: Repeat expansions in the C9orf72 gene are the most common genetic cause of (ALS) and frontotemporal dementia (FTD). Like other genetic forms of neurodegeneration, pinpointing the precise mechanism(s) by which this mutation leads to neuronal death remains elusive, and this lack of knowledge hampers the development of therapy for C9orf72-related disease. We used an agnostic approach based on genomic data (n = 41,273 ALS and healthy samples, and n = 1,516 C9orf72 carriers) to overcome these bottlenecks. Our drug-repurposing screen, based on gene- and expression-pattern matching and information about the genetic variants influencing onset age among C9orf72 carriers, identified acamprosate, a γ-aminobutyric acid analog, as a potentially repurposable treatment for patients carrying C9orf72 repeat expansions. We validated its neuroprotective effect in cell models and showed comparable efficacy to riluzole, the current standard of care. Our work highlights the potential value of genomics in repurposing drugs in situations where the underlying pathomechanisms are inherently complex. VIDEO ABSTRACT.

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data / Saez-Atienzar, Sara; Souza, Cleide dos Santos; Chia, Ruth; Beal, Selina N.; Lorenzini, Ileana; Huang, Ruili; Levy, Jennifer; Burciu, Camelia; Ding, Jinhui; Gibbs, J. Raphael; Jones, Ashley; Dewan, Ramita; Pensato, Viviana; Peverelli, Silvia; Corrado, Lucia; van Vugt, Joke J. F. A.; van Rheenen, Wouter; Tunca, Ceren; Bayraktar, Elif; Xia, Menghang; Baloh, Robert H.; Bowser, Robert; Brady, Christopher B.; Brice, Alexis; Broach, James; Camu, William; Chia, Ruth; Chio, Adriano; Cooper-Knock, John; Cusi, Daniele; Ding, Jinhui; Drepper, Carsten; Drory, Vivian E.; Dunckley, Travis L.; Feldman, Eva; Floeter, Mary Kay; Fratta, Pietro; Gerhard, Glenn; Gibbs, J. Raphael; Gibson, Summer B.; Glass, Jonathan D.; Goutman, Stephen A.; Hardy, John; Harms, Matthew B.; Heiman-Patterson, Terry D.; Jansson, Lilja; Kirby, Janine; Laaksovirta, Hannu; Landers, John E.; Landi, Francesco; Le Ber, Isabelle; Lumbroso, Serge; Guissart, Claire; Macgowan, Daniel JL.; Maragakis, Nicholas J.; Mora, Gabriele; Mouzat, Kevin; Myllykangas, Liisa; Orrell, Richard W.; Ostrow, Lyle W.; Pickering-Brown, Stuart; Pioro, Erik P.; Pulst, Stefan M.; Ravits, John M.; Renton, Alan E.; Robberecht, Wim; Rogaeva, Ekaterina; Rothstein, Jeffrey D.; Salvi, Erika; Scholz, Sonja W.; Sendtner, Michael; Shaw, Pamela J.; Sidle, Katie C.; Simmons, Zachary; Stone, David J.; Tienari, Pentti J.; Traynor, Bryan J.; Trojanowski, John Q.; Troncoso, Juan C.; Valori, Miko; Van Damme, Philip; Van Deerlin, Vivianna M.; Van Den Bosch, Ludo; Zinman, Lorne; Angelocola, Stefania M.; Ausiello, Francesco P.; Barberis, Marco; Bartolomei, Ilaria; Battistini, Stefania; Bersano, Enrica; Bisogni, Giulia; Borghero, Giuseppe; Brunetti, Maura; Cabona, Corrado; Calvo, Andrea; Canale, Fabrizio; Canosa, Antonio; Cantisani, Teresa A.; Capasso, Margherita; Caponnetto, Claudia; Cardinali, Patrizio; Carrera, Paola; Casale, Federico; Chio, Adriano; Colletti, Tiziana; Conforti, Francesca L.; Conte, Amelia; Conti, Elisa; Corbo, Massimo; Cuccu, Stefania; Bella, Eleonora Dalla; D'Errico, Eustachio; Demarco, Giovanni; Dubbioso, Raffaele; Ferrarese, Carlo; Ferraro, Pilar M.; Filippi, Massimo; Fini, Nicola; Floris, Gianluca; Fuda, Giuseppe; Gallone, Salvatore; Gianferrari, Giulia; Giannini, Fabio; Grassano, Maurizio; Greco, Lucia; Iazzolino, Barbara; Introna, Alessandro; La Bella, Vincenzo; Lattante, Serena; Lauria, Giuseppe; Liguori, Rocco; Logroscino, Giancarlo; Logullo, Francesco O.; Lunetta, Christian; Mandich, Paola; Mandrioli, Jessica; Manera, Umberto; Manganelli, Fiore; Marangi, Giuseppe; Marinou, Kalliopi; Marrosu, Maria Giovanna; Martinelli, Ilaria; Messina, Sonia; Moglia, Cristina; Monsurrò, Maria Rosaria; Mora, Gabriele; Mosca, Lorena; Murru, Maria R.; Origone, Paola; Passaniti, Carla; Petrelli, Cristina; Petrucci, Antonio; Pirisi, Angelo; Pozzi, Susanna; Pugliatti, Maura; Quattrini, Angelo; Ricci, Claudia; Riolo, Giulia; Riva, Nilo; Russo, Massimo; Sabatelli, Mario; Salamone, Paolina; Salivetto, Marco; Salvi, Fabrizio; Santarelli, Marialuisa; Sbaiz, Luca; Sideri, Riccardo; Simone, Isabella; Simonini, Cecilia; Spataro, Rossella; Tanel, Raffaella; Tedeschi, Gioacchino; Ticca, Anna; Torriello, Antonella; Tranquilli, Stefania; Tremolizzo, Lucio; Trojsi, Francesca; Vasta, Rosario; Vacchiano, Veria; Vita, Giuseppe; Volanti, Paolo; Zollino, Marcella; Zucchi, Elisabetta; Silani, Vincenzo; Fogh, Isabella; Ticozzi, Nicola; Ratti, Antonia; Tiloca, Cinzia; Peverelli, Silvia; Gellera, Cinzia; Pinter, Giuseppe