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Androgen receptor activity inversely correlates with immune cell infiltration and immunotherapy response across multiple cancer lineages.
Hu, Ya-Mei; Zhao, Faming; Graff, Julie N; Chen, Canping; Zhao, Xiyue; Thomas, George V; Wu, Hui; Kardosh, Adel; Mills, Gordon B; Alumkal, Joshi J; Moran, Amy E; Xia, Zheng.
Afiliação
  • Hu YM; Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
  • Zhao F; Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
  • Graff JN; Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
  • Chen C; VA Portland Health Care System, Portland, OR, USA.
  • Zhao X; Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
  • Thomas GV; Department of Biomedical Engineering, Oregon Health & Science University, Portland, OR, USA.
  • Wu H; Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
  • Kardosh A; Department of Pathology & Laboratory Medicine, Oregon Health & Science University, Portland, OR, USA.
  • Mills GB; Division of Biomaterial and Biomedical Sciences, Department of Oral Rehabilitation and Biosciences, Oregon Health & Science University, Portland, OR, USA.
  • Alumkal JJ; Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
  • Moran AE; Division of Oncological Sciences, Knight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
  • Xia Z; Department of Internal Medicine, Rogel Cancer Center, University of Michigan, Ann Arbor, MI, USA.
bioRxiv ; 2024 May 14.
Article em En | MEDLINE | ID: mdl-38798471
ABSTRACT
There is now increasing recognition of the important role of androgen receptor (AR) in modulating immune function. To gain a comprehensive understanding of the effects of AR activity on cancer immunity, we employed a computational approach to profile AR activity in 33 human tumor types using RNA-Seq datasets from The Cancer Genome Atlas. Our pan-cancer analysis revealed that the genes most negatively correlated with AR activity across cancers are involved in active immune system processes. Importantly, we observed a significant negative correlation between AR activity and IFNγ pathway activity at the pan-cancer level. Indeed, using a matched biopsy dataset from subjects with prostate cancer before and after AR-targeted treatment, we verified that inhibiting AR enriches immune cell abundances and is associated with higher IFNγ pathway activity. Furthermore, by analyzing immunotherapy datasets in multiple cancers, our results demonstrate that low AR activity was significantly associated with a favorable response to immunotherapy. Together, our data provide a comprehensive assessment of the relationship between AR signaling and tumor immunity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos