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Down-Regulated Microrna 148B Expression As Predictive Biomarker and Its Prognostic Significance Associated With Clinicopathological Features in Non-Small-Cell Lung Cancer Patients Publisher Pubmed



Ghasemkhani N1 ; Shadvar S1 ; Masoudi Y2 ; Talaei AJ3 ; Yahaghi E4 ; Goudarzi PK5 ; Shakiba E6
Authors
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Authors Affiliations
  1. 1. Tehran University of Medical Science, Brain and Spinal Injury Research Center, Neuroscience institute, Tehran, Iran
  2. 2. Azad University of Varamin Pishva Branch, Department of Biophysics, Faculty of Life Science, Varamin, Iran
  3. 3. Azad University of Tehran Medical Sciences Branch, Department of Genetics, Faculty of Life Science, Tehran, Iran
  4. 4. Baqiyatallah University of Medical Sciences, Department of Molecular Biology, Tehran, Iran
  5. 5. AJA University of Medical Sciences, Department of Neurosurgery, Tehran, Iran
  6. 6. Medical School, Kermanshah University of Medical Sciences, Department of Biochemistry, Kermanshah, Iran

Source: Diagnostic Pathology Published:2015


Abstract

Background: Lung cancer is most common and is the leading cause of cancer-related death in both men and women worldwide. Understanding of the molecular mechanisms underlying non-small cell lung cancer (NSCLC) development and progression are important. In the present study, we investigated the potential role of miR-148b expression analysis as potential lung cancer biomarker with the correlation of circulating miR-148b to clinicopathological features. Methods: A total of 104 NSCLC patients were diagnosed and cancer tissues together with adjacent normal tissues were evaluated. Quantitative Real-time PCR method was utilized to evaluate the expression levels of miR-148b. In addition, we investigated to clarify the relationship of miR-148b with clinicopathological features and survival in patients with NSCLC. Results: Our findings showed that miR-148b was downregulated in tumor tissues when compared with corresponding adjacent normal lung tissues (0.34 ± 0.13 vs. 1.00 ± 0.57, P < 0.05). Moreover decreased expression of miR-148b was significantly related to TNM stage (P = 0.001) and lymph node-metastasis (P = 0.023). This findings suggested that miR-148b was down-regulated in NSCLC patients and may play a key role as a tumor suppressor gene in NSCLC. Kaplan-Meier survival analysis and log-rank test suggested that low-expression group of patients had significantly shorter overall survival than high-expression group (log-rank test: P = 0.031). Multivariate Cox proportional hazards model analysis indicated that low miR-148b expression was independently linked to poor survival of patients with NSCLC (HR = 3.215, 95 % CI: 1.543-10.621, P = 0.021) and other factors were not significant independent predictor of survival in patients with NSCLC. Conclusion: Our findings demonstrated that miR-148b may play a role as independent prognostic factor for patients with NSCLC. © 2015 Ghasemkhani et al.
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