The mTOR Signaling Pathway and mTOR Inhibitors in Cancer: Next-Generation Inhibitors and Approaches

dc.contributor.author Ihlamur, Murat
dc.contributor.author Akgul, Busra
dc.contributor.author Zengin, Yagmur
dc.contributor.author Korkut, Senay Vural
dc.contributor.author Kelleci, Kubra
dc.contributor.author Abamor, Emrah Sefik
dc.date.accessioned 2026-01-30T14:54:53Z
dc.date.available 2026-01-30T14:54:53Z
dc.date.issued 2024
dc.description Zengin, Yağmur/0000-0003-4534-706X; Ihlamur, Murat/0000-0002-0458-5638; en_US
dc.description.abstract mTOR is a serine/threonine kinase that plays various roles in cell growth, proliferation, and metabolism. mTOR signaling in cancer becomes irregular. Therefore, drugs targeting mTOR have been developed. Although mTOR inhibitors rapamycin and rapamycin rapalogs (everolimus, rapamycin, temsirolimus, deforolimus, etc.) and new generation mTOR inhibitors (Rapalink, Dual PI3K/mTOR inhibitors, etc.) are used in cancer treatments, mTOR resistance mechanisms may inhibit the efficacy of these drugs. Therefore, new inhibition approaches are developed. Although these new inhibition approaches have not been widely investigated in cancer treatment, the use of nanoparticles has been evaluated as a new treatment option in a few types of cancer.This review outlines the functions of mTOR in the cancer process, its resistance mechanisms, and the efficiency of mTOR inhibitors in cancer treatment. Furthermore, it discusses the next-generation mTOR inhibitors and inhibition strategies created using nanoparticles.Since mTOR resistance mechanisms prevent the effects of mTOR inhibitors used in cancer treatments, new inhibition strategies should be developed. Inhibition approaches are created using nanoparticles, and one of them offers a promising treatment option with evidence supporting its effectiveness. en_US
dc.identifier.doi 10.2174/1566524023666230509161645
dc.identifier.issn 1566-5240
dc.identifier.issn 1566-5240
dc.identifier.issn 1875-5666
dc.identifier.scopus 2-s2.0-85174078849
dc.identifier.uri https://doi.org/10.2174/1566524023666230509161645
dc.identifier.uri https://acikerisim2.beykoz.edu.tr/handle/123456789/203
dc.language.iso en en_US
dc.publisher Bentham Science Publishing Ltd en_US
dc.relation.ispartof Current Molecular Medicine en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject MTOR en_US
dc.subject MTOR Inhibitor en_US
dc.subject Cancer en_US
dc.subject Resistance Mechanisms en_US
dc.subject Nanoparticles en_US
dc.subject Next-Generation Inhibitors en_US
dc.subject Approaches en_US
dc.title The mTOR Signaling Pathway and mTOR Inhibitors in Cancer: Next-Generation Inhibitors and Approaches en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Zengin, Yağmur/0000-0003-4534-706X
gdc.author.id Ihlamur, Murat/0000-0002-0458-5638
gdc.author.scopusid 57402670600
gdc.author.scopusid 57983283400
gdc.author.scopusid 58885262500
gdc.author.scopusid 34877263200
gdc.author.scopusid 57860203000
gdc.author.scopusid 54408016800
gdc.author.wosid Korkut, Senay/Aba-2454-2020
gdc.author.wosid Akgül, Buşra/Jep-2725-2023
gdc.author.wosid Ihlamur, Murat/Gwz-9070-2022
gdc.author.wosid Kelleci, Kubra/Gxn-1324-2022
gdc.description.department Beykoz University en_US
gdc.description.departmenttemp [Ihlamur, Murat; Akgul, Busra; Kelleci, Kubra; Abamor, Emrah Sefik] Yildiz Tech Univ, Fac Chem & Met Engn, Dept Bioengn, Istanbul, Turkiye; [Ihlamur, Murat] Biruni Univ, Dept Elect & Automat, Istanbul, Turkiye; [Zengin, Yagmur] Bogazici Univ, Biomed Engn Inst, Dept Biomed Engn, Istanbul, Turkiye; [Korkut, Senay Vural] Yildiz Tech Univ, Fac Arts & Sci, Dept Mol Biol & Genet, Istanbul, Turkiye; [Kelleci, Kubra] Beykoz Univ, Dept Med Serv & Tech, Istanbul, Turkiye en_US
gdc.description.endpage 494 en_US
gdc.description.issue 4 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 478 en_US
gdc.description.volume 24 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q3
gdc.identifier.pmid 37165594
gdc.identifier.wos WOS:001202976600001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

Files