Target intelligence / Profile preview

Progesterone receptor and Androgen receptor

Molecular classification
Receptor, Nuclear receptor, Transcription factor, Steroid hormone receptor
01

Overview

The 'Progesterone receptor and Androgen receptor' is an incorrect grouping for a single therapeutic target. Both Progesterone receptor (PR) and Androgen receptor (AR) are distinct members of the steroid hormone nuclear receptor family, sharing structural homology and a common mechanism of action as transcription factors. However, they are activated by different ligands (progesterone for PR; androgens for AR) and mediate distinct biological functions, primarily governing female and male reproductive biology, respectively. They are individually critical therapeutic targets in various hormone-dependent cancers (e.g., PR in breast and endometrial cancer, AR in prostate cancer) and endocrine disorders. While related in their classification, their specific roles and therapeutic interventions warrant separate consideration.

Other names
PR and ARNuclear receptor subfamily 3 group C member 3 and Nuclear receptor subfamily 3 group C member 4NR3C3 and NR3C4
02

Mechanism of action

Both are nuclear receptors that bind specific steroid hormones (progesterone for PR, androgens for AR) to regulate gene expression. Agonists stimulate their transcriptional activity, while antagonists block hormone binding or receptor function, thus suppressing downstream gene transcription specific to each receptor.

03

Biological functions

Regulation of gene transcriptionSignal transductionCell growth and differentiationReproductive tissue development and maintenance (PR)Male sexual development and maintenance (AR)
04

Disease associations

Cancer (e.g., breast cancer, prostate cancer, endometrial cancer, ovarian cancer)Reproductive disorders (e.g., androgen insensitivity syndromes, infertility)Benign prostatic hyperplasiaOther hormone-related diseases
05

Safety considerations

Off-target hormone effects due to lack of specificityHormonal imbalanceIncreased cancer risk (reproductive tissues) with certain hormonal therapiesThromboembolic complications (some progestins)Cardiac or metabolic adverse eventsResistance mutations in cancer treatments
06

Interacting drugs

Mifepristone (targets PR)

4 more in the full profile.

07

Biomarkers

PR expression for breast and endometrial cancer prognostics and therapy selectionAR abundance and mutations for prostate cancer management and antiandrogen therapy selection

Beyond the preview

Go deeper on Progesterone receptor and Androgen receptor.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Progesterone receptor and Androgen receptor.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call