Inhibition of stearoyl CoA desaturase-1 activity suppresses tumour progression and improves prognosis in human bladder cancer.
Chiyuan PiaoXiaolu CuiBo ZhanJun LiZeliang LiZhenhua LiXiankui LiuJianbin BiZhe ZhangChui-Ze KongPublished in: Journal of cellular and molecular medicine (2018)
Urinary bladder neoplasm is one of the most common cancers worldwide. Cancer stem cells (CSCs) have been proven to be an important cause of cancer progression and poor prognosis. In the present study, we established bladder CSCs and identified the crucial differentially expressed genes (DEGs) between these cells and parental bladder cancer cells. Analyses of bioinformatics data and clinical samples from local hospitals showed that stearoyl CoA desaturase-1 (SCD) was the key factor among the DEGs. A significant correlation between SCD gene expression and poor prognosis among patients with bladder cancer was observed in our data. Loss-of-function experiments further revealed that the SCD inhibitor A939572 and SCD gene interference reduced cell proliferation and invasion. The above data suggest that SCD may serve as a novel marker for the prediction of tumour progression and poor prognosis in patients with bladder cancer.
Keyphrases
- poor prognosis
- cancer stem cells
- long non coding rna
- gene expression
- electronic health record
- spinal cord injury
- big data
- induced apoptosis
- genome wide
- endothelial cells
- dna methylation
- signaling pathway
- fatty acid
- papillary thyroid
- cell cycle arrest
- cell proliferation
- artificial intelligence
- data analysis
- deep learning
- childhood cancer
- endoplasmic reticulum stress
- pi k akt
- muscle invasive bladder cancer