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Shikonin as an inhibitor of the LPS-induced epithelial-to-mesenchymal transition in human breast cancer cells.

Abstract
Shikonin (SK), a natural naphthoquinone isolated from the Chinese medicinal herb, has been known to suppress the proliferation of several cancer cells. However, its role in the epithelial mesenchymal transition (EMT) has yet to be demonstrated. The aim of the present study was to examine the effects of SK on EMT. Lipopolysaccharide (LPS) induced EMT-like phenotypic changes, enhancing cell migration and invasion. SK markedly reduced the expression of the LPS-induced EMT markers, including N-cadherin in MDA-MB‑231 cells, and increased the expression of E-cadherin in MCF-7 cells. SK also inhibited cell migration and invasion in vitro. The effects of SK on the LPS-induced EMT were mediated by the inactivation of the NF-κB-Snail signaling pathway. The results provided new evidence that SK suppresses breast cancer cell invasion and migration by inhibiting the EMT. Therefore, SK is a potentially effective anticancer agent for breast tumors, by inhibiting metastasis.
AuthorsDarong Hong, Soon Young Jang, Eun Hyang Jang, Bom Jung, In-Hye Cho, Min-Ju Park, Seo Young Jeong, Jong-Ho Kim
JournalInternational journal of molecular medicine (Int J Mol Med) Vol. 36 Issue 6 Pg. 1601-6 (Dec 2015) ISSN: 1791-244X [Electronic] Greece
PMID26498588 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anti-Inflammatory Agents, Non-Steroidal
  • Cadherins
  • Drugs, Chinese Herbal
  • Lipopolysaccharides
  • Naphthoquinones
  • Snail Family Transcription Factors
  • Transcription Factor RelA
  • Transcription Factors
  • shikonin
Topics
  • Anti-Inflammatory Agents, Non-Steroidal (pharmacology)
  • Blotting, Western
  • Breast Neoplasms (metabolism, pathology)
  • Cadherins (metabolism)
  • Cell Line, Tumor
  • Cell Movement (drug effects)
  • Cell Proliferation (drug effects)
  • Cell Survival (drug effects)
  • Dose-Response Relationship, Drug
  • Drugs, Chinese Herbal (pharmacology)
  • Epithelial-Mesenchymal Transition (drug effects)
  • Female
  • Humans
  • Lipopolysaccharides (pharmacology)
  • MCF-7 Cells
  • Microscopy, Fluorescence
  • Naphthoquinones (pharmacology)
  • Snail Family Transcription Factors
  • Transcription Factor RelA (metabolism)
  • Transcription Factors (metabolism)

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