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Aleksic_Supplementary Data from Nuclear IGF1R Interacts with Regulatory Regions of Chromatin to Promote RNA Polymerase II Recruitment and Gene Expression Associated with Advanced Tumor Stage

Tamara Aleksic, Nicki Gray,Xiaoning Wu, Guillaume Rieunier, Eliot Osher, Jack Mills, Clare Verrill,Richard J. Bryant, Cheng Han,Kathryn Hutchinson, Adam G. Lambert,Rajeev Kumar,Freddie C. Hamdy,Ulrike Weyer-Czernilofsky, Michael P. Sanderson, Thomas Bogenrieder, Stephen Taylor,Valentine M. Macaulay

openalex(2023)

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摘要
Supplementary file containing: Supplementary methods Table S1: Primers, probes and siRNAs used in this study. Table S2: Demographics of men treated by radical prostatectomy for prostate cancer. Table S3: IGF-1R scores and clinical parameters in men undergoing radical prostatectomy for localized prostate cancer. Table S4: ChIP-seq: mapped reads. Figure S1: Characterization of IGF-1R expression and subcellular localization in prostate cancer. Figure S2: IGF-1R ChIP-seq in human cancer cells containing nuclear IGF-1R. Figure S3: ChIP-seq identifies IGF-1R binding peaks in promoters of JUN and FAM21 but not CCDN1 or IGF1R. Figure S4: Investigating functional consequences of coincidence of IGF-1R and RNAPol2 recruitment to JUN and FAM21A promoters. Figure S5: Depletion of JUN or FAM21A delays migration towards IGF-1 but has no effect on short-term proliferation. Figure S6: JUN expression does not correlate with total IGF-1R in prostate cancer.
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Prostate Cancer
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