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NO- and H2S- releasing nanomaterials: A crosstalk signaling pathway in cancer.
- Source :
-
Nitric Oxide . Oct2024, Vol. 151, p17-30. 14p. - Publication Year :
- 2024
-
Abstract
- The gasotransmitters nitric oxide (NO) and hydrogen sulfide (H 2 S) play important roles not only in maintaining physiological functions, but also in pathological conditions and events. Importantly, these molecules show a complex interplay in cancer biology, demonstrating both tumor-promoting and anti-tumor activities depending on their concentration, flux, and the environmental redox state. Additionally, various cell types respond differently to NO and H 2 S. These gasotransmitters can be synergistically combined with traditional anticancer treatments such as radiotherapy, immunotherapy, chemotherapy, and phototherapy. Notably, NO, and more recently H 2 S, have been shown to reverse multidrug resistance. Nanomaterials to deliver NO donors and, to a lesser extent, H 2 S donors, have emerged as a promising approach for targeted delivery of these gasotransmitters. Nanotechnology has advanced the delivery of anticancer drugs, enhancing efficiency and reducing side effects on non-cancerous cells. This review highlights recent progress in the design of NO and H 2 S-releasing nanomaterials for anticancer effects. It also explores the interactions between NO and H 2 S, which are crucial for developing combined therapies and nanomedicines with minimal side effects. • This review integrates recent nitric oxide (NO) and hydrogen sulfide (H 2 S) releasing nanomaterials in cancer treatment. • Research gaps are identified where further contributions can enhance understanding of the physiological roles of NO and H 2 S. • Gaps are explored throughout, highlighting potential avenues for exploration in cancer treatment using NO and H 2 S. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 10898603
- Volume :
- 151
- Database :
- Academic Search Index
- Journal :
- Nitric Oxide
- Publication Type :
- Academic Journal
- Accession number :
- 179503752
- Full Text :
- https://doi.org/10.1016/j.niox.2024.08.002