Lauria; Taroni, Franco; Pensato, Viviana; Castellotti, Barbara; Comi, Giacomo P.; Corti, Stefania; Del Bo, Roberto; Cereda, Cristina; Ceroni, Mauro; Gagliardi, Stella; Corrado, Lucia; Mazzini, Letizia; Sorarù, Gianni; Raggi, Flavia; Siciliano, Gabriele; Simoncini, Costanza; Lo Gerfo, Annalisa; Filosto, Massimiliano; Inghilleri, Maurizio; Ferlini, Alessandra; Van Damme, Philip; Corcia, Philippe; Couratier, Philippe; Vourc'H, Patrick; Hardiman, Orla; Mclaughlin, Russell; Gotkine, Marc; Drory, Vivian; Ticozzi, Nicola; Silani, Vincenzo; van den Veldink, Jan H.; Berg, Leonard H.; de Carvalho, Mamede; Mora Pardina, Jesus S.; Povedano, Monica; Andersen, Peter; Weber, Markus; Başak, Ayşe Nazlı; Al-Chalabi, Ammar; Shaw, Chris; Shaw, Pamela J.; Morrison, Karen E.; Landers, John E.; Glass, Jonathan D.; Iacoangeli, Alfredo; Shatunov, Aleksey; Tiloca, Cinzia; Ticozzi, Nicola; Verde, Federico; Mazzini, Letizia; Kenna, Kevin; Al Khleifat, Ahmad; Opie-Martin, Sarah; Raggi, Flavia; Filosto, Massimiliano; Piccinelli, Stefano Cotti; Padovani, Alessandro; Gagliardi, Stella; Inghilleri, Maurizio; Ferlini, Alessandra; Vasta, Rosario; Calvo, Andrea; Moglia, Cristina; Canosa, Antonio; Manera, Umberto; Grassano, Maurizio; Mandrioli, Jessica; Mora, Gabriele; Lunetta, Christian; Tanel, Raffaella; Trojsi, Francesca; Cardinali, Patrizio; Gallone, Salvatore; Brunetti, Maura; Galimberti, Daniela; Serpente, Maria; Fenoglio, Chiara; Scarpini, Elio; Comi, Giacomo P.; Corti, Stefania; Del Bo, Roberto; Ceroni, Mauro; Pinter, Giuseppe Lauria; Taroni, Franco; Bella, Eleonora Dalla; Bersano, Enrica; Curtis, Charles J.; Lee, Sang Hyuck; Chung, Raymond; Patel, Hamel; Morrison, Karen E.; Cooper-Knock, Johnathan; Shaw, Pamela J.; Breen, Gerome; Dobson, Richard J. B.; Dalgard, Clifton L.; Adeleye, Adelani; Alba, Camille; Bacikova, Dagmar; Dalgard, Clifton L.; Hupalo, Daniel N.; McGrath Martinez, Elisa; Soltis, Anthony R.; Sukumar, Gauthaman; Viollet, Coralie; Wilkerson, Matthew D.; Scholz, Sonja W.; Al-Chalabi, Ammar; van den Berg, Leonard H.; Mclaughlin, Russell; Hardiman, Orla; Cereda, Cristina; Sorarù, Gianni; D'Alfonso, Sandra; Chandran, Siddharthan; Pal, Suvankar; Ratti, Antonia; Gellera, Cinzia; Johnson, Kory; Doucet-O'Hare, Tara; Pasternack, Nicholas; Wang, Tongguang; Nath, Avindra; Siciliano, Gabriele; Silani, Vincenzo; Başak, Ayşe Nazlı; Veldink, Jan H.; Camu, William; Glass, Jonathan D.; Landers, John E.; Chiò, Adriano; Sattler, Rita; Shaw, Christopher E.; Ferraiuolo, Laura; Fogh, Isabella; Traynor, Bryan J.. - In: CELL GENOMICS. - ISSN 2666-979X. - 4:(2024). [10.1016/j.xgen.2024.100679]

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data

Ferraro, Pilar M.;Filippi, Massimo;
2024-01-01

Abstract

: Repeat expansions in the C9orf72 gene are the most common genetic cause of (ALS) and frontotemporal dementia (FTD). Like other genetic forms of neurodegeneration, pinpointing the precise mechanism(s) by which this mutation leads to neuronal death remains elusive, and this lack of knowledge hampers the development of therapy for C9orf72-related disease. We used an agnostic approach based on genomic data (n = 41,273 ALS and healthy samples, and n = 1,516 C9orf72 carriers) to overcome these bottlenecks. Our drug-repurposing screen, based on gene- and expression-pattern matching and information about the genetic variants influencing onset age among C9orf72 carriers, identified acamprosate, a γ-aminobutyric acid analog, as a potentially repurposable treatment for patients carrying C9orf72 repeat expansions. We validated its neuroprotective effect in cell models and showed comparable efficacy to riluzole, the current standard of care. Our work highlights the potential value of genomics in repurposing drugs in situations where the underlying pathomechanisms are inherently complex. VIDEO ABSTRACT.
2024
C9orf72
acamprosate
age at onset
amyotrophic lateral sclerosis
drug repurposing
frontotemporal dementia
translation
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/172457
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