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Describing a Transcription Factor Dependent Regulation of the MicroRNA Transcriptome
Published on: June 15, 2016
Protein inhibitor of activated STAT3 expression in lung cancer
Amy Kluge1, Snehal Dabir, Ilse Vlassenbroeck
1Division of Hematology/Oncology, Case Western Reserve University, University Hospitals Case Medical Center, Cleveland, Ohio, United States.
Abstract:
Protein Inhibitor of Activated Signal Transducer and Activators of Transcription 3 (PIAS3) is an endogenous inhibitor of STAT3 transcriptional activity. We have previously demonstrated the concentration-dependent negative regulatory effect of PIAS3 on STAT3 signaling and its capacity to decrease lung cancer proliferation and synergize with epidermal growth factor inhibition. We now investigate PIAS3 expression in both non-small cell lung cancer (NSCLC) cell lines and human resected NSCLC specimens. We also investigated the mechanism by which some lung cancers have significantly decreased PIAS3 expression. Expression of PIAS3 is variable in lung cancer cells lines with 2 of 3 squamous cell carcinoma (SCC) cell lines having no or little PIAS3 protein expression. Similarly, the majority of human SCCs of the lung lack PIAS3 expression by immunohistochemistry; this despite the finding that SCCs have significantly higher levels of PIAS3 mRNA compared to adenocarcinomas. High PIAS3 expression generally correlates with decreased phosphorylated STAT3 in both SCC cell lines and human specimens compatible with the negative regulatory effect of this protein on STAT3 signaling. To investigate this variable expression of PIAS3 we first performed sequencing of the PIAS3 gene that demonstrated single nucleotide polymorphisms but no mutations. Exposure of lung cancer cells to 5-azacytidine and trichostatin A results in a significant increase in PIAS3 mRNA and protein expression. However, methylation-specific PCR demonstrates a lack of CpG island methylation in the promoter region of PIAS3. Exposure of cells to an agent blocking proteosomal degradation results in a significant increase in PIAS3. Our data thus shows that SCC of the lung commonly lacks PIAS3 protein expression and that post-translational modifications may explain this finding in some cases. PIAS3 is a potential therapeutic molecule to target STAT3 pathway in lung cancer.
Insights
Protein Inhibitor of Activated Signal Transducer and Activators of Transcription 3 (PIAS3) is often lost in lung squamous cell carcinoma. This loss may be due to post-translational modifications, suggesting PIAS3 as a potential therapeutic target for lung cancer.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Genetics
Background:
- Protein Inhibitor of Activated Signal Transducer and Activators of Transcription 3 (PIAS3) negatively regulates STAT3 signaling.
- PIAS3 inhibits lung cancer cell proliferation and synergizes with epidermal growth factor inhibition.
- STAT3 signaling is implicated in various cancers, including non-small cell lung cancer (NSCLC).
Purpose of the Study:
- To investigate PIAS3 expression in NSCLC cell lines and patient specimens.
- To explore the mechanisms underlying decreased PIAS3 expression in lung cancer.
- To evaluate the therapeutic potential of targeting PIAS3 in lung cancer.
Main Methods:
- Immunohistochemistry and Western blotting to assess PIAS3 protein expression.
- Quantitative PCR to measure PIAS3 mRNA levels.
- Gene sequencing, methylation-specific PCR, and proteasome inhibition assays to investigate regulatory mechanisms.
Main Results:
- PIAS3 protein expression is significantly decreased or absent in most lung squamous cell carcinoma (SCC) cell lines and patient samples.
- SCCs exhibit higher PIAS3 mRNA levels compared to adenocarcinomas, suggesting post-transcriptional regulation.
- Increased PIAS3 expression observed upon treatment with 5-azacytidine, trichostatin A, or proteasome inhibitors, indicating epigenetic and post-translational regulation.
- High PIAS3 expression correlates with reduced phosphorylated STAT3 levels.
Conclusions:
- Lung SCC commonly lacks PIAS3 protein expression, despite elevated mRNA levels.
- Post-translational modifications, potentially including proteasomal degradation, contribute to reduced PIAS3 protein levels in lung SCC.
- PIAS3 represents a promising therapeutic target for modulating STAT3 signaling in lung cancer.
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