Knocking down CDK4 mediates the elevation of let-7c suppressing cell growth in nasopharyngeal carcinoma
Creators
- 1. Cancer Research Institute, Southern Medical University, Guangzhou 510515 (China)
- 2. Department of Pathology, Guangzhou Medical University, Guangzhou 510182 (China)
- 3. Pediatric Center of Zhujiang Hospital, Southern Medical University, Guangzhou 510282 PR (China)
- 4. Otorhinolaryngology of Zhujiang Hospital, Southern Medical University, Guangzhou 510282 PR (China)
- 5. Cancer Center of Affiliated Hospital, Guangdong Medical College, Zhanjiang 524001 PR (China)
- 6. Tumor Center of Integrated Chinese and Western medicine Hospital, Southern Medical University, Guangzhou 510315 PR (China)
Description
CDK4 is a protein kinase in the CDK family important for G1/S phase cell cycle progression. However, the roles and molecular mechanisms of CDK4 triggering nasopharynx carcinogenesis are still unclear. Lentiviral-vector mediated shRNA was used to suppress CDK4 expression and examine its molecular mechanisms. Using immunohistochemistry, we analyzed CDK4 protein expression in clinicopathologically characterized nasopharyngeal carcinoma (NPC) cases and nasopharyngeal tissues (NPs). Survival curves were plotted by the Kaplan-Meier method and compared using the log-rank test. In this investigation, we knocked down CDK4 expression and observed that NPC cell growth and cell cycle progression were significantly blocked by suppressing expression of CCND1, CDK6, and E2F1 as well as elevated p21 expression. Further, we found that reduced CDK4 expression elevated the expression of let-7c, a tumor-suppressive miRNA modulated by E2F1. We found that let-7c was markedly downregulated in NPC tissues compared to NPs and suppressed cell growth and cell cycle progression by modulating p15/p16/CDK4/E2F1 pathway. Finally, CDK4 protein was observed to be overexpressed in NPC tissues and could be considered an unfavorable prognosis factor for NPC patients although its independent prognostic value did not reach statistical significance (p = 0.087). Our results demonstrated that overexpressed CDK4 is an unfavorable prognostic factor which suppresses the expression of tumor suppressive-factor let-7c through p21/CCND1/CDK6/E2F1 signaling, and inhibits cell proliferation by p15/p16/CDK4/E2F1 feedback signaling in NPC
Availability note (English)
Available from http://dx.doi.org/10.1186/1471-2407-14-274; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014407Additional details
Identifiers
Publishing Information
- Journal Title
- BMC cancer (Online)
- Journal Volume
- 14
- Journal Page Range
- p. 274
- ISSN
- 1471-2407
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47000874
- Subject category
- S63: RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS; S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CARCINOMAS; CELL CYCLE; CELL PROLIFERATION; GROWTH; LEVELS; MONOCLINIC LATTICES; PHARYNX; PROTEINS; SURVIVAL CURVES
- Descriptors DEC
- BODY; CRYSTAL LATTICES; CRYSTAL STRUCTURE; DIGESTIVE SYSTEM; DISEASES; NEOPLASMS; ORGANIC COMPOUNDS; ORGANS; RESPIRATORY SYSTEM; THREE-DIMENSIONAL LATTICES
Optional Information
- Copyright
- Copyright (c) 2014 Liu et al.
- Notes
- PMCID: PMC4014407; PUBLISHER-ID: 1471-2407-14-274; PMID: 24751144; OAI: oai:pubmedcentral.nih.gov:4014407; licensee BioMed Central Ltd.