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Defining splicing factor requirements for androgen receptor variant synthesis in advanced prostate cancer. Defining splicing factor requirements for androgen receptor variant synthesis in advanced prostate cancer

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NIAID Data Ecosystem2026-05-01 收录
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA1044137
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To understand the function of splcing factor MFAP1 in the transcriptional regulation of anrogen receptor variants, we used the CWR22Rv1 prostate cancer cell line depleted of MFAP1 (siMFAP1) or AR-V7 (siCE3) for 72 hours. We then performed gene expression profiling analysis using data obtained from RNA-seq. Overall design: To investigate the AR-dependent and -independent global transcriptomic impact of MFAP1-depletion using CWR22Rv1 cells depleted of MFAP1 or AR-V7 using siRNA. We then performed gene expression profiling from the RNA sequencing data in response to MFAP1 or AR-V7 depletion compared to the non-targeting scrambled control.
创建时间:
2023-11-22
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