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Aberrant expression of glycogen synthase kinase-3β in human breast and head and neck cancer. | LitMetric

AI Article Synopsis

  • Glycogen Synthase Kinase-3β (GSK-3β) is being studied as a possible therapeutic target in human cancers, particularly breast and head and neck cancers.
  • The study found that abnormal levels of GSK-3β in the nucleus are present in a high percentage of breast cancer cases but not in benign tissue, suggesting its potential role as a biomarker.
  • Additionally, the presence of nuclear GSK-3β in various cancer types correlates with specific tumor characteristics, indicating its significance in cancer treatment strategies.

Article Abstract

Glycogen Synthase Kinase-3β (GSK-3β), a serine/threonine protein kinase, has been implicated as a potential therapeutic target in human cancer. The objective of the present study was to evaluate aberrant expression of GSK-3β as a potential biomarker in human breast and head and neck cancers. Nuclear/cytosolic fractionation, immunoblotting and immunohistochemical staining was used to study the expression of GSK-3β in human breast and head and neck cancer. Aberrant nuclear accumulation of GSK-3β in five human breast cancer cell lines was demonstrated and in 89/128 (70%) human breast carcinomas, whereas no detectable expression of GSK-3β was found in benign breast tissue. Nuclear GSK-3β expression was associated with HER-2 positive tumors (P=0.02) and non-triple negative breast carcinomas (P=0.0001), although nuclear GSK-3β was observed in some samples across all breast cancer subtypes. Aberrant nuclear expression of GSK-3β was found in 11/15 (73%) squamous cell head and neck carcinomas, whereas weak or no detectable expression of GSK-3β was found in benign salivary gland and other benign head and neck tissues. These results support the hypothesis that aberrant nuclear GSK-3β may represent a potential target for the clinical treatment of human breast and squamous cell carcinoma.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202539PMC
http://dx.doi.org/10.3892/ol.2018.9483DOI Listing

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