[HTML][HTML] Decoding the androgen receptor splice variants
In the past five years, multiple structurally and functionally distinct androgen receptor (AR)
splice variants have been decoded and characterized. The mature transcripts for the …
splice variants have been decoded and characterized. The mature transcripts for the …
Biologic and clinical significance of androgen receptor variants in castration resistant prostate cancer
KE Ware, MA Garcia-Blanco… - Endocrine-related …, 2014 - erc.bioscientifica.com
As prostate cancer (PCa) progresses to the lethal castration resistant and metastatic form,
genetic and epigenetic adaptation, clonal selection, and evolution of the tumor …
genetic and epigenetic adaptation, clonal selection, and evolution of the tumor …
Androgen receptor variant-driven prostate cancer II: advances in laboratory investigations
C Lu, LC Brown, ES Antonarakis… - Prostate cancer and …, 2020 - nature.com
Background The androgen receptor (AR) is a key prostate cancer drug target. Suppression
of AR signaling mediated by the full-length AR (AR-FL) is the therapeutic goal of all existing …
of AR signaling mediated by the full-length AR (AR-FL) is the therapeutic goal of all existing …
Constitutively active androgen receptor splice variants expressed in castration-resistant prostate cancer require full-length androgen receptor
PA Watson, YF Chen, MD Balbas… - Proceedings of the …, 2010 - National Acad Sciences
Androgen receptor (AR) splice variants lacking the ligand binding domain (ARVs), originally
isolated from prostate cancer cell lines derived from a single patient, are detected in normal …
isolated from prostate cancer cell lines derived from a single patient, are detected in normal …
Role of androgen receptor splice variants, their clinical relevance and treatment options
S Wach, H Taubert, M Cronauer - World journal of urology, 2020 - Springer
Purpose In this review, we summarize the importance of AR variants with a particular focus
on clinically relevant members of this family. Methods A non-systematic literature review was …
on clinically relevant members of this family. Methods A non-systematic literature review was …
[HTML][HTML] Androgen receptor splice variants activating the full-length receptor in mediating resistance to androgen-directed therapy
Upregulation of constitutively-active androgen receptor splice variants (AR-Vs) has been
implicated in AR-driven tumor progression in castration-resistant prostate cancer. To date …
implicated in AR-driven tumor progression in castration-resistant prostate cancer. To date …
Interplay between cytoplasmic and nuclear androgen receptor splice variants mediates castration resistance
Androgen receptor splice variants (AR-V) are implicated in resistance of prostate cancer to
androgen-directed therapies. When expressed alone in cells, some AR-Vs (eg, AR-V7) …
androgen-directed therapies. When expressed alone in cells, some AR-Vs (eg, AR-V7) …
AR splicing variants and resistance to AR targeting agents
Simple Summary Androgen receptor splice variants (AR-Vs) play an important role in
prostate cancer progression, especially as a putative resistance mechanism against AR …
prostate cancer progression, especially as a putative resistance mechanism against AR …
Androgen receptor variant-driven prostate cancer: clinical implications and therapeutic targeting
ES Antonarakis, AJ Armstrong, SM Dehm… - Prostate cancer and …, 2016 - nature.com
While there are myriad mechanisms of primary and acquired resistance to conventional and
next-generation hormonal therapies in prostate cancer, the potential role of androgen …
next-generation hormonal therapies in prostate cancer, the potential role of androgen …
Are androgen receptor variants a substitute for the full-length receptor?
J Lu, TV der Steen, DJ Tindall - Nature reviews urology, 2015 - nature.com
Androgen receptor splice variants (AR-Vs)—which are expressed in castration-resistant
prostate cancer (CRPC) cell lines and clinical samples—lack the C-terminal ligand-binding …
prostate cancer (CRPC) cell lines and clinical samples—lack the C-terminal ligand-binding …