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Nanotherapeutics targeting autophagy regulation for improved cancer therapy.

Authors :
Liu Y
Wang Y
Zhang J
Peng Q
Wang X
Xiao X
Shi K
Source :
Acta pharmaceutica Sinica. B [Acta Pharm Sin B] 2024 Jun; Vol. 14 (6), pp. 2447-2474. Date of Electronic Publication: 2024 Mar 18.
Publication Year :
2024

Abstract

The clinical efficacy of current cancer therapies falls short, and there is a pressing demand to integrate new targets with conventional therapies. Autophagy, a highly conserved self-degradation process, has received considerable attention as an emerging therapeutic target for cancer. With the rapid development of nanomedicine, nanomaterials have been widely utilized in cancer therapy due to their unrivaled delivery performance. Hence, considering the potential benefits of integrating autophagy and nanotechnology in cancer therapy, we outline the latest advances in autophagy-based nanotherapeutics. Based on a brief background related to autophagy and nanotherapeutics and their impact on tumor progression, the feasibility of autophagy-based nanotherapeutics for cancer treatment is demonstrated. Further, emerging nanotherapeutics developed to modulate autophagy are reviewed from the perspective of cell signaling pathways, including modulation of the mammalian target of rapamycin (mTOR) pathway, autophagy-related (ATG) and its complex expression, reactive oxygen species (ROS) and mitophagy, interference with autophagosome-lysosome fusion, and inhibition of hypoxia-mediated autophagy. In addition, combination therapies in which nano-autophagy modulation is combined with chemotherapy, phototherapy, and immunotherapy are also described. Finally, the prospects and challenges of autophagy-based nanotherapeutics for efficient cancer treatment are envisioned.<br /> (© 2024 The Authors.)

Details

Language :
English
ISSN :
2211-3835
Volume :
14
Issue :
6
Database :
MEDLINE
Journal :
Acta pharmaceutica Sinica. B
Publication Type :
Academic Journal
Accession number :
38828133
Full Text :
https://doi.org/10.1016/j.apsb.2024.03.019