Keyword search (3,448 papers available)


The Biology of Vasopressin.

Author(s): Sparapani S, Millet-Boureima C, Oliver J, Mu K, Hadavi P, Kalostian T, Ali N, Avelar CM, Bardies M, Barrow B, Benedikt M, Biancardi G, Bindr...

Vasopressins are evolutionarily conserved peptide hormones. Mammalian vasopressin functions systemically as an antidiuretic and regulator of blood and cardiac flow essential for adapting to terrest...

Article GUID: 33477721

Drug discovery and chemical probing in Drosophila.

Author(s): Millet-Boureima C, Selber-Hnatiw S, Gamberi C

Genome. 2020 Jun 18;: Authors: Millet-Boureima C, Selber-Hnatiw S, Gamberi C

Article GUID: 32551911

Cyst Reduction in a Polycystic Kidney Disease Drosophila Model Using Smac Mimics.

Author(s): Millet-Boureima C, Chingle R, Lubell WD, Gamberi C

Biomedicines. 2019 Oct 18;7(4): Authors: Millet-Boureima C, Chingle R, Lubell WD, Gamberi C

Article GUID: 31635379

Modeling Renal Disease "On the Fly".

Author(s): Millet-Boureima C, Porras Marroquin J, Gamberi C

Biomed Res Int. 2018;2018:5697436 Authors: Millet-Boureima C, Porras Marroquin J, Gamberi C

Article GUID: 29955604


Title:Cyst Reduction in a Polycystic Kidney Disease Drosophila Model Using Smac Mimics.
Authors:Millet-Boureima CChingle RLubell WDGamberi C
Link:https://www.ncbi.nlm.nih.gov/pubmed/31635379?dopt=Abstract
DOI:10.3390/biomedicines7040082
Category:Biomedicines
PMID:31635379
Dept Affiliation: BIOLOGY
1 Biology Department, Concordia University, Montreal, QC H4B 1R6, Canada. cassandra.millet@mail.concordia.ca.
2 Département de Chimie, Université de Montréal, Montreal, QC H3T 1J4, Canada. ramesh.chingle@nih.gov.
3 Département de Chimie, Université de Montréal, Montreal, QC H3T 1J4, Canada. lubell@chimie.umontreal.ca.
4 Biology Department, Concordia University, Montreal, QC H4B 1R6, Canada. chiara.gamberi@concordia.ca.

Description:

Cyst Reduction in a Polycystic Kidney Disease Drosophila Model Using Smac Mimics.

Biomedicines. 2019 Oct 18;7(4):

Authors: Millet-Boureima C, Chingle R, Lubell WD, Gamberi C

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) is an inherited malady affecting 12.5 million people worldwide. Therapeutic options to treat PKD are limited, due in part to lack of precise knowledge of underlying pathological mechanisms. Mimics of the second mitochondria-derived activator of caspases (Smac) have exhibited activity as antineoplastic agents and reported recently to ameliorate cysts in a murine ADPKD model, possibly by differentially targeting cystic cells and sparing the surrounding tissue. A first-in-kind Drosophila PKD model has now been employed to probe further the activity of novel Smac mimics. Substantial reduction of cystic defects was observed in the Malpighian (renal) tubules of treated flies, underscoring mechanistic conservation of the cystic pathways and potential for efficient testing of drug prototypes in this PKD model. Moreover, the observed differential rescue of the anterior and posterior tubules overall, and within their physiologically diverse intermediate and terminal regions implied a nuanced response in distinct tubular regions contingent upon the structure of the Smac mimic. Knowledge gained from studying Smac mimics reveals the capacity for the Drosophila model to precisely probe PKD pharmacology highlighting the value for such critical evaluation of factors implicated in renal function and pathology.

PMID: 31635379 [PubMed]