Physciosporin suppresses the proliferation, motility and tumourigenesis of colorectal cancer cells
(2019) In Phytomedicine 56. p.10-20- Abstract
BACKGROUND: 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... (More)
BACKGROUND: 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.
(Less)
- author
- publishing date
- 2019-03-15
- type
- Contribution to journal
- publication status
- published
- keywords
- Animals, Antineoplastic Agents/administration & dosage, 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, 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, Xenograft Model Antitumor Assays, beta Catenin/genetics
- in
- Phytomedicine
- volume
- 56
- pages
- 10 - 20
- publisher
- Urban & Fischer Verlag
- external identifiers
-
- scopus:85056248898
- pmid:30668330
- ISSN
- 0944-7113
- DOI
- 10.1016/j.phymed.2018.09.219
- language
- English
- LU publication?
- no
- additional info
- Copyright © 2018 Elsevier GmbH. All rights reserved.
- id
- 8d48aae0-0b42-45a0-92d7-bad32d745408
- date added to LUP
- 2022-08-25 14:34:33
- date last changed
- 2024-08-07 20:53:05
@article{8d48aae0-0b42-45a0-92d7-bad32d745408, abstract = {{<p>BACKGROUND: 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.</p><p>PURPOSE: The present study investigated the anticancer potential of PHY on colorectal cancer (CRC) cells.</p><p>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.</p><p>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.</p><p>CONCLUSION: PHY suppresses the growth and motility of CRC cells via novel mechanisms.</p>}}, author = {{Taş, İsa and Han, Jin and Park, So-Yeon and Yang, Yi and Zhou, Rui and Gamage, Chathurika D B and Van Nguyen, Tru and Lee, Ji-Yoon and Choi, Yong Jae and Yu, Young Hyun and Moon, Kyung-Sub and Kim, Kyung Keun and Ha, Hyung-Ho and Kim, Sang Kyum and Hur, Jae-Seoun and Kim, Hangun}}, issn = {{0944-7113}}, keywords = {{Animals; Antineoplastic Agents/administration & dosage; 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; 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; Xenograft Model Antitumor Assays; beta Catenin/genetics}}, language = {{eng}}, month = {{03}}, pages = {{10--20}}, publisher = {{Urban & Fischer Verlag}}, series = {{Phytomedicine}}, title = {{Physciosporin suppresses the proliferation, motility and tumourigenesis of colorectal cancer cells}}, url = {{http://dx.doi.org/10.1016/j.phymed.2018.09.219}}, doi = {{10.1016/j.phymed.2018.09.219}}, volume = {{56}}, year = {{2019}}, }