AaHIV a sodium channel scorpion toxin inhibits the proliferation of DU145 prostate cancer cells.


Journal

Biochemical and biophysical research communications
ISSN: 1090-2104
Titre abrégé: Biochem Biophys Res Commun
Pays: United States
ID NLM: 0372516

Informations de publication

Date de publication:
08 01 2020
Historique:
received: 26 09 2019
accepted: 13 10 2019
pubmed: 2 11 2019
medline: 28 7 2020
entrez: 1 11 2019
Statut: ppublish

Résumé

Prostate cancer is the most highly diagnosed cancer in men worldwide. It is characterized by high proliferation, great invasion and metastatic potential. Sodium channel subtypes have been identified as highly expressed in different prostate cancer cell lines. In this study, we have screened the negatively charged fractions of Androctonus australis (Aa) scorpion venom to identify active peptides on DU145 prostate cancer cells proliferation. The most active compound was identified to be the sodium channel peptide AaHIV with an IC

Identifiants

pubmed: 31668811
pii: S0006-291X(19)32017-0
doi: 10.1016/j.bbrc.2019.10.115
pii:
doi:

Substances chimiques

NAV1.6 Voltage-Gated Sodium Channel 0
Scorpion Venoms 0
Sodium Channels 0
scorpion toxin AaHIV 0
scorpion toxin I, Androctonus 12584-90-6
scorpion toxin II, Androctonus 37309-04-9

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

340-346

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Rym BenAissa (R)

Université de Tunis El Manar, Institut Pasteur de Tunis, LR11IPT08 Venins et Biomolécules Thérapeutiques, 1002, Tunis, Tunisia.

Houcemeddine Othman (H)

Université de Tunis El Manar, Institut Pasteur de Tunis, LR11IPT08 Venins et Biomolécules Thérapeutiques, 1002, Tunis, Tunisia.

Claude Villard (C)

CNRS-UMR 7051, Institut de Neuro Physiopathologie (INP), Université Aix-Marseille, 27 Bd Jean Moulin, 13385, Marseille, Cedex 5, France.

Steve Peigneur (S)

Toxicology and Pharmacology, KU Leuven, Campus Gasthuisberg, O & N2, Herestraat 49, P.O. Box 922, 3000, Leuven, Belgium.

Saoussen Mlayah-Bellalouna (S)

Université de Tunis El Manar, Institut Pasteur de Tunis, LR11IPT08 Venins et Biomolécules Thérapeutiques, 1002, Tunis, Tunisia.

Zaineb Abdelkafi-Koubaa (Z)

Université de Tunis El Manar, Institut Pasteur de Tunis, LR11IPT08 Venins et Biomolécules Thérapeutiques, 1002, Tunis, Tunisia.

Naziha Marrakchi (N)

Université de Tunis El Manar, Institut Pasteur de Tunis, LR11IPT08 Venins et Biomolécules Thérapeutiques, 1002, Tunis, Tunisia.

Khadija Essafi-Benkhadir (K)

Université de Tunis El Manar, Institut Pasteur de Tunis, LR11IPT04 Epidémiologie Moléculaire et Pathologie Expérimentale Appliquée Aux Maladies Infectieuses, 1002, Tunis, Tunisia.

Jan Tytgat (J)

Toxicology and Pharmacology, KU Leuven, Campus Gasthuisberg, O & N2, Herestraat 49, P.O. Box 922, 3000, Leuven, Belgium.

José Luis (J)

CNRS-UMR 7051, Institut de Neuro Physiopathologie (INP), Université Aix-Marseille, 27 Bd Jean Moulin, 13385, Marseille, Cedex 5, France.

Najet Srairi-Abid (N)

Université de Tunis El Manar, Institut Pasteur de Tunis, LR11IPT08 Venins et Biomolécules Thérapeutiques, 1002, Tunis, Tunisia. Electronic address: najet.abid@pasteur.rns.tn.

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Classifications MeSH