Abstract | PURPOSE: METHODS: Cal27 and hNOK cells were cultivated, real-time PCR and Western blotting were used to detect the expression of Grb7 in hNOK and Cal27. Cal27 was transfected with Grb7 siRNA for 48 h, cell proliferation was assayed using MTT. Flow cytometry was used to determine the cell cycle and apoptosis. Western blot was used to evaluate the expression of caspase3, Bax, bcl-2, Cyclin D1, Rb, E2F1, ERK and FOXM1. Grb7 siRNA and negative control were designed and injected subcutaneously into the mice, tumor volume and weight were measured. Statistical analysis was performed using SPSS 11.0 software package. RESULTS: Grb7 was highly expressed in Cal27 compared with hNOK. Depletion of Grb7 significantly inhibited cell proliferation, blocked G1/S phase transition, promoted cell apoptosis. Knockdown of Grb7 suppressed the expression of Cyclin D1 and Rb, upregulated E2F1 expression. Moreover, c- caspase 3 and Bax was also reduced after inhibition of Grb7. ERK/FOXM1 signaling pathway was also inhibited by Grb7. In addition, the volume and weight of tumor xenografts were reduced by siGrb7. CONCLUSIONS: Depletion of Grb7 inhibits cell proliferation, promotes apoptosis and reduces tumor xenografts through ERK/FOXM1 pathway.
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Authors | Bing-Yao Liu, Gang Cao, Zhen Dong, Wei Chen, Jin-Ke Xu, Sen-Lin Zhang, Zhi-Qiang Weng |
Journal | Shanghai kou qiang yi xue = Shanghai journal of stomatology
(Shanghai Kou Qiang Yi Xue)
Vol. 25
Issue 6
Pg. 688-693
(Dec 2016)
ISSN: 1006-7248 [Print] China |
PMID | 28275791
(Publication Type: Journal Article)
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Chemical References |
- Apoptosis Regulatory Proteins
- CCND1 protein, human
- RNA, Small Interfering
- Cyclin D1
- GRB7 Adaptor Protein
- Caspase 3
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Topics |
- Animals
- Apoptosis
- Apoptosis Regulatory Proteins
- Carcinoma, Squamous Cell
(metabolism)
- Caspase 3
- Cell Cycle
- Cell Line, Tumor
- Cell Proliferation
(physiology)
- Cyclin D1
- GRB7 Adaptor Protein
(genetics, metabolism)
- Gene Knockdown Techniques
- Humans
- MAP Kinase Signaling System
- Mice
- Mouth Neoplasms
(metabolism)
- RNA, Small Interfering
- Real-Time Polymerase Chain Reaction
- Signal Transduction
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