Abstract | OBJECTIVE: METHODOLOGY: We used CCK8 and flow cytometry to study the growth and apoptosis. Transwell assay was used to assess invasion; wound-healing assay to assess migration; and colony formation assays to test the ability of cells to form colonies. H19, miR-675-5p, and CDH1 expressions were analyzed by qPCR. E-cadherin expression was detected using western blot. CRISPR/cas9 system was used for CDH1 knockout. RESULTS:
Ginsenoside Rd inhibited the growth and increased the apoptosis of SCC9 cells. Ginsenoside Rd also inhibited the migration and invasion of SCC9 cells. H19 and miR-675-5p were highly expressed, while CDH1 and E-cadherin expressions were low. H19 and miR-675-5p promoted SCC9 metastasis. In contrast, CDH1 and E-cadherin inhibited the metastasis of SCC9 cells. Bioinformatics analysis showed that miR-675-5p was associated with CDH1. H19 and miR-675-5p expressions decreased after ginsenoside Rd treatment, while CDH1 and E-cadherin expressions increased. CONCLUSIONS:
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Authors | Lu Chang, Dongxu Wang, Shaoning Kan, Ming Hao, Huimin Liu, Zhijing Yang, Qianyun Xia, Weiwei Liu |
Journal | Journal of applied oral science : revista FOB
(J Appl Oral Sci)
Vol. 30
Pg. e20220144
( 2022)
ISSN: 1678-7765 [Electronic] Brazil |
PMID | 36074434
(Publication Type: Journal Article)
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Chemical References |
- Antigens, CD
- CDH1 protein, human
- Cadherins
- Ginsenosides
- Histones
- MIRN675 microRNA, human
- MicroRNAs
- RNA, Long Noncoding
- ginsenoside Rd
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Topics |
- Antigens, CD
(pharmacology)
- Cadherins
- Carcinoma, Squamous Cell
- Cell Line, Tumor
- Cell Movement
- Cell Proliferation
- Ginsenosides
- Histones
(metabolism)
- Humans
- MicroRNAs
(genetics)
- RNA, Long Noncoding
(genetics, metabolism, pharmacology)
- Tongue
(metabolism)
- Tongue Neoplasms
(drug therapy)
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