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The ETS family member GABPa mediates the development of castrate-resistant prostate cancer

ChEBI2014-05-21 更新2026-07-21 收录

前列腺癌分子机制

去势抵抗性前列腺癌

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-49093 数据链接链接失效反馈

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资源简介：

The ETS family member GABPa mediates the development of castrate-resistant prostate cancer

应用场景：

创建时间：

2014-05-21

前列腺癌分子机制

激素受体功能

Androgen receptor (AR) signaling pathway remains the foremost target of novel therapeutics for castration-resistant prostate cancer (CRPC). However, the expression of constitutively active AR variants

NIAID Data Ecosystem60

Circular RNA hsa_circ_0075542 acts as a sponge for microRNA-1197 to suppress malignant characteristics and promote apoptosis in prostate cancer cells

前列腺癌分子机制

环状RNA功能研究

Numerous differentially expressed circular RNAs (circRNAs) have been identified; however, their roles have not been fully elucidated. Since dysregulated circRNAs may have clinical applications, it is

Taylor & Francis Group2024-02-20 更新10

Supplementary Table 2 from Inhibition of Protein Kinase C/Twist1 Signaling Augments Anticancer Effects of Androgen Deprivation and Enzalutamide in Prostate Cancer

前列腺癌分子机制

基因表达分析

XLSX file 9K, Ct value of genes in LNCaP and 22Rv1 cells

NIAID Data Ecosystem00

SMAD3 promotes the expression and activity of androgen receptor in prostate cancer [RNA-seq]

前列腺癌分子机制

转录调控

Overexpression of androgen receptor (AR) is the primary cause of castration-resistant prostate cancer, although mechanisms upregulating AR transcription in this context are not well understood. Our RN

NIAID Data Ecosystem10

RNAseq PC3 DMSO vs GW3965. RNAseq PC3 DMSO vs GW3965

前列腺癌分子机制

单细胞RNA测序药物研究

Identify LXR target gens that are involved in migration and invasion phenotype Overall design: PC3 prostate cancer cell were treated for 24h with DMSO or GW3965 1µM in RPMI-1640, L-Glu 2mM after overn

NIAID Data Ecosystem10

The ETS family member GABPa mediates the development of castrate-resistant prostate cancer

资源简介：

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