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Buddlejasaponin IV induces apoptotic cell death by activating the mitochondrial‑dependent apoptotic pathway and reducing α2β1 integrin‑mediated adhesion in HT‑29 human colorectal cancer cells

Authors
 Jin-Eun Kim  ;  Sun Kyoung Lee  ;  Junhee Park  ;  Min Ju Jung  ;  So-Eun An  ;  Hye Ji Yang  ;  Won-Yoon Chung 
Citation
 ONCOLOGY REPORTS, Vol.49(3) : 58, 2023-03 
Journal Title
ONCOLOGY REPORTS
ISSN
 1021-335X 
Issue Date
2023-03
MeSH
Animals ; Anoikis ; Apoptosis ; Caspase 3 ; Cell Adhesion ; Colonic Neoplasms* ; Focal Adhesion Protein-Tyrosine Kinases / metabolism ; HT29 Cells ; Humans ; Integrins / metabolism ; Mice ; Poly(ADP-ribose) Polymerase Inhibitors / pharmacology ; Proto-Oncogene Proteins c-akt* ; bcl-2-Associated X Protein
Keywords
Akt ; a2β1 integrin ; anoikis ; apoptosis ; buddlejasaponin IV ; cell adhesion ; focal adhesion kinase ; mitochondrial‑dependent
Abstract
Colon cancer is one of the most frequent malignant neoplasms worldwide. Epidemiological studies suggested that the development of colon cancer can be prevented by plant-derived ingredients. In the present study, the chemo- preventive activity of buddlejasaponin IV (BS-IV), isolated from the aerial part of Pleurospermum kamtschaticum, was investigated using cell viability, DNA fragmentation, caspase-3 activity, anoikis, cell adhesion, and flow cytometry assays and a murine lung metastasis model. Protein expres- sion levels were detected by western blotting. Treatment with BS-IV significantly reduced cell viability and caused DNA fragmentation in HT-29 human colorectal cancer cells. BS-IV increased the ratio of Bax to Bcl-2 by significantly inhibiting Bcl-2 expression levels. BS-IV reduced expression levels of procaspase-9, procaspase-3, and full-length poly (ADP-ribose) polymerase (PARP) and increased cleaved PARP and nonste- roidal anti-inflammatory drug activated gene-1 expression levels and caspase-3 activity. In addition, BS-IV decreased the attachment of HT-29 cells to the extracellular matrix proteins collagen type I and IV and downregulated cell surface expres- sion of α2β1 integrin by inhibiting its glycosylation. BS-IV also reduced the expression and phosphorylation levels of focal adhesion kinase (FAK) and Akt, and the reduced FAK and Akt levels were rescued by treatment with a caspase-3 inhibitor Z-VAD-FMK. Furthermore, orally administered BS-IV inhibited the formation of tumor nodules in Balb/C mice intravenously injected with CT-26 murine colorectal cancer cells. Collectively, these findings indicated that BS-IV induces apoptosis via the mitochondrial-dependent pathway by increasing the ratio of Bax to Bcl-2 and activating caspases. BS-IV also induces anoikis by inhibiting α2β1 integrin-mediated cell adhesion and signaling and inhibits the lung metastasis of colon cancer cells. Therefore, BS-IV may serve as a promising cancer chemopreventive agent. © 2023 Spandidos Publications. All rights reserved.
Full Text
https://www.spandidos-publications.com/or/49/3/58
DOI
10.3892/or.2023.8495
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers
Yonsei Authors
Park, Jun Hee(박준희)
Lee, Sun Kyoung(이선경) ORCID logo https://orcid.org/0000-0002-3707-8050
Chung, Won Yoon(정원윤) ORCID logo https://orcid.org/0000-0001-8428-9005
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/194022
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