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Related Concept Videos

Internal Receptors01:31

Internal Receptors

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Many cellular signals are hydrophilic and therefore cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind to internal, or intracellular, receptors that reside within the cell. Many mammalian steroid hormones use this mechanism of cell signaling, as does nitric oxide (NO) gas.
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Enzyme-linked Receptors01:00

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Enzyme-linked receptors are proteins that act as both receptor and enzyme, activating multiple intracellular signals. This is a large group of receptors that include the receptor tyrosine kinase (RTK) family. Many growth factors and hormones bind to and activate the RTKs.
Neurotrophin (NT) receptors are a family of RTKs, including trkA, trkB, and trkC (tropomyosin-related kinase) receptors. TrkA is specific for nerve growth factor (NGF), neurotrophin-6, and neurotrophin-7. TrkB binds...
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Serum Studies: Renal Function Tests01:24

Serum Studies: Renal Function Tests

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Renal function tests are crucial for assessing kidney health, monitoring disease progression, and evaluating the kidneys' efficiency in waste elimination, fluid balance, and electrolyte regulation. These tests offer critical insights into kidney function, even though routine measurements may appear normal until there is a significant decline in the glomerular filtration rate or GFR. Typically, signs of kidney impairment only become evident when the GFR falls to about 50% of its normal level.
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G-protein Coupled Receptors01:21

G-protein Coupled Receptors

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G-protein coupled receptors are ligand binding receptors that indirectly affect changes in the cell. The actual receptor is a single polypeptide that transverses the cell membrane seven times creating intracellular and extracellular loops. The extracellular loops create a ligand specific pocket which binds to neurotransmitters or hormones. The intracellular loops holds onto the G-protein.
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Types of Receptors: Internal Receptors01:07

Types of Receptors: Internal Receptors

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Many cellular signals are hydrophilic and cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind intracellular receptors that reside within the cell cytoplasm or nucleus. Many mammalian steroid hormones and nitric oxide (NO) gas use this cell signaling mechanism.
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Biochemical Reconstitution of Steroid Receptor•Hsp90 Protein Complexes and Reactivation of Ligand Binding
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Functional Studies on Steroid Receptors.

Simon Schlanger1, Hannelore V Heemers2,3,4

  • 1Department of Cancer Biology, Cleveland Clinic, Lerner Research Institute, Cleveland, OH, USA.

Methods in Molecular Biology (Clifton, N.J.)
|May 23, 2018
PubMed
Summary
This summary is machine-generated.

Prostate cancer progression involves altered androgen receptor (AR) coregulators. Modulating these AR-associated proteins with small molecules offers a potential therapeutic strategy for prostate cancer.

Keywords:
Androgen receptorCoregulatory proteinsProstate cancer progressionTranscriptional complexes

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Area of Science:

  • Oncology
  • Molecular Biology
  • Endocrinology

Background:

  • Nuclear receptors are crucial in prostate cancer.
  • The androgen receptor (AR) is a key transcription factor regulating cellular events.
  • AR-associated coregulators can be up- or down-regulated in prostate cancer.

Purpose of the Study:

  • To investigate the role of AR-associated coregulators in prostate cancer.
  • To explore the potential of modulating AR-associated proteins for cancer therapy.

Main Methods:

  • Gene silencing and overexpression techniques.
  • Hormonal treatment.
  • Real-time RT-PCR and Chromatin Immunoprecipitation (ChIP) assays.

Main Results:

  • Altered expression of AR-associated regulators may enhance androgen-induced proliferation, migration, and invasion.
  • Investigated expression and function of AR-associated proteins.

Conclusions:

  • AR-associated coregulators are implicated in prostate cancer development.
  • Targeting AR-associated proteins with small molecule inhibitors presents a promising therapeutic avenue for prostate cancer.