Abstract | BACKGROUNDS: METHODS: SK-N-SH and SK-N-BE cells were treated with MPP+ to establish the MPP+-stimulated cell model of PD, and MALAT1 expression was determined. Then, the effects of MALAT1 depletion on cell proliferation and apoptosis were determined in the MPP+-stimulated cell model of PD. Besides, the correlations between microRNA-135b-5p (miR-135b-5p) and MALAT1 or glycoprotein nonmetastatic melanoma protein B (GPNMB) in MPP+-stimulated cell model of PD were explored. RESULTS: MALAT1 was increasingly expressed and downregulation of MALAT1 promoted cell proliferation while inhibited apoptosis in MPP+-stimulated cells. Besides, miR-135b-5p was a target of MALAT1 and directly targeted to GPNMB. Further investigation indicated that suppression of MALAT1 regulated cell proliferation and apoptosis by miR-135b-5p/GPNMB axis. CONCLUSION: Our findings reveal that MALAT1/miR-135b-5p/GPNMB axis regulated cell proliferation and apoptosis in MPP+-stimulated cell model of PD, providing a potential biomarker and therapeutic target for PD.
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Authors | Kefeng Lv, Yuhua Liu, Yanbing Zheng, Shaowen Dai, Peifeng Yin, Haifeng Miao |
Journal | Biological research
(Biol Res)
Vol. 54
Issue 1
Pg. 10
(Mar 16 2021)
ISSN: 0717-6287 [Electronic] England |
PMID | 33726823
(Publication Type: Journal Article)
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Chemical References |
- GPNMB protein, human
- MALAT1 long non-coding RNA, human
- MIRN135 microRNA, human
- Membrane Glycoproteins
- MicroRNAs
- RNA, Long Noncoding
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Topics |
- Apoptosis
- Cell Proliferation
- Cells, Cultured
- Humans
- Membrane Glycoproteins
(genetics)
- MicroRNAs
(genetics)
- Parkinson Disease
(genetics)
- RNA, Long Noncoding
(genetics)
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