TY - JOUR
T1 - Role of ursolic acid in preventing gastrointestinal cancer
T2 - recent trends and future perspectives
AU - Chauhan, Abhishek
AU - Pathak, Vinay Mohan
AU - Yadav, Monika
AU - Chauhan, Ritu
AU - Babu, Neelesh
AU - Chowdhary, Manish
AU - Ranjan, Anuj
AU - Mathkor, Darin Mansor
AU - Haque, Shafiul
AU - Tuli, Hardeep Singh
AU - Ramniwas, Seema
AU - Yadav, Vikas
N1 - Publisher Copyright:
Copyright © 2024 Chauhan, Pathak, Yadav, Chauhan, Babu, Chowdhary, Ranjan, Mathkor, Haque, Tuli, Ramniwas and Yadav.
PY - 2024
Y1 - 2024
N2 - Gastrointestinal malignancies are one of the major worldwide health concerns. In the present review, we have assessed the plausible therapeutic implication of Ursolic Acid (UA) against gastrointestinal cancer. By modulating several signaling pathways critical in cancer development, UA could offer anti-inflammatory, anti-proliferative, and anti-metastatic properties. However, being of low oral bioavailability and poor permeability, its clinical value is restricted. To deliver and protect the drug, liposomes and polymer micelles are two UA nanoformulations that can effectively increase medicine stability. The use of UA for treating cancers is safe and appropriate with low toxicity characteristics and a predictable pharmacokinetic profile. Although the bioavailability of UA is limited, its nanoformulations could emerge as an alternative to enhance its efficacy in treating GI cancers. Further optimization and validation in the clinical trials are necessary. The combination of molecular profiling with nanoparticle-based drug delivery technologies holds the potential for bringing UA to maximum efficacy, looking for good prospects with GI cancer treatment.
AB - Gastrointestinal malignancies are one of the major worldwide health concerns. In the present review, we have assessed the plausible therapeutic implication of Ursolic Acid (UA) against gastrointestinal cancer. By modulating several signaling pathways critical in cancer development, UA could offer anti-inflammatory, anti-proliferative, and anti-metastatic properties. However, being of low oral bioavailability and poor permeability, its clinical value is restricted. To deliver and protect the drug, liposomes and polymer micelles are two UA nanoformulations that can effectively increase medicine stability. The use of UA for treating cancers is safe and appropriate with low toxicity characteristics and a predictable pharmacokinetic profile. Although the bioavailability of UA is limited, its nanoformulations could emerge as an alternative to enhance its efficacy in treating GI cancers. Further optimization and validation in the clinical trials are necessary. The combination of molecular profiling with nanoparticle-based drug delivery technologies holds the potential for bringing UA to maximum efficacy, looking for good prospects with GI cancer treatment.
KW - anticancer therapy
KW - gastrointestinal cancer
KW - molecular profiling
KW - nanoformulations
KW - nanoparticle-based drug delivery
KW - ursolic acid
UR - https://www.scopus.com/pages/publications/85200660217
U2 - 10.3389/fphar.2024.1405497
DO - 10.3389/fphar.2024.1405497
M3 - Artículo de revisión
AN - SCOPUS:85200660217
SN - 1663-9812
VL - 15
JO - Frontiers in Pharmacology
JF - Frontiers in Pharmacology
M1 - 1405497
ER -