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AuthorPrabhu, Kirti S.
AuthorKuttikrishnan, Shilpa
AuthorMariyam, Zahwa
AuthorHabeeba, Ummu
AuthorPanicker, Anu Jayanthi
AuthorMasoodi, Tariq
AuthorJunejo, Kulsoom
AuthorUddin, Shahab
Available date2025-10-13T10:03:14Z
Publication Date2025-07-17
Publication NameNaunyn Schmiedeberg S Archives of Pharmacology
Identifierhttp://dx.doi.org/10.1007/s00210-025-04297-3
CitationPrabhu, K. S., Kuttikrishnan, S., Mariyam, Z., Habeeba, U., Panicker, A. J., Masoodi, T., ... & Uddin, S. (2025). PI3 K/AKT/mTOR pathway and its role in breast cancer stem cells. Naunyn-Schmiedeberg's Archives of Pharmacology, 1-17.‏
ISSN0028-1298
URIhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105010950302&origin=inward
URIhttp://hdl.handle.net/10576/67895
AbstractCancer stem cells (CSCs) are a small subpopulation bearing self-renewal ability, mediating tumor initiation and propagation. Several molecular pathways, including the PI3K/AKT/mTOR pathway, are known to be aberrantly activated in cancers. In CSCs, PI3K/AKT/mTOR pathway has been associated with attribution of various properties to cancer cells including stemness characteristics, proliferation, migration, epithelial to mesenchymal transition, and autophagy. Thus, targeting PI3K/AKT/mTOR pathway with novel inhibitors might help to control the growth and proliferation of the breast CSC population. Though many studies have focused on PI3K/AKT/mTOR pathway in breast cancer, limited literature is available on the role of PI3K/AKT/mTOR pathway in breast CSCs. Here, in our present review, we have highlighted the role of the PI3K/AKT/mTOR signaling pathway in breast CSCs and its applications in therapeutic targeting.
SponsorThis work was supported by Medical Research Centre, HMC, Doha, Qatar (IRGC-05-SI-18–307). The authors acknowledge Qatar National Library for the open access fund support.
Languageen
PublisherSpringer
SubjectBreast cancer
Cancer stem cells
Epithelial–mesenchymal transition
PI3/AKT/mTOR
TitlePI3 K/AKT/mTOR pathway and its role in breast cancer stem cells
TypeArticle
Pagination1-17
dc.accessType Full Text


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