Abstract | BACKGROUND: METHODS: The transcription and protein expression of BDH2 in NPC were determined by both real-time RT-PCR and immunohistochemistry staining assays. Cell proliferation, migration and invasion were evaluated by MTT assay, wound-healing assay and Transwell assay, respectively. The profile of genes regulated by restoring BDH2 expression in NPC cells was analysed by cDNA microarray. The level of iron in NPC cells was detected by iron colorimetric assay. RESULTS: The expression of BDH2 was significantly downregulated in NPC. Ectopic expression of BDH2 inhibited NPC cell proliferation and colony formation. Meanwhile, BDH2 suppressed the migration and invasion of NPC cells by reversing the epithelial-mesenchymal transition (EMT). In addition, a higher level of BDH2 decreased the growth and metastasis of NPC cells via reducing intracellular iron level. CONCLUSIONS: Our findings suggest that BDH2 may be a candidate tumour-suppressor gene in NPC. Decreasing intracellular iron could be an effective therapeutic approach for NPC.
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Authors | Bo Li, Zhipeng Liao, Yingxi Mo, Weilin Zhao, Xiaohui Zhou, Xiling Xiao, Wanmeng Cui, Guofei Feng, Suhua Zhong, Yushan Liang, Chunping Du, Guangwu Huang, Ping Li, Xue Xiao, Xiaoying Zhou, Rensheng Wang, Zhe Zhang |
Journal | British journal of cancer
(Br J Cancer)
Vol. 122
Issue 1
Pg. 102-110
(01 2020)
ISSN: 1532-1827 [Electronic] England |
PMID | 31819181
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Iron
- BDH2 protein, human
- Hydroxybutyrate Dehydrogenase
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Topics |
- Animals
- Cell Line, Tumor
- Cell Movement
(genetics)
- Cell Proliferation
(genetics)
- Down-Regulation
- Epithelial-Mesenchymal Transition
(genetics)
- Gene Expression Regulation, Neoplastic
- Heterografts
- Humans
- Hydroxybutyrate Dehydrogenase
(genetics, metabolism)
- Iron
(metabolism)
- Male
- Mice
- Mice, Inbred BALB C
- Mice, Nude
- Nasopharyngeal Carcinoma
(metabolism, pathology)
- Nasopharyngeal Neoplasms
(metabolism, pathology)
- Transfection
- Tumor Burden
(genetics)
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