Abstract | PURPOSE: MATERIALS AND METHODS: The effect of NIM on Hep-2 cell proliferation was measured by the MTT assay. Flow cytometry was used to evaluate the cell cycle and apoptosis in Hep-2 cells. A Western blot analysis was used to detect changes in the protein expression levels of COX-2, Survivin and proliferating cell nuclear antigen ( PCNA) in Hep-2 cells. A Hep-2 tumor xenograft model was established in nude mice to observe tumor growth. The changes in the xenograft tumors were observed after hematoxylin/ eosin staining. The expression levels of COX-2, Survivin and PCNA proteins and mRNA were measured by immunohistochemical analysis and RT-PCR, respectively. RESULTS: NIM had time- and dose-dependent inhibitory effect on the proliferation of Hep-2 cells. NIM could prevent the progression of the cell cycle. After NIM treatment, COX-2, Survivin and PCNA protein levels were reduced in the Hep-2 cells. The volume and weight of the xenograft tumors in the NIM treatment group were significantly reduced. The NIM treatment group also exhibited significantly reduced expression levels of COX-2, Survivin and PCNA at both the protein and mRNA levels. CONCLUSIONS:
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Authors | Zhuoping Liang, Jinbo Liu, Leiji Li, Haiyang Wang, Chong Zhao, Liang Jiang, Gang Qin |
Journal | American journal of otolaryngology
(Am J Otolaryngol)
2014 Mar-Apr
Vol. 35
Issue 2
Pg. 120-9
ISSN: 1532-818X [Electronic] United States |
PMID | 24321753
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2014. |
Chemical References |
- Birc5 protein, mouse
- Cyclooxygenase Inhibitors
- Inhibitor of Apoptosis Proteins
- Platelet Aggregation Inhibitors
- Proliferating Cell Nuclear Antigen
- RNA, Messenger
- Repressor Proteins
- Sulfonamides
- Survivin
- Ptgs2 protein, mouse
- Cyclooxygenase 2
- nimesulide
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Topics |
- Animals
- Apoptosis
(drug effects)
- Blotting, Western
- Carcinoma, Squamous Cell
(drug therapy, genetics, pathology)
- Cell Cycle
(drug effects)
- Cell Line, Tumor
- Cell Proliferation
- Cyclooxygenase 2
(biosynthesis, genetics)
- Cyclooxygenase Inhibitors
(pharmacology)
- Flow Cytometry
- Gene Expression Regulation, Neoplastic
(drug effects)
- Humans
- Immunohistochemistry
- Inhibitor of Apoptosis Proteins
(biosynthesis, genetics)
- Laryngeal Neoplasms
(drug therapy, genetics, pathology)
- Mice
- Mice, Inbred BALB C
- Neoplasms, Experimental
(drug therapy, genetics, pathology)
- Platelet Aggregation Inhibitors
- Proliferating Cell Nuclear Antigen
(biosynthesis, genetics)
- RNA, Messenger
(genetics)
- Real-Time Polymerase Chain Reaction
- Repressor Proteins
(biosynthesis, genetics)
- Sulfonamides
(pharmacology)
- Survivin
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