FFC#11/2016

Myriocin potential as a phenotype-modifyingt therapeutical in cystic fibrosis

AREA 1 Therapies to correct the underlying defect

FFC#11/2016

Myriocin potential as a phenotype-modifyingt therapeutical in cystic fibrosis
€ 0 still needed
0%
€ 70.000 goal

pRINCIPAL INVESTIGATOR

Paola Signorelli (Dipartimento di Scienze della Salute, Ospedale San Paolo, Università di Milano)

Researchers

10

Category

AREA 1 Therapies to correct the underlying defect

Duration

2 years

Goal

€ 70.000

Funds raised

€ 70.000

Objectives

Myriocin is a fungal metabolite used in traditional Chinese medicine whose efficacy in modulating cell oxidative stress was demonstrated. Researchers of this project demonstrated that myriocin significantly reduces inflammation and improves response against bacterial and fungal infections in experimental models of cystic fibrosis. Since a therapy based on the anti-oxidant effect of cysteamine in CF was recently approached, now they aim to define the mechanism by which myriocin works and to explore if myriocin it can cooperate with other drugs such as cysteamine and lumacaftor in rescuing CFTR function.

WHO ADOPTED THE PROJECT

Gruppo di Sostegno FFC di Vercelli

€ 16.000

Gruppo di Sostegno FFC di Genova “Mamme per la ricerca”

€ 30.000

Delegazione FFC Valle Scrivia Alessandria

€ 8.000

Delegazione FFC di Olbia

€ 16.000

Gruppo di Sostegno FFC di Genova “Mamme per la ricerca”

€ 30.000

Delegazione FFC Valle Scrivia Alessandria

€ 8.000

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FFC#2/2025

Developing RNA-targeted therapies to regulate gene expression and restore CFTR synthesis