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Pien Tze Huang induces apoptosis and inhibits proliferation of 5-fluorouracil-resistant colorectal carcinoma cells via increasing miR-22 expression.

Authors :
ZHAORONG CHEN
ALING SHEN
LIYA LIU
YOUQIN CHEN
JIANFENG CHU
QIAOYAN CAI
FEI QI
SFERRA, THOMAS JOSEPH
JUN PENG
Source :
Experimental & Therapeutic Medicine. Oct2017, Vol. 14 Issue 4, p3533-3540. 8p.
Publication Year :
2017

Abstract

The well-known traditional Chinese medicine formula Pien Tze Huang (PZH) has long been used to treat various malignancies, including colorectal cancer (CRC). It was recently reported that PZH possesses the ability to overcome multidrug resistance in CRC cells. In the present study, a 5-fluorouracil (5-FU) resistant human CRC cell line (HCT-8/5-FU) was used to further evaluate the effect of PZH on chemotherapy (chemo)-resistance and investigate the mechanisms through which this occurs. The results identified that PZH significantly reduced the viability and cell density of HCT-8/5-FU cells in a dose- and time-dependent manner (P<0.05). PZH inhibited cell survival, reduced the proportion of cells in S-phase, and suppressed the expression of pro-proliferative proteins cyclin D1 and cyclin-dependent kinase 4. In addition, PZH treatment induced nuclear condensation and fragmentation, activated caspase-9 and -3 and increased the pro-apoptotic Bcl-2-associated X protein/B-cell lymphoma 2 protein ratio. Furthermore, PZH treatment upregulated the expression of microRNA-22 (miR-22) and downregulated the expression of c-Myc (a target gene of miR-22). In conclusion, the findings from the present study suggest that PZH can overcome chemo-resistance in cancer cells, likely through increasing miR-22 expression, and by reversing the imbalance between levels of proliferation and apoptosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17920981
Volume :
14
Issue :
4
Database :
Academic Search Index
Journal :
Experimental & Therapeutic Medicine
Publication Type :
Academic Journal
Accession number :
125048854
Full Text :
https://doi.org/10.3892/etm.2017.4951