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The potential molecular pathways of Astragaloside-IV in colorectal cancer: A systematic review.
- Source :
-
Biomedicine & Pharmacotherapy . Nov2023, Vol. 167, pN.PAG-N.PAG. 1p. - Publication Year :
- 2023
-
Abstract
- Astragaloside IV (AS-IV), a traditional Chinese medicine, is often used to treat cancer. Colorectal cancer imposes a heavy burden on patients and society. It is essential to update the clinical evidence supporting AS-IV in the treatment of colorectal cancer. The purpose of this review is to systematically evaluate the molecular pathway and safety of AS-IV in colorectal cancer. 7 databases were queried for Jan 2012-Dec 2022. A total of 37 related articles were retrieved. 8 papers were included to evaluate the role of AS-IV in colorectal cancer and make a review. AS-IV plays vital roles in colorectal cancer, especially in the suppression of proliferation, inducing tumor cell apoptosis, increasing immune function and reducing drug resistance. Furthermore, AS-IV has been proved to regulate many signaling pathways, which are usually affected by most cancers. However, a large-scale and well-designed multicenter randomized controlled study ensures that the safety and optimal dose of AS-IV will be determined in the future. [Display omitted] • This manuscript is the first systematic review to study the potential molecular pathways of astragaloside-IV in colorectal cancer. • The signal path figure found in the existing research for nearly 10 years was drawn in the manuscript. • AS-IV could be considered a Chinese traditional medicine with anti-colorectal cancer. • The safe and effective doses of AS-IV should be determined through large sample clinical studies in the future. [ABSTRACT FROM AUTHOR]
- Subjects :
- *COLORECTAL cancer
*IMMUNOSUPPRESSION
*CHINESE medicine
*DRUG resistance
Subjects
Details
- Language :
- English
- ISSN :
- 07533322
- Volume :
- 167
- Database :
- Academic Search Index
- Journal :
- Biomedicine & Pharmacotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 172976602
- Full Text :
- https://doi.org/10.1016/j.biopha.2023.115625