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Inhibitors of the mTOR signaling pathway can play an important role in breast cancer immunopathogenesis.

Authors :
Al‐Hawary, Sulieman I. Shelash
Altalbawy, Farag M. A.
Jasim, Saade Abdalkareem
Jyothi S, Renuka
Jamal, Azfar
Naiyer, Mohammed M.
Mahajan, Shriya
Kalra, Hitesh
Jawad, Mohammed Abed
Zwamel, Ahmed Hussein
Source :
Cell Biology International. Nov2024, Vol. 48 Issue 11, p1601-1611. 11p.
Publication Year :
2024

Abstract

This study explores the critical role of inhibitors targeting the mammalian target of rapamycin (mTOR) signaling pathway in breast cancer research and treatment. The mTOR pathway, a central regulator of cellular processes, has been identified as a crucial factor in the development and progression of breast cancer. The essay explains the complex molecular mechanisms through which mTOR inhibitors, such as rapamycin and its analogs, exert their anticancer effects. These inhibitors can stop cell growth, proliferation, and survival in breast cancer cells by blocking critical signaling pathways within the mTOR pathway. Furthermore, the essay discusses the implications of using mTOR inhibitors as a comprehensive therapeutic strategy. It emphasizes the potential benefits of combining mTOR inhibitors with other treatment approaches to enhance the effectiveness of breast cancer treatment. The evolving landscape of breast cancer research underscores the significance of mTOR as a therapeutic target and highlights ongoing efforts to improve and optimize mTOR inhibitors for clinical use. In conclusion, the essay asserts that inhibitors of the mTOR signaling pathway offer a promising approach in the fight against breast cancer. These inhibitors provide a focused and effective intervention targeting specific dysregulations within the mTOR pathway. As research advances, the integration of mTOR inhibitors into customized combination therapies holds excellent potential for shaping a more effective and personalized approach to breast cancer treatment, ultimately leading to improved outcomes for individuals affected by this complex and diverse disease. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10656995
Volume :
48
Issue :
11
Database :
Academic Search Index
Journal :
Cell Biology International
Publication Type :
Academic Journal
Accession number :
180279288
Full Text :
https://doi.org/10.1002/cbin.12231