HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Physciosporin suppresses the proliferation, motility and tumourigenesis of colorectal cancer cells.

AbstractBACKGROUND:
Lichens, which represent symbiotic associations of fungi and algae, are potential sources of numerous natural products. Physciosporin (PHY) is a potent secondary metabolite found in lichens and was recently reported to inhibit the motility of lung cancer cells via novel mechanisms.
PURPOSE:
The present study investigated the anticancer potential of PHY on colorectal cancer (CRC) cells.
METHODS:
PHY was isolated from lichen extract by preparative TLC. The effect of PHY on cell viability, motility and tumourigenicity was elucidated by MTT assay, hoechst staining, flow cytometric analysis, transwell invasion and migration assay, soft agar colony formation assay, Western blotting, qRT-PCR and PCR array in vitro as well as tumorigenicity study in vivo.
RESULTS:
PHY decreased the viability of various CRC cell lines (Caco2, CT26, DLD1, HCT116 and SW620). Moreover, PHY elicited cytotoxic effects by inducing apoptosis at toxic concentrations. At non-toxic concentrations, PHY dose-dependently suppressed the invasion, migration and colony formation of CRC cells. PHY inhibited the motility of CRC cells by suppressing epithelial-mesenchymal transition and downregulating actin-based motility markers. In addition, PHY downregulated β-catenin and its downstream target genes cyclin-D1 and c-Myc. Moreover, PHY modulated KAI1 C-terminal-interacting tetraspanin and KAI1 expression, and downregulated the downstream transcription factors c-jun and c-fos. Finally, PHY administration showed considerable bioavailability and effectively decreased the growth of CRC xenografts in mice without causing toxicity.
CONCLUSION:
PHY suppresses the growth and motility of CRC cells via novel mechanisms.
Authorsİsa Taş, Jin Han, So-Yeon Park, Yi Yang, Rui Zhou, Chathurika D B Gamage, Tru Van Nguyen, Ji-Yoon Lee, Yong Jae Choi, Young Hyun Yu, Kyung-Sub Moon, Kyung Keun Kim, Hyung-Ho Ha, Sang Kyum Kim, Jae-Seoun Hur, Hangun Kim
JournalPhytomedicine : international journal of phytotherapy and phytopharmacology (Phytomedicine) Vol. 56 Pg. 10-20 (Mar 15 2019) ISSN: 1618-095X [Electronic] Germany
PMID30668330 (Publication Type: Journal Article)
CopyrightCopyright © 2018 Elsevier GmbH. All rights reserved.
Chemical References
  • Antineoplastic Agents
  • CTNNB1 protein, human
  • Oxepins
  • beta Catenin
  • physciosporin
Topics
  • Animals
  • Antineoplastic Agents (administration & dosage, pharmacokinetics, pharmacology)
  • Apoptosis (drug effects)
  • Cell Line, Tumor
  • Cell Movement (drug effects)
  • Cell Proliferation (drug effects)
  • Cell Survival (drug effects)
  • Cell Transformation, Neoplastic (genetics)
  • Colorectal Neoplasms (drug therapy, pathology)
  • Dose-Response Relationship, Drug
  • Drug Screening Assays, Antitumor
  • Epithelial-Mesenchymal Transition (drug effects)
  • Gene Expression Regulation, Neoplastic (drug effects)
  • Humans
  • Lichens (chemistry)
  • Male
  • Mice, Inbred BALB C
  • Oxepins (administration & dosage, pharmacokinetics, pharmacology)
  • Xenograft Model Antitumor Assays
  • beta Catenin (genetics, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: