Remarkable apoptotic pathway of Hemiscorpius lepturus scorpion venom on CT26 cell line.
Animals
Apoptosis
/ drug effects
Caspase 3
/ metabolism
Cell Line, Tumor
Chlorocebus aethiops
Colonic Neoplasms
/ drug therapy
Female
Inhibitory Concentration 50
Male
Mice
Mice, Inbred BALB C
Proto-Oncogene Proteins c-bcl-2
/ metabolism
Scorpion Venoms
/ metabolism
Scorpions
Tumor Suppressor Protein p53
/ metabolism
Vero Cells
Xenograft Model Antitumor Assays
/ methods
bcl-2-Associated X Protein
/ metabolism
Antineoplastic natural compounds
Apoptosis
Colorectal cancer
Hemiscorpius lepturus
Neoplasms
Scorpion venoms
Journal
Cell biology and toxicology
ISSN: 1573-6822
Titre abrégé: Cell Biol Toxicol
Pays: Switzerland
ID NLM: 8506639
Informations de publication
Date de publication:
08 2019
08 2019
Historique:
received:
10
10
2018
accepted:
29
11
2018
pubmed:
9
1
2019
medline:
21
7
2020
entrez:
9
1
2019
Statut:
ppublish
Résumé
Scorpion venom, considered as a treasure trove of various bioactive molecules, is a new approach to induce cancer cell death via apoptosis pathways. In the present study, we evaluated for first time the anti-proliferative efficacy of Hemiscorpius lepturus scorpion venom and its pathway on a colon carcinoma cell. The CT26 and VERO cell lines were treated with various concentrations of the venom. The IC50 values were estimated by MTT assay test, and the apoptosis was evaluated by flow cytometry. Moreover, RT-PCR analysis was used to investigate the levels of Bax, Bcl2, Trp53, and Casp3 mRNA expression. The mice xenograft model was established to evaluate the therapy efficiency of venom. Some valuable exponential growth parameters were evaluated in treated mice. The scorpion venom inhibited the growth of CT26 cells with an IC50 value about 120 μg/ml. However, VERO cells increased to 896 μg/ml under the same condition. A remarkable apoptotic cells in CT26 cells were revealed by flow cytometry assay. A significant over-expression was observed in Bax, Casp3, and Trp53 and downregulated in Bcl2 mRNA level in tumor tissue after treatment with scorpion venom (p < 0.05). All changes of valuable exponential growth parameters showed a shrinking tumor size. Our findings indicated that Hemiscorpius lepturus venom has a special anti-proliferative effect on CT26 cells via Trp53/Bcl2/Casp3 pathway. Considering its powerful cytotoxic vigor against a colon cancer cell (CT26) and low toxicity to non-tumorigenic cell (VERO), we propose that this venom probably has a specific effect on other colon cancer cells and may turn out to be a novel therapeutic strategy in treating colon cancer.
Identifiants
pubmed: 30617443
doi: 10.1007/s10565-018-09455-3
pii: 10.1007/s10565-018-09455-3
doi:
Substances chimiques
Proto-Oncogene Proteins c-bcl-2
0
Scorpion Venoms
0
Tumor Suppressor Protein p53
0
bcl-2-Associated X Protein
0
Caspase 3
EC 3.4.22.-
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM