HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Suppression of Dicer increases sensitivity to gefitinib in human lung cancer cells.

AbstractBACKGROUND:
Accumulating evidence is revealing an important role of microRNA (miRNA) in tumor progression and chemotherapeutic resistance. Dicer is a cytoplasmic endoribonuclease type III crucial for production of mature miRNAs. The aberrant expression of Dicer has also been reportedly associated with clinical aggressiveness, prognosis, and patient survival in various cancer types. However, the molecular mechanisms of Dicer in acquired gefitinib resistance are still not clear.
METHODS:
In this study, we analyzed the protein level of Dicer between gefitinib-sensitive (PC9) and gefitinib-resistant (PC9/GR) non-small-cell lung cancer (NSCLC) cell lines by Western blot analysis. Silence and overexpression of the Dicer were performed to investigate the effects on gefitinib sensitivity, as assessed by (3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide) assay and sub-G1 assay of flow cytometry. To further explore the mechanism of chemoresistance, we examined whether Dicer knockdown led to modulating specific miRNAs and its miRNA target genes.
RESULTS:
Dicer expression was significantly increased in PC9/GR compared with PC9 cells. Knockdown of Dicer restores gefitinib sensitivity in resistant cells, and overexpression of Dicer enhances resistance to gefitinib in sensitive cells. Silencing of Dicer induces sensitivity to gefitinib in NSCLC cells through the downregulation of miR-30b/c and miR-221/222 to increase the protein level of caspase-3, resulting in an increase in gefitinib-induced apoptosis.
CONCLUSIONS:
Dicer contributes to the resistance to gefitinib in lung cancer. These results indicate that Dicer may be a target for diagnosis and therapy of patients with resistance to gefitinib.
AuthorsJui-Chieh Chen, Yen-Hao Su, Ching-Feng Chiu, Yi-Wen Chang, Yang-Hao Yu, Chi-Feng Tseng, Hsin-An Chen, Jen-Liang Su
JournalAnnals of surgical oncology (Ann Surg Oncol) Vol. 21 Suppl 4 Pg. S555-63 (Dec 2014) ISSN: 1534-4681 [Electronic] United States
PMID24723223 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • MIRN221 microRNA, human
  • MIRN222 microRNA, human
  • MIRN30b microRNA, human
  • MicroRNAs
  • Quinazolines
  • RNA, Messenger
  • Ribonuclease III
  • Caspase 3
  • Gefitinib
Topics
  • Adenocarcinoma (drug therapy, enzymology, genetics)
  • Aged
  • Aged, 80 and over
  • Antineoplastic Agents (therapeutic use)
  • Apoptosis
  • Carcinoma, Non-Small-Cell Lung (drug therapy, enzymology, genetics)
  • Caspase 3 (metabolism)
  • Cell Line, Tumor
  • Down-Regulation
  • Drug Resistance, Neoplasm
  • Female
  • Gefitinib
  • Gene Expression
  • Gene Knockdown Techniques
  • Humans
  • Lung Neoplasms (drug therapy, enzymology, genetics)
  • Male
  • MicroRNAs (metabolism)
  • Middle Aged
  • Quinazolines (therapeutic use)
  • RNA, Messenger (metabolism)
  • Retrospective Studies
  • Ribonuclease III (genetics, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: