Literature DB >> 30598339

Is co-expression of USP22 and HSP90 more effective in predicting prognosis of gastric cancer?

Hongqun Zheng1, Jinling Yu2, Weihua Li3, Dongdong Yang1, Changlu Gao1, Qifan Zhang4, Lishan Xu5.   

Abstract

The ubiquitin-specific peptidase 22 (USP22) belongs to the largest subfamily of deubiquitylases and recent studies indicate that overexpression of USP22 may promote gastric cancer progression and predict prognosis. But little is known about the interaction network of USP22 in gastric cancer. In this study, we applied bioinformatics methods and found that USP22 was correlated with the heat shock protein 90 (HSP90) which is now considered to be a biomarker to predict the prognosis of gastric cancer. Then the siRNA transfection and western blotting were used to testify the correlation of USP22 and HSP90 in gastric cancer cells. The immunohistochemistry staining of the microarrays was applied to confirm the correlation of USP22 and HSP90 expression in gastric cancer tissue and further analysis showed that co-expression of USP22 and HSP90 was related to lymph node metastasis and more effective in predicting the prognosis of gastric cancer. In summary, our data demonstrate that correlation exists between USP22 and HSP90 expressions in gastric cancer and co-expression of USP22 and HSP90 may be more effective in predicting prognosis of gastric cancer.
Copyright © 2018 Elsevier GmbH. All rights reserved.

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Keywords:  Gastric cancer; Heat shock protein 90; Metastasis; Prognosis; Ubiquitin-specific peptidase 22

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Year:  2018        PMID: 30598339     DOI: 10.1016/j.prp.2018.12.020

Source DB:  PubMed          Journal:  Pathol Res Pract        ISSN: 0344-0338            Impact factor:   3.250


  1 in total

Review 1.  Clinicopathological and Prognostic Value of USP22 Expression in Gastric Cancer: A Systematic Review and Meta-Analysis and Database Validation.

Authors:  Yuhang Wang; Zirui Jia; Jiacheng Gao; Tingting Zhou; Xiangwen Zhang; Guo Zu
Journal:  Front Surg       Date:  2022-06-16
  1 in total

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