Naja ashei venom induces mitochondria-mediated apoptosis in human colorectal cancer cells.
Animals
Apoptosis
/ drug effects
Apoptosis Regulatory Proteins
/ metabolism
Caspase 3
/ metabolism
Caspase 9
/ metabolism
Cell Cycle Checkpoints
/ drug effects
Cell Proliferation
/ drug effects
Cell Survival
/ drug effects
Colorectal Neoplasms
/ drug therapy
HCT116 Cells
Humans
Membrane Potential, Mitochondrial
/ drug effects
Mitochondria
/ metabolism
Mitochondrial Proteins
/ metabolism
Naja
Phosphorylation
/ drug effects
Proto-Oncogene Proteins c-bcl-2
/ metabolism
Signal Transduction
/ drug effects
Venoms
/ pharmacology
Journal
Acta biochimica Polonica
ISSN: 1734-154X
Titre abrégé: Acta Biochim Pol
Pays: Poland
ID NLM: 14520300R
Informations de publication
Date de publication:
07 Jun 2019
07 Jun 2019
Historique:
received:
15
02
2019
accepted:
26
04
2019
pubmed:
8
6
2019
medline:
18
12
2019
entrez:
8
6
2019
Statut:
ppublish
Résumé
In the present study, we investigated the antiproliferative activity of Naja ashei full venom (NAV) on human colorectal cancer cells. The NAV-induced antiproliferative effect was associated with cell cycle arrest in S phase and increased number of cells with sub G0/G1 DNA content, which is considered a marker of apoptosis. Apoptosis has also been confirmed with annexin V/PI staining. Furthermore, flow cytometric analysis revealed loss of mitochondrial membrane potential with concomitant increase in cytochrome c and Smac/DIABLO protein content. These effects were associated with the activation of caspase-9 and caspase-3, as well as with PARP cleavage. Moreover, phosphorylation of antiapoptotic Bcl-2 protein in NAV-treated HCT116 was observed. In conclusion, our study for the first time documented antiproliferative/pro-apoptotic effect of NAV in colorectal cancer cells. Our results strongly suggest the involvement of mitochondria in NAV induced apoptosis of cancer cells. Future studies are needed to further examine the potential of NAV in the treatment of colon cancer.
Identifiants
pubmed: 31172986
pii: 2779
doi: 10.18388/abp.2018_2779
doi:
Substances chimiques
Apoptosis Regulatory Proteins
0
BCL2 protein, human
0
DIABLO protein, human
0
Mitochondrial Proteins
0
Proto-Oncogene Proteins c-bcl-2
0
Venoms
0
CASP3 protein, human
EC 3.4.22.-
CASP9 protein, human
EC 3.4.22.-
Caspase 3
EC 3.4.22.-
Caspase 9
EC 3.4.22.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM