Data of relative mRNA and protein abundances of androgen receptor splice variants in castration-resistant prostate cancer
These data include secondary analysis of publicly available RNA-seq data from castration-resistant prostate cancer (CRPC) patients as well as RT-qPCR and Western blotting analyses of patient-derived xenograft models and a CRPC cell line. We applied Spearman correlation analysis to assess the relatio...
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doaj-5ee0fdff56c3482a99721247b5a2885d2021-01-24T04:28:05ZengElsevierData in Brief2352-34092021-02-0134106774Data of relative mRNA and protein abundances of androgen receptor splice variants in castration-resistant prostate cancerTianfang Ma0Nathan Ungerleider1Derek Y. Zhang2Eva Corey3Erik K. Flemington4Yan Dong5Department of Structural and Cellular Biology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA, USADepartment of Pathology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA, USALusher Charter School, New Orleans, LA 70115, USADepartment of Urology, University of Washington, Seattle, WA, USADepartment of Pathology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA, USA; Corresponding authors.Department of Structural and Cellular Biology, Tulane University School of Medicine, Tulane Cancer Center, New Orleans, LA, USA; Corresponding authors.These data include secondary analysis of publicly available RNA-seq data from castration-resistant prostate cancer (CRPC) patients as well as RT-qPCR and Western blotting analyses of patient-derived xenograft models and a CRPC cell line. We applied Spearman correlation analysis to assess the relationship between canonical androgen receptor (AR) splicing and alternative AR splicing. We also assessed the ratio of AR splice variants (AR-Vs) to the full-length AR (AR-FL) at the RNA and protein levels by absolute RT-qPCR and Western blotting, respectively. These data are critical for studying the mechanisms underlying upregulated expression of AR-Vs after AR-directed therapies and the importance of AR-Vs to castration-resistant progression of prostate cancer. Data presented here are related to the research article by Ma et al., “Increased transcription and high translation efficiency lead to accumulation of androgen receptor splice variant after androgen deprivation therapy”, Cancer Lett. In Press [1].http://www.sciencedirect.com/science/article/pii/S2352340921000585Androgen receptorSplice variantsCastration-resistant prostate cancerAndrogen deprivation therapy |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tianfang Ma Nathan Ungerleider Derek Y. Zhang Eva Corey Erik K. Flemington Yan Dong |
spellingShingle |
Tianfang Ma Nathan Ungerleider Derek Y. Zhang Eva Corey Erik K. Flemington Yan Dong Data of relative mRNA and protein abundances of androgen receptor splice variants in castration-resistant prostate cancer Data in Brief Androgen receptor Splice variants Castration-resistant prostate cancer Androgen deprivation therapy |
author_facet |
Tianfang Ma Nathan Ungerleider Derek Y. Zhang Eva Corey Erik K. Flemington Yan Dong |
author_sort |
Tianfang Ma |
title |
Data of relative mRNA and protein abundances of androgen receptor splice variants in castration-resistant prostate cancer |
title_short |
Data of relative mRNA and protein abundances of androgen receptor splice variants in castration-resistant prostate cancer |
title_full |
Data of relative mRNA and protein abundances of androgen receptor splice variants in castration-resistant prostate cancer |
title_fullStr |
Data of relative mRNA and protein abundances of androgen receptor splice variants in castration-resistant prostate cancer |
title_full_unstemmed |
Data of relative mRNA and protein abundances of androgen receptor splice variants in castration-resistant prostate cancer |
title_sort |
data of relative mrna and protein abundances of androgen receptor splice variants in castration-resistant prostate cancer |
publisher |
Elsevier |
series |
Data in Brief |
issn |
2352-3409 |
publishDate |
2021-02-01 |
description |
These data include secondary analysis of publicly available RNA-seq data from castration-resistant prostate cancer (CRPC) patients as well as RT-qPCR and Western blotting analyses of patient-derived xenograft models and a CRPC cell line. We applied Spearman correlation analysis to assess the relationship between canonical androgen receptor (AR) splicing and alternative AR splicing. We also assessed the ratio of AR splice variants (AR-Vs) to the full-length AR (AR-FL) at the RNA and protein levels by absolute RT-qPCR and Western blotting, respectively. These data are critical for studying the mechanisms underlying upregulated expression of AR-Vs after AR-directed therapies and the importance of AR-Vs to castration-resistant progression of prostate cancer. Data presented here are related to the research article by Ma et al., “Increased transcription and high translation efficiency lead to accumulation of androgen receptor splice variant after androgen deprivation therapy”, Cancer Lett. In Press [1]. |
topic |
Androgen receptor Splice variants Castration-resistant prostate cancer Androgen deprivation therapy |
url |
http://www.sciencedirect.com/science/article/pii/S2352340921000585 |
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