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DOI 10.1186/s13023-025-03740-1

Медицинская библиотека · Orphanet journal of rare diseases · 2025

mTOR pathway diseases: challenges and opportunities from bench to bedside and the mTOR node.

Mantoan Ritter Laura, Annear Nicholas M P, Baple Emma L, Ben-Chaabane Leila Y, Bodi Istvan, Brosson Lauren, Cadwgan Jill E, Coslett Bryn, Crosby Andrew H, Davies D Mark, Daykin Nicola, Dedeurwaerdere Stefanie, Dühring Fenger Christina, Dunlop Elaine A, Elmslie Frances V, Girodengo Marie, Hambleton Sophie, Jansen Anna C, Johnson Simon R, Kearley Kelly C, Kingswood John C, Laaniste Liisi, Lachlan Katherine, Latchford Andrew, Madsen Ralitsa R, Mansour Sahar, Mihaylov Simeon R, Muhammed Louwai, Oliver Claire, Pepper Tom, Rawlins Lettie E, Schim van der Loeff Ina, Siddiqui Ata, Takhar Pooja, Tatton-Brown Katrina, Tee Andrew R, Tibarewal Priyanka, Tye Charlotte, Ultanir Sila K, Vanhaesebroeck Bart, Zare Benjamin, Pal Deb K, Bateman Joseph M

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Аннотация

Mechanistic target of rapamycin (mTOR) is a highly conserved serine/threonine kinase that regulates key cellular processes including cell growth, autophagy and metabolism. Hyperactivation of the mTOR pathway causes a group of rare and ultrarare genetic diseases. mTOR pathway diseases have diverse clinical manifestations that are managed by distinct medical disciplines but share a common underlying molecular basis. There is a now a deep understanding of the molecular underpinning that regulates the mTOR pathway but effective treatments for most mTOR pathway diseases are lacking. Translating scientific knowledge into clinical applications to benefit the unmet clinical needs of patients is a major challenge common to many rare diseases. In this article we expound how mTOR pathway diseases provide an opportunity to coordinate basic and translational disease research across the group, together with industry, medical research foundations, charities and patient groups, by pooling expertise and driving progress to benefit patients. We outline the germline and somatic mutations in the mTOR pathway that cause rare diseases and summarise the prevalence, genetic basis, clinical manifestations, pathophysiology and current treatments for each disease in this group. We describe the challenges and opportunities for progress in elucidating the underlying mechanisms, improving diagnosis and prognosis, as well as the development and approval of new therapies for mTOR pathway diseases. We illustrate the crucial role of patient public involvement and engagement in rare disease and mTOR pathway disease research. Finally, we explain how the mTOR Pathway Diseases node, part of the Research Disease Research UK Platform, will address these challenges to improve the understanding, diagnosis and treatment of mTOR pathway diseases.

Для цитирования: Mantoan Ritter Laura, Annear Nicholas M P, Baple Emma L, Ben-Chaabane Leila Y, Bodi Istvan, Brosson Lauren, Cadwgan Jill E, Coslett Bryn, Crosby Andrew H, Davies D Mark, Daykin Nicola, Dedeurwaerdere Stefanie, Dühring Fenger Christina, Dunlop Elaine A, Elmslie Frances V, Girodengo Marie, Hambleton Sophie, Jansen Anna C, Johnson Simon R, Kearley Kelly C, Kingswood John C, Laaniste Liisi, Lachlan Katherine, Latchford Andrew, Madsen Ralitsa R, Mansour Sahar, Mihaylov Simeon R, Muhammed Louwai, Oliver Claire, Pepper Tom, Rawlins Lettie E, Schim van der Loeff Ina, Siddiqui Ata, Takhar Pooja, Tatton-Brown Katrina, Tee Andrew R, Tibarewal Priyanka, Tye Charlotte, Ultanir Sila K, Vanhaesebroeck Bart, Zare Benjamin, Pal Deb K, Bateman Joseph M. mTOR pathway diseases: challenges and opportunities from bench to bedside and the mTOR node.. Orphanet journal of rare diseases. 2025. DOI: 10.1186/s13023-025-03740-1.

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