TY - JOUR
T1 - ALSUntangled #80
T2 - ISRIB (Integrated stress response InhiBitor)
AU - Mascias Cadavid, Javier
AU - Mena Bravo, Anna
AU - Barkhaus, Paul
AU - Barnes, Benjamin
AU - Benatar, Michael
AU - Breevoort, Sarah
AU - Brown, Andrew
AU - Carter, Gregory T.
AU - Crayle, Jesse
AU - Foucher, Juliette
AU - Heiman-Patterson, Terry
AU - Hobson, Esther
AU - Jackson, Carlayne
AU - Jhooty, Sartaj
AU - Mallon, Elise
AU - Mcdermott, Christopher
AU - Pattee, Gary
AU - Pierce, Kaitlyn
AU - Pioro, Erik
AU - Ratner, Dylan
AU - Rivner, Michael
AU - Tito, Elia
AU - Wicks, Paul
AU - Bedlack, Richard
N1 - Publisher Copyright:
© 2025 World Federation of Neurology on behalf of the Research Group on Motor Neuron Diseases.
PY - 2025
Y1 - 2025
N2 - ALSUntangled reviews alternative and off-label treatments for people living with amyotrophic lateral sclerosis (PALS). Here we assess ISRIB, a molecule that attenuates the integrated stress response (ISR). The ISR is an intracellular signaling network through which cells normally respond to stress, but in ALS it appears to be overactive, leading to the formation of “stress granules” which some but not all investigators believe can triggerapoptotic cell death. ISRIB can attenuate the formation of these stress granules while still allowing parts of protein synthesis to continue. Pre-clinical data demonstrate that ISRIB is beneficial in cell models of ALS. A small number of patients taking ISRIB in Spain report symptomatic improvements with little or no side effects, though we have not been able to independently verify these benefits. There are no clinical trials evaluating ISRIB in any condition and questions about its solubility and bioavailability have arisen. Currently, we do not have enough evidence to endorse the use of ISRIB for treating ALS. We support further research in disease models and clinical trials to study pharmacokinetics, safety and efficacy.
AB - ALSUntangled reviews alternative and off-label treatments for people living with amyotrophic lateral sclerosis (PALS). Here we assess ISRIB, a molecule that attenuates the integrated stress response (ISR). The ISR is an intracellular signaling network through which cells normally respond to stress, but in ALS it appears to be overactive, leading to the formation of “stress granules” which some but not all investigators believe can triggerapoptotic cell death. ISRIB can attenuate the formation of these stress granules while still allowing parts of protein synthesis to continue. Pre-clinical data demonstrate that ISRIB is beneficial in cell models of ALS. A small number of patients taking ISRIB in Spain report symptomatic improvements with little or no side effects, though we have not been able to independently verify these benefits. There are no clinical trials evaluating ISRIB in any condition and questions about its solubility and bioavailability have arisen. Currently, we do not have enough evidence to endorse the use of ISRIB for treating ALS. We support further research in disease models and clinical trials to study pharmacokinetics, safety and efficacy.
KW - ISR
KW - ISRIB
KW - stress granules
UR - https://www.scopus.com/pages/publications/105012612403
UR - https://www.scopus.com/pages/publications/105012612403#tab=citedBy
U2 - 10.1080/21678421.2025.2542919
DO - 10.1080/21678421.2025.2542919
M3 - Article
C2 - 40762148
AN - SCOPUS:105012612403
SN - 2167-8421
VL - 26
SP - 821
EP - 824
JO - Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
JF - Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
IS - 7-8
ER -