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Beta-elemene increases chemosensitivity to 5-fluorouracil through down-regulating microRNA-191 expression in colorectal carcinoma cells.
- Source :
-
Journal of cellular biochemistry [J Cell Biochem] 2018 Aug; Vol. 119 (8), pp. 7032-7039. Date of Electronic Publication: 2018 May 08. - Publication Year :
- 2018
-
Abstract
- Colorectal carcinoma is a common malignant tumor occurring in the alimentary system. Despite developments of modern medicine, developed resistance to 5-fluorouracil (5-FU) may lead to poor prognosis. Herein, we aimed to explore the effects of beta-elemene on colorectal carcinoma cells (HCT116 and HT29) as well as the underlying mechanisms. Beta-elemene reduced cell viability and induced apoptosis in HCT116 and HT29 cells. Increased apoptosis following beta-elemene exposure was due to enhanced sensitivity to 5-FU through down-regulating miR-191. Expression of key kinases, including Wnt3a, and β-catenin, were down-regulated by beta-elemene through a miR-191 mechanism. Moreover, beta-elemene might improve resistance of colorectal carcinoma cells to 5-FU by down-regulating miR-191, thereby inhibiting the Wnt/β-catenin pathway.<br /> (© 2018 Wiley Periodicals, Inc.)
- Subjects :
- Colorectal Neoplasms genetics
Colorectal Neoplasms metabolism
Colorectal Neoplasms pathology
Fluorouracil agonists
HCT116 Cells
Humans
MicroRNAs genetics
Neoplasm Proteins biosynthesis
Neoplasm Proteins genetics
RNA, Neoplasm genetics
Sesquiterpenes agonists
Wnt Signaling Pathway drug effects
Wnt3A Protein biosynthesis
Wnt3A Protein genetics
beta Catenin biosynthesis
beta Catenin genetics
Colorectal Neoplasms drug therapy
Down-Regulation drug effects
Fluorouracil pharmacology
Gene Expression Regulation, Neoplastic drug effects
MicroRNAs biosynthesis
RNA, Neoplasm biosynthesis
Sesquiterpenes pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4644
- Volume :
- 119
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Journal of cellular biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 29737579
- Full Text :
- https://doi.org/10.1002/jcb.26914