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Identification of a three-miRNA signature as a blood-borne diagnostic marker for early diagnosis of lung adenocarcinoma.

AbstractBACKGROUND:
The subtypes of NSCLC have unique characteristics of pathogenic mechanism and responses to targeted therapies. Thus, non-invasive markers for diagnosis of different subtypes of NSCLC at early stage are needed.
RESULTS:
Based on the results from the screening and validation process, 3 miRNAs (miR-532, miR-628-3p and miR-425-3p) were found to display significantly different expression levels in early-stage lung adenocarcinoma, as compared to those in healthy controls. ROC analysis showed that the miRNA-based biomarker could distinguish lung adenocarcinoma from healthy controls with high AUC (0.974), sensitivity (91.5%), and specificity (97.8%). Importantly, these three miRNAs could also distinguish lung adenocarcinoma from lung benigh diseases and other subtypes of lung cancer.
METHODS:
Two hundreds and one early-stage lung adenocarcinoma cases and one hundreds seventy eight age- and sex-matched healthy controls were recruited to this study. We screened the differentially expressed plasma miRNAs using TaqMan Low Density Arrays (TLDA) followed by three-phase qRT-PCR validation. A risk score model was established to evaluate the diagnostic value of the plasma miRNA profiling system.
CONCLUSIONS:
Taken together, these findings suggest that the 3 miRNA-based biomarker might serve as a novel non-invasive approach for diagnosis of early-stage lung adenocarcinoma.
AuthorsYang Wang, Hua Zhao, Xujie Gao, Feng Wei, Xinwei Zhang, Yanjun Su, Changli Wang, Hui Li, Xiubao Ren
JournalOncotarget (Oncotarget) Vol. 7 Issue 18 Pg. 26070-86 (May 03 2016) ISSN: 1949-2553 [Electronic] United States
PMID27036025 (Publication Type: Journal Article)
Chemical References
  • Biomarkers, Tumor
  • MicroRNAs
Topics
  • Adenocarcinoma (blood, diagnosis, genetics)
  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor (blood, genetics)
  • Case-Control Studies
  • Early Detection of Cancer
  • Female
  • Follow-Up Studies
  • Humans
  • Lung Neoplasms (blood, diagnosis, genetics)
  • Male
  • MicroRNAs (blood, genetics)
  • Middle Aged
  • Prognosis
  • Survival Rate
  • Young Adult

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