The present study aimed to investigate the roles of in the biological processes of bladder cancer cells (BCCs) . Short hairpin (sh)RNA targeting was designed and constructed, and the T24 and 5637 BCCs were selected for transfection. The cells were classified into two groups: shRNA negative control (NC) and Notch1 shRNA. MTT and Transwell assays, and flow cytometry were performed to examine the changes in cell proliferation, invasiveness, and apoptosis, respectively. In addition, reverse transcription-quantitative PCR and western blot analysis was used to detect the mRNA and protein expression levels of apoptosis-related proteins (Bax, Bid and Bcl2) and epithelial-mesenchymal transition factors (vimentin and E- and N-cadherin). Compared with that in the shRNA NC group, the Notch1 shRNA group showed significantly decreased cell proliferation rate and invasiveness; increased apoptotic rate; elevated mRNA expression levels of Bad, Bid and E-cadherin; and reduced mRNA expression levels of Bcl2, N-cadherin and vimentin. The trends for protein expression levels were the same as those for mRNA levels. silencing inhibited invasion and promoted apoptosis of BCCs.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905604 | PMC |
| http://dx.doi.org/10.3892/ol.2021.12566 | DOI Listing |
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