Abstract | BACKGROUND: METHODS: The gene expression levels of ABAT and ALDH6A1 in ccRCC were analyzed from gene expression microarray datasets and RNA sequencing data. Clinical information was analyzed from The Cancer Genome Atlas (TCGA) data. The distributions of ABAT and ALDH6A1 in ccRCC clinical tissues were screened by reverse transcription-quantitative polymerase chain reaction (RT-QPCR) and immunohistochemical assays. The effect of overexpression of ABAT or ALDH6A1 was measured by detecting the cell viability, migration ability, and the ratio of lactate and nicotinamide adenine dinucleotide phosphate ( NADPH). Chromatin immunoprecipitation (ChIP) and luciferase reporter assays were carried out to investigate the transcript regulation of HNF4A in ABAT and ALDH6A1. RESULTS: Remarkable downregulated ABAT and ALDH6A1 expression levels were observed in ccRCC patients and low expression of ABAT and ALDH6A1 was correlated with poor survival. Overexpression of ABAT or ALDH6A1 significantly attenuated cell proliferation and migration, and impaired lactate production. In ABAT increased ccRCC cells, the ratio of NADPH/NADP+ was reduced. Finally, we demonstrated that ABAT and ALDH6A1 were directly regulated by a tumor suppressor, HNF4A. CONCLUSIONS: These observations identified HNF4A-regulated low-expressed ABAT and ALDH6A1 as promising diagnostic and prognostic biomarkers for ccRCC.
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Authors | Jun Lu, Zhan Chen, Hu Zhao, Huiyue Dong, Ling Zhu, Yi Zhang, Jie Wang, Hehuan Zhu, Qiang Cui, Chuang Qi, Shuiliang Wang, Shushang Chen, Jichun Shao |
Journal | Journal of translational medicine
(J Transl Med)
Vol. 18
Issue 1
Pg. 101
(02 24 2020)
ISSN: 1479-5876 [Electronic] England |
PMID | 32093682
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- HNF4A protein, human
- Hepatocyte Nuclear Factor 4
- Transcription Factors
- Aldehyde Oxidoreductases
- ALDH6A1 protein, human
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Topics |
- Aldehyde Oxidoreductases
- Carcinoma, Renal Cell
(genetics)
- Cell Line, Tumor
- Cell Proliferation
- Gene Expression Regulation, Neoplastic
- Hepatocyte Nuclear Factor 4
- Humans
- Kidney Neoplasms
(genetics)
- Transcription Factors
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