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Expression Profile of GINS Complex Predicts the Prognosis of Pancreatic Cancer Patients

BACKGROUND: The GINS complex has been implicated in the prognosis of various cancers. It comprises four subunits, encoded by GINS1, GINS2, GINS3, and GINS4 genes. Based on the current understanding, no report exists on the role of the GINS complex in pancreatic cancer. METHODS: We employed various b...

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Autores principales: Bu, Fanqin, Zhu, Xiaojian, Yi, Xuan, Luo, Chen, Lin, Kang, Zhu, Jinfeng, Hu, Cegui, Liu, Zitao, Zhao, Jiefeng, Huang, Chao, Zhang, Wenjun, Huang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654543/
https://www.ncbi.nlm.nih.gov/pubmed/33192076
http://dx.doi.org/10.2147/OTT.S275649
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author Bu, Fanqin
Zhu, Xiaojian
Yi, Xuan
Luo, Chen
Lin, Kang
Zhu, Jinfeng
Hu, Cegui
Liu, Zitao
Zhao, Jiefeng
Huang, Chao
Zhang, Wenjun
Huang, Jun
author_facet Bu, Fanqin
Zhu, Xiaojian
Yi, Xuan
Luo, Chen
Lin, Kang
Zhu, Jinfeng
Hu, Cegui
Liu, Zitao
Zhao, Jiefeng
Huang, Chao
Zhang, Wenjun
Huang, Jun
author_sort Bu, Fanqin
collection PubMed
description BACKGROUND: The GINS complex has been implicated in the prognosis of various cancers. It comprises four subunits, encoded by GINS1, GINS2, GINS3, and GINS4 genes. Based on the current understanding, no report exists on the role of the GINS complex in pancreatic cancer. METHODS: We employed various bioinformatics databases including GEPIA, UALCAN, GEPIA2, and Kaplan Meier Plotter to identify the expression profile of the four genes (GINS1, GINS2, GINS3, and GINS4), their correlation with pancreatic cancer grade as well as their prognostic value of in pancreatic cancer. Western blotting and qRT-PCR analyses were conducted to verify the expression profiles of the four genes in pancreatic cancer. CCK8 and EdU cell experiments were conducted to reveal the role played by the four genes in pancreatic cancer cell proliferation. RESULTS: Based on GEPIA, Western blotting, and qRT-PCR analyses, all the four genes in the GINS complex were overexpressed in pancreatic cancer. Notably, the expression of each member was significantly associated with pancreatic cancer grade. The prognostic analysis revealed that not only the whole GINS complex but also each individual were prognostic biomarkers for pancreatic cancer. CCK8 and EdU experiments demonstrated that inhibition of the expression of each GINS member lowered pancreatic cancer cell proliferation. CONCLUSION: This work implicated GINS1, GINS2, GINS3, and GINS4 genes as critical prognostic markers for pancreatic cancer.
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spelling pubmed-76545432020-11-12 Expression Profile of GINS Complex Predicts the Prognosis of Pancreatic Cancer Patients Bu, Fanqin Zhu, Xiaojian Yi, Xuan Luo, Chen Lin, Kang Zhu, Jinfeng Hu, Cegui Liu, Zitao Zhao, Jiefeng Huang, Chao Zhang, Wenjun Huang, Jun Onco Targets Ther Original Research BACKGROUND: The GINS complex has been implicated in the prognosis of various cancers. It comprises four subunits, encoded by GINS1, GINS2, GINS3, and GINS4 genes. Based on the current understanding, no report exists on the role of the GINS complex in pancreatic cancer. METHODS: We employed various bioinformatics databases including GEPIA, UALCAN, GEPIA2, and Kaplan Meier Plotter to identify the expression profile of the four genes (GINS1, GINS2, GINS3, and GINS4), their correlation with pancreatic cancer grade as well as their prognostic value of in pancreatic cancer. Western blotting and qRT-PCR analyses were conducted to verify the expression profiles of the four genes in pancreatic cancer. CCK8 and EdU cell experiments were conducted to reveal the role played by the four genes in pancreatic cancer cell proliferation. RESULTS: Based on GEPIA, Western blotting, and qRT-PCR analyses, all the four genes in the GINS complex were overexpressed in pancreatic cancer. Notably, the expression of each member was significantly associated with pancreatic cancer grade. The prognostic analysis revealed that not only the whole GINS complex but also each individual were prognostic biomarkers for pancreatic cancer. CCK8 and EdU experiments demonstrated that inhibition of the expression of each GINS member lowered pancreatic cancer cell proliferation. CONCLUSION: This work implicated GINS1, GINS2, GINS3, and GINS4 genes as critical prognostic markers for pancreatic cancer. Dove 2020-11-06 /pmc/articles/PMC7654543/ /pubmed/33192076 http://dx.doi.org/10.2147/OTT.S275649 Text en © 2020 Bu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Bu, Fanqin
Zhu, Xiaojian
Yi, Xuan
Luo, Chen
Lin, Kang
Zhu, Jinfeng
Hu, Cegui
Liu, Zitao
Zhao, Jiefeng
Huang, Chao
Zhang, Wenjun
Huang, Jun
Expression Profile of GINS Complex Predicts the Prognosis of Pancreatic Cancer Patients
title Expression Profile of GINS Complex Predicts the Prognosis of Pancreatic Cancer Patients
title_full Expression Profile of GINS Complex Predicts the Prognosis of Pancreatic Cancer Patients
title_fullStr Expression Profile of GINS Complex Predicts the Prognosis of Pancreatic Cancer Patients
title_full_unstemmed Expression Profile of GINS Complex Predicts the Prognosis of Pancreatic Cancer Patients
title_short Expression Profile of GINS Complex Predicts the Prognosis of Pancreatic Cancer Patients
title_sort expression profile of gins complex predicts the prognosis of pancreatic cancer patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7654543/
https://www.ncbi.nlm.nih.gov/pubmed/33192076
http://dx.doi.org/10.2147/OTT.S275649
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