Increased Expression of p-GSK3β Predicts Poor Survival in T -III/IV Stage OSCC Patients.


Journal

In vivo (Athens, Greece)
ISSN: 1791-7549
Titre abrégé: In Vivo
Pays: Greece
ID NLM: 8806809

Informations de publication

Date de publication:
Historique:
received: 21 03 2020
revised: 12 04 2020
accepted: 13 04 2020
entrez: 2 7 2020
pubmed: 2 7 2020
medline: 22 6 2021
Statut: ppublish

Résumé

Glycogen synthase kinase 3 beta (GSK3-β) acts either as a tumor suppressor or an oncogene in various human cancers. The present study aimed to investigate the expression and activity of p-GSK3-β (Ser9) in oral cancer patients. We investigated the levels of p-GSK3β in 152 oral cancer tissues by immunohistochemistry, and explored their prognostic impact. To investigate the role of p-GSK3β (Ser9) in OSCC progression, we first analyzed the expression levels of protein p-GSK3β in normal and oral cancer tissues using immunohistochemical staining. p-GSK3β immunostaining was detected in 32 of 152 (21.1%) oral cancer specimens. High p-GSK3β expression was significantly associated with T (III/IV) stage. Kaplan-Meier survival analysis revealed that high levels of p-GSK3β were correlated with poor survival (p=0.001) in T stage (III/IV) OSCC patients. Multivariate analyses indicated that TN stage, AJCC tumor stage, tumor differentiation status and clinical therapy, but not p-GSK3β levels, were independent prognostic factors. Significant mortality risk was found in T stage (III/IV) oral cancer patients with high levels of p-GSK3β (p=0.0006). GSK3β inactivation is a key event in oral cancer patients and targeting GSK3β might be valuable in treating oral cancer patients.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Glycogen synthase kinase 3 beta (GSK3-β) acts either as a tumor suppressor or an oncogene in various human cancers. The present study aimed to investigate the expression and activity of p-GSK3-β (Ser9) in oral cancer patients.
MATERIALS AND METHODS METHODS
We investigated the levels of p-GSK3β in 152 oral cancer tissues by immunohistochemistry, and explored their prognostic impact.
RESULTS RESULTS
To investigate the role of p-GSK3β (Ser9) in OSCC progression, we first analyzed the expression levels of protein p-GSK3β in normal and oral cancer tissues using immunohistochemical staining. p-GSK3β immunostaining was detected in 32 of 152 (21.1%) oral cancer specimens. High p-GSK3β expression was significantly associated with T (III/IV) stage. Kaplan-Meier survival analysis revealed that high levels of p-GSK3β were correlated with poor survival (p=0.001) in T stage (III/IV) OSCC patients. Multivariate analyses indicated that TN stage, AJCC tumor stage, tumor differentiation status and clinical therapy, but not p-GSK3β levels, were independent prognostic factors. Significant mortality risk was found in T stage (III/IV) oral cancer patients with high levels of p-GSK3β (p=0.0006).
CONCLUSION CONCLUSIONS
GSK3β inactivation is a key event in oral cancer patients and targeting GSK3β might be valuable in treating oral cancer patients.

Identifiants

pubmed: 32606150
pii: 34/4/1805
doi: 10.21873/invivo.11975
pmc: PMC7439907
doi:

Substances chimiques

Glycogen Synthase Kinase 3 beta EC 2.7.11.1
Glycogen Synthase Kinase 3 EC 2.7.11.26

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1805-1809

Informations de copyright

Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

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Auteurs

Bharath Kumar Velmurugan (BK)

Department of Biotechnology, Asia University, Taichung, Taiwan, R.O.C.

Chun-Wen Chiu (CW)

Department of Emergency Medicine, Changhua Christian Hospital, Changhua, Taiwan, R.O.C.

Yueh-Min Lin (YM)

Department of Surgical Pathology, Changhua Christian Hospital, Changhua, Taiwan, R.O.C.
School of Medicine, Chung Shan Medical University, Taichung, Taiwan, R.O.C.
Department of Medical Laboratory Science and Biotechnology, Central Taiwan University of Science and Technology, Taichung, Taiwan, R.O.C.

Mahalakshmi Bharath (M)

Institute of Research and Development, Duy Tan University, Da Nang, Vietnam.

Chung-Min Yeh (CM)

Department of Surgical Pathology, Changhua Christian Hospital, Changhua, Taiwan, R.O.C.
Department of Medical Technology, Jen-Teh Junior College of Medicine, Nursing and Management, Miaoli, Taiwan, R.O.C.

Yu-En Chen (YE)

Department of Surgical Pathology, Changhua Christian Hospital, Changhua, Taiwan, R.O.C.

Chia-Min Chung (CM)

Graduate Institute of BioMedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.
Environment-Omics-Diseases Research Center, China Medical University Hospital, Taichung, Taiwan, R.O.C.

Shu-Hui Lin (SH)

Department of Surgical Pathology, Changhua Christian Hospital, Changhua, Taiwan, R.O.C. 74630@cch.org.tw.
Department of Medical Laboratory Science and Biotechnology, Central Taiwan University of Science and Technology, Taichung, Taiwan, R.O.C.

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