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miR-34a is downregulated in cis-diamminedichloroplatinum treated sinonasal squamous cell carcinoma patients with poor
Takenori Ogawa1, Yuriko Saiki, Kiyoto Shiga
1Department of Molecular Pathology, Tohoku University School of Medicine, Miyagi, Japan. ogawa@orl.med.tohoku.ac.jp
Abstract:
For the purpose of analyzing mechanisms related to the cis-diamminedichloroplatinum resistance in head and neck squamous cell carcinoma, we analyzed RPMI2650 and its derived previously established cis-diamminedichloroplatinum resistant cell line RPMI2650CR. To identify resistant phenotype-related microRNAs, we compared microRNA expressions between RPMI2650CR and RPMI2650 by microarray. One of the microRNAs as downregulated, miR-34a, was further investigated. Decreased expression of miR-34a in RPMI2650CR was confirmed by quantitative reverse transcription-polymerase chain reaction, but introduction of the miR-34a precursor into RPMI2650CR or the inhibitor of miR-34a into RPMI2650 did not change cis-diamminedichloroplatinum sensitivities. However, 24 patients with sinonasal squamous cell carcinomas treated with intra-arterial infusion of cis-diamminedichloroplatinum showed a significant association between decreased expression of miR-34a and poor disease specific survival (P = 0.0015), poor disease free survival (P = 0.0019), and poor local control rates (P = 0.017) (median follow-up period: 53 months). Furthermore, multivariate analyses demonstrated significant associations between miR-34a expression and the hazard ratios of disease free survival at 0.005 (95% confidence interval [CI] 0.00-0.29, P = 0.011) and local control rate at 0.008 (95% CI 0.00-0.44, P = 0.019), although other parameters such as age, gender, treatment method, T and N stages did not show any similar association. These results strongly suggest that miR-34a expression can be an independent prognostic biomarker in patients with sinonasal squamous cell carcinoma who are undergoing treatment with cis-diamminedichloroplatinum.
Insights
MicroRNA-34a (miR-34a) downregulation is linked to poor outcomes in sinonasal squamous cell carcinoma patients treated with cis-diamminedichloroplatinum. This suggests miR-34a is a potential prognostic biomarker for this cancer.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Cis-diamminedichloroplatinum (CDDP) is a key chemotherapy for head and neck squamous cell carcinoma.
- Mechanisms of CDDP resistance are not fully understood.
- MicroRNAs (miRNAs) play roles in cancer development and drug resistance.
Purpose of the Study:
- To investigate the role of microRNAs in CDDP resistance in head and neck squamous cell carcinoma.
- To identify potential biomarkers for predicting treatment response and prognosis.
Main Methods:
- Comparison of miRNA expression profiles between CDDP-sensitive (RPMI2650) and CDDP-resistant (RPMI2650CR) cell lines using microarray.
- Validation of miR-34a downregulation by quantitative reverse transcription-polymerase chain reaction (qRT-PCR).
- Analysis of miR-34a expression in relation to clinical outcomes in 24 sinonasal squamous cell carcinoma patients treated with CDDP.
Main Results:
- miR-34a was found to be significantly downregulated in the CDDP-resistant cell line.
- Functional studies introducing miR-34a or its inhibitor did not alter CDDP sensitivity in cell lines.
- Decreased miR-34a expression in patients correlated significantly with poor disease-specific survival, disease-free survival, and local control rates.
- Multivariate analysis confirmed miR-34a expression as an independent prognostic factor for disease-free survival and local control.
Conclusions:
- miR-34a downregulation is associated with poor prognosis in sinonasal squamous cell carcinoma patients treated with CDDP.
- miR-34a expression serves as a potential independent prognostic biomarker for predicting treatment outcomes in this patient group.
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