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Cryptotanshinone sensitizes antitumor effect of paclitaxel on tongue squamous cell carcinoma growth by inhibiting the JAK/STAT3 signaling pathway.

Abstract
Cryptotanshinone, a natural compound isolated from the roots of Salvia miltiorrhiza Bge (Danshen), has been found to induce cancer cells apoptosis and impair cell migration and invasion in various malignancies, but its antiproliferation and chemosensitization effects of Cryptotanshinone on tongue squamous cell carcinoma(TSCC)still remain fully elucidated. In this study, the effects of Cryptotanshinone on the proliferation, apoptosis and cell cycle of human TSCC cells, including CAL 27 and SCC 9 cells, were measured. The results demonstrated that Cryptotanshinone dose-dependently inhibited cell migration and proliferation, and induced apoptosis in TSCC cells. Mechanistic study revealed that Cryptotanshinone suppressed the expression of p-STAT3, Bcl-2, CDK2, Snail and MMP2, and induced the expression of E-cadherin, P53, P21 and β-catenin. Furthermore, we found that the combination treatment of Cryptotanshinone and paclitaxel more effectively inhibited TSCC cell proliferation and migration, and induced apoptosis via the inhibition of STAT3 signaling pathway. In brief, we provided the new evidence that Cryptotanshinone could enhance the efficacy of paclitaxel on TSCC cells in vitro and demonstrated that STAT3 signaling pathway played an important role in Cryptotanshinone-induced anticancer effects in human TSCC.
AuthorsYing Wang, Hui-Lan Lu, Yong-Dong Liu, Li-Yun Yang, Qing-Kun Jiang, Xiao-Jun Zhu, Hua-Nan Fan, Yong Qian
JournalBiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie (Biomed Pharmacother) Vol. 95 Pg. 1388-1396 (Nov 2017) ISSN: 1950-6007 [Electronic] France
PMID28946186 (Publication Type: Journal Article)
CopyrightCopyright © 2017 Elsevier Masson SAS. All rights reserved.
Chemical References
  • Antineoplastic Agents
  • Phenanthrenes
  • STAT3 Transcription Factor
  • cryptotanshinone
  • Janus Kinases
  • Paclitaxel
Topics
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (drug effects)
  • Carcinoma, Squamous Cell (pathology)
  • Cell Cycle Checkpoints (drug effects)
  • Cell Movement (drug effects)
  • Cell Proliferation (drug effects)
  • Epithelial-Mesenchymal Transition (drug effects)
  • Humans
  • Janus Kinases (metabolism)
  • Models, Biological
  • Neoplasm Invasiveness
  • Paclitaxel (pharmacology)
  • Phenanthrenes (pharmacology)
  • STAT3 Transcription Factor (metabolism)
  • Signal Transduction (drug effects)
  • Tongue Neoplasms (pathology)

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