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STAT3 expression in salivary gland tumours
Vera Cavalcanti de Araújo1, Cristiane Furuse, Patricia Ramos Cury
1Department of Oral Pathology, São Leopoldo Mandic Dental Research Center, Rua José Rocha Junqueira 13, Campinas-SP 13045-755, Brazil. vcaraujo@slmandic.com.br <vcaraujo@slmandic.com.br>
Oral Oncology
|September 11, 2007
Summary
Signal transducer and activator of transcription (STAT3) nuclear expression was observed in malignant salivary gland tumors, unlike normal glands. This suggests STAT3 may play a role in tumor growth and survival.
Area of Science:
- Oncology
- Molecular Biology
- Pathology
Background:
- Signal transducer and activator of transcription 3 (STAT3) is often constitutively active in various malignant tumors.
- Understanding STAT3 expression in salivary gland tumors is crucial for identifying oncogenic pathways.
Purpose of the Study:
- To investigate the expression patterns of STAT3 and its phosphorylated form (STAT3P) in different types of salivary gland tumors.
- To determine if STAT3 nuclear localization is associated with malignancy in salivary gland neoplasms.
Main Methods:
- Immunohistochemical labeling of 50 salivary gland tumor biopsies and 10 normal salivary glands for STAT3 and STAT3P.
- Qualitative and quantitative evaluation of STAT3 and STAT3P expression in tissue sections.
Main Results:
- In normal salivary glands and pleomorphic adenomas, STAT3 was cytoplasmic and STAT3P nuclear, with exceptions in specific cell types.
- Malignant salivary gland tumors showed varied STAT3 and STAT3P expression, notably increased nuclear STAT3.
- Nuclear STAT3 was most prominent in cribriform-type adenoid cystic carcinomas; STAT3P expression varied, with some loss observed.
Conclusions:
- Nuclear localization of STAT3 in malignant salivary gland tumors may be an important oncogenic event.
- STAT3 nuclear expression might contribute to tumor cell proliferation and inhibit apoptosis in these cancers.
- Further research is needed to confirm the role of nuclear STAT3 in salivary gland tumorigenesis.