncbi.nlm.nih.gov/pubmed/33128353
http://dx.doi.org/10.1111/jcmm.16038
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author Zhang, Zhe
Hou, Wen‐bin
Zhang, Chao
Tan, Yu‐en
Zhang, Dong‐dong
An, Wen
Pan, Si‐wei
Wu, Wan‐di
Chen, Qing‐chuan
Xu, Hui‐mian
author_facet Zhang, Zhe
Hou, Wen‐bin
Zhang, Chao
Tan, Yu‐en
Zhang, Dong‐dong
An, Wen
Pan, Si‐wei
Wu, Wan‐di
Chen, Qing‐chuan
Xu, Hui‐mian
author_sort Zhang, Zhe
collection PubMed
description Six‐Transmembrane Epithelial Antigene of the Prostate 1 (STEAP1) is associated with the occurrence and development of cancer. This study aimed to clarify the role of STEAP1 in gastric cancer tumour growth and metastasis, as well as its molecular mechanism of action.Statistical methods were used for clinical data analysis. Protein expression was detected using immunohistochemistry(IHC). The mRNA and protein expression in the cell cultures were detected using reverse transcription‐polymerase chain reaction(RT‐PCR) and western blot analysis. Overexpression and silencing models were constructed using plasmid and lentivirus transfection. To detect cell proliferation in vitro, Cell Counting Kit‐8(CCK‐8), flow cytometry and colony formation assays were used; transwell and wound healing assays were used to detect cell migration and invasion;For in vivo experiments, nude BALB/c mice were used for detecting subcutaneous tumorigenesis and intraperitoneal implantation. In the results,we found STEAP1 was overexpressed in gastric cancer tissues and cell lines. Single‐factor and Cox analyses showed that STEAP1 gene expression level correlated with poor prognosis. Up‐regulation of STEAP1 increased cell proliferation, migration and invasion, which decreased after STEAP1 was knocked down. These changes were achieved via the activation of the AKT/FoxO1 pathway and epithelial‐mesenchymal transformation (EMT). The in vivo animal experiments showed that STEAP1 knock down, resulted in a decrease in the subcutaneous tumour and peritoneal tumour formation.
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spelling pubmed-77540492020-12-23 A research of STEAP1 regulated gastric cancer cell proliferation, migration and invasion in vitro and in vivos Zhang, Zhe Hou, Wen‐bin Zhang, Chao Tan, Yu‐en Zhang, Dong‐dong An, Wen Pan, Si‐wei Wu, Wan‐di Chen, Qing‐chuan Xu, Hui‐mian J Cell Mol Med Original Articles Six‐Transmembrane Epithelial Antigene of the Prostate 1 (STEAP1) is associated with the occurrence and development of cancer. This study aimed to clarify the role of STEAP1 in gastric cancer tumour growth and metastasis, as well as its molecular mechanism of action.Statistical methods were used for clinical data analysis. Protein expression was detected using immunohistochemistry(IHC). The mRNA and protein expression in the cell cultures were detected using reverse transcription‐polymerase chain reaction(RT‐PCR) and western blot analysis. Overexpression and silencing models were constructed using plasmid and lentivirus transfection. To detect cell proliferation in vitro, Cell Counting Kit‐8(CCK‐8), flow cytometry and colony formation assays were used; transwell and wound healing assays were used to detect cell migration and invasion;For in vivo experiments, nude BALB/c mice were used for detecting subcutaneous tumorigenesis and intraperitoneal implantation. In the results,we found STEAP1 was overexpressed in gastric cancer tissues and cell lines. Single‐factor and Cox analyses showed that STEAP1 gene expression level correlated with poor prognosis. Up‐regulation of STEAP1 increased cell proliferation, migration and invasion, which decreased after STEAP1 was knocked down. These changes were achieved via the activation of the AKT/FoxO1 pathway and epithelial‐mesenchymal transformation (EMT). The in vivo animal experiments showed that STEAP1 knock down, resulted in a decrease in the subcutaneous tumour and peritoneal tumour formation. John Wiley and Sons Inc. 2020-10-30 2020-12 /pmc/articles/PMC7754049/ /pubmed/33128353 http://dx.doi.org/10.1111/jcmm.16038 Text en © 2020 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Zhang, Zhe
Hou, Wen‐bin
Zhang, Chao
Tan, Yu‐en
Zhang, Dong‐dong
An, Wen
Pan, Si‐wei
Wu, Wan‐di
Chen, Qing‐chuan
Xu, Hui‐mian
A research of STEAP1 regulated gastric cancer cell proliferation, migration and invasion in vitro and in vivos
title A research of STEAP1 regulated gastric cancer cell proliferation, migration and invasion in vitro and in vivos
title_full A research of STEAP1 regulated gastric cancer cell proliferation, migration and invasion in vitro and in vivos
title_fullStr A research of STEAP1 regulated gastric cancer cell proliferation, migration and invasion in vitro and in vivos
title_full_unstemmed A research of STEAP1 regulated gastric cancer cell proliferation, migration and invasion in vitro and in vivos
title_short A research of STEAP1 regulated gastric cancer cell proliferation, migration and invasion in vitro and in vivos
title_sort research of steap1 regulated gastric cancer cell proliferation, migration and invasion in vitro and in vivos
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7754049/
https://www.ncbi.nlm.nih.gov/pubmed/33128353
http://dx.doi.org/10.1111/jcmm.16038
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