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Modulating effect of Coronarin D in 5-fluorouracil resistance human oral cancer cell lines induced apoptosis and cell cycle arrest through JNK1/2 signaling pathway.

Abstract
Coronarin D (CD) is one of the main components of Hedychium coronarium rhizome, which has therapeutic potential by reducing cell proliferation in cancer cells. However, the mechanism of CD to 5-fluorouracil (5FU) oral cancer cell remain unclearly. This study discusses the CD to 5FU chemoresistance oral squamous cell carcinoma (OSCC) biochemical mechanisms and possibly pathways to inhibit multiplication in oral cancer. The effect of CD-treated 5FU-chemoresistance human oral cancer cell lines were subjected to MTT assay, cell cycle assay, DAPI assay, annexin-V/PI double staining assay and mitochondrial membrane potential measurement. Furthermore, western blotting was performed to assess the effect of CD on the expression levels of apoptosis related protein and MAPK signaling pathway. The results of the study evidenced that CD reduced viability of 5FU cancer cells in a dose- and time-dependent manner compared with control. The cytotoxic effect of CD lead to cell cycle arrest in the G2/M phase and induced apoptosis in both internal and external pathways. CD induces apoptosis by enhancing phosphorylation of JNK, further exploring the combination of CD and SP600125 reduced the overexpression of phosphate JNK levels. The mechanism of action of CD in 5FU on human oral cancer cells is reported for the first time and can hopeful to be a potential therapeutic agent for 5FU against human oral cancer cells.
AuthorsMing-Yu Hsieh, Ming-Ju Hsieh, Yu-Sheng Lo, Chia-Chieh Lin, Yi-Ching Chuang, Mu-Kuan Chen, Ming-Chih Chou
JournalBiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie (Biomed Pharmacother) Vol. 128 Pg. 110318 (Aug 2020) ISSN: 1950-6007 [Electronic] France
PMID32502840 (Publication Type: Journal Article)
CopyrightCopyright © 2020 The Author(s). Published by Elsevier Masson SAS.. All rights reserved.
Chemical References
  • Antimetabolites, Antineoplastic
  • Diterpenes
  • coronarin D
  • Mitogen-Activated Protein Kinase 9
  • Mitogen-Activated Protein Kinase 8
  • Fluorouracil
Topics
  • Antimetabolites, Antineoplastic (pharmacology)
  • Apoptosis (drug effects)
  • Cell Cycle Checkpoints (drug effects)
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • Diterpenes (pharmacology)
  • Dose-Response Relationship, Drug
  • Drug Resistance, Neoplasm (drug effects)
  • Fluorouracil (pharmacology)
  • Humans
  • Mitogen-Activated Protein Kinase 8 (metabolism)
  • Mitogen-Activated Protein Kinase 9 (metabolism)
  • Phosphorylation
  • Signal Transduction
  • Squamous Cell Carcinoma of Head and Neck (drug therapy, enzymology, pathology)
  • Time Factors
  • Tongue Neoplasms (drug therapy, enzymology, pathology)

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