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Ginsenoside Rd inhibits migration and invasion of tongue cancer cells through H19/miR-675-5p/CDH1 axis.

AbstractOBJECTIVE:
Tongue squamous cell carcinoma (TSCC) is an oral cancer, with high malignancy and frequent early migration and invasion. Only a few drugs can treat tongue cancer. Ginsenoside Rd is a ginseng extract with anti-cancer effects. Many noncoding RNAs are abnormally expressed in tongue cancer, thus influencing its occurrence and development. H19 and miR-675-5p can promote cancer cell growth. This study aimed to analyze the regulation effect of ginsenoside Rd on H19 and miR-675-5p in tongue cancer.
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:
Ginsenoside Rd inhibits tongue cancer cell migration and invasion via the H19/miR-675-5p/CDH1 axis.
AuthorsLu Chang, Dongxu Wang, Shaoning Kan, Ming Hao, Huimin Liu, Zhijing Yang, Qianyun Xia, Weiwei Liu
JournalJournal of applied oral science : revista FOB (J Appl Oral Sci) Vol. 30 Pg. e20220144 ( 2022) ISSN: 1678-7765 [Electronic] Brazil
PMID36074434 (Publication Type: Journal Article)
Chemical References
  • Antigens, CD
  • CDH1 protein, human
  • Cadherins
  • Ginsenosides
  • Histones
  • MIRN675 microRNA, human
  • MicroRNAs
  • RNA, Long Noncoding
  • ginsenoside Rd
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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