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Human androgen receptor ligand-binding domain complex with modulator (PDB code 3b5r)

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The androgen receptor (AR) belongs to the steroid hormone group nuclear receptor family with the estrogen, progesterone, glucocorticoid and mineralcorticoid receptor.

AR mediate the actions of testosterone (T) and a more biologically active form, 5α-dihydrotestosterone (DHT), which are the male sex hormones required for development of the male reproductive system and secondary sexual characteristics. This receptor, located on the X chromosome, is expressed in a diverse range of tissues, because they have significant biological actions in many systems ^[1]. There are other androgens that bind with much less potency than T and DHT such as androstenedione, androstenediol, and dehydroepiandrosterone (DHEA) ^[2].

Structure

Like members of the nuclear receptor family, the AR consists of three main functional domains which aid in controlling and regulating transcriptional activity.

Domains

N-terminal Domain (NTD)(residues 1-555)

This region is required for full transcriptional activity ^[3], because of its necessary presence for Ligand-Binding Domain (LBD) activation ^[4]. The sequence and lengths of the polyglutamine (CAG) and polyglycine (GGC) repeats are highly variable in the human population, making this the most variable domain. It has been shown that the length of the CAG repeat region affects the folding and structure of this domain. Shorter repeats generally impose a higher AR transactivation activity, whereas longer repeats cause reduced activity ^[3]. In healthy people, one region of the AR gene shows up to 36 repeats of the CAG sequence. Patients with abnormally high numbers of CAG repeats can develop spinal muscular atrophy.

DNA-Binding Domain (DBD) (residues 555-623)

DBD is a cysteine-rich region that is the most highly conserved in the steroid hormone nuclear receptor family ^[3], but it has been shown that binding of selective androgen response elements (AREs) allow the specific activation functions of the AR. They facilitate direct DNA binding of the AR to the promoter and enhancer regions of AR-regulated genes, thereby allowing the activation functions of the N-terminal and LBD to stimulate or repress the transcription of these genes ^[1].

AR is a dimer, like other steroid receptors, consisting of two equal, common hexameric half-sites, separated by a 3 base-pair spacer ^[3]. This domain is critical for AR function, due to its role in dimerization and binding of dimerized AR to select motifs on target DNA ^[4].

Each DBD monomer has a core composed of two zinc finger motifs, which consists of four cysteine residues that coordinate a zinc ion ^[3]. The first one is closer to the NTD which has the P box, identical in all the family, that controls the DNA binding specificity at AREs ^[4]. The second zinc finger motif facilitates AR dimerization via the D box.

Additionally, a nuclear localisation signal (NLS) is localised at the junction between the DBD and the hinge region, it binds to importin-α and facilitates nuclear translocation ^[4]. Passive transport across the nuclear pore complex has been suggested ranging from 20–40 kDa, in contrast, the AR, which is 110 kDa in size, requires help to be actively transported upon ligand binding ^[3].

The DBD is linked to the LBD by a flexible hinge region (residues 623-665), which is a linker poorly conserved. Once in the nucleus, this region also interacts with the DBD to identify specific sequences for AR binding. It controls the AR activation and degradation. Consequently, mutations in the hinge region can lead to enhanced AR potency ^[4].

Ligand-Binding Domain (LBD) (residues 665-919)

The LBD, located at the C-terminal, is the main target of AR inhibitors ^[4]. It consists of eleven α-helixes in the ligand binding pocket ( active site ) , with reposition upon androgen binding, converting into the activation function 2 (AF-2) domain. Unlike other nuclear receptors, the AR does not have H2, which is instead replaced by a long flexible linker ^[3]. The LBD binds to motifs in the NTD and in AR-specific cofactors and coactivators. Moreover, LBD-LBD homodimerization of AR is essential in the proper functioning of the receptos ^[4]. This domain has been structurally well characterized by crystallography and a number of mutations have been identified. It is important because not all mutations affect ligand binding, but some of them may disrupt androgen induced interaction of the N-terminal motif and C-terminal AF-2 ^[4].

Transcriptional Activation Function

Two transcriptional activation functions have been identified:

The ligand-independent AF-1 (residues 142-485): located in the NTD is constitutively active. It is the main region responsible for mediating AR transcription. Its contains two separable transcription activation units that are indispensable for full activity of the AR ^[3].
The ligand-dependent AF-2: is located in the LBD ^[1]. Helix 12 (H12) forms the core of this region and acts as a lid to close the LBD upon agonist binding ^[3]. It is important for forming the coregulator bindings site as well as mediating direct interactions between the N-terminal and LBD. Key differences in the contribution of specific conserved residues in the AF-2 core domain between the AR and other steroid hormone nuclear receptors have been identified, it would explain the differences in the structure and the function, as well as the coregulatory proteins they interact with ^[1].

Mechanism of Action

AR signaling

AR has two mechanisms of action: the DNA binding-dependent (genomic AR signaling) and the DNA binding independent (non-genomic AR signaling).

Reproduced from Davey & Grossmann. ^[1]

DNA-Binding dependent actions of the AR

Reproduced from Tan et al. ^[3]

In the absence of ligand, the AR is in the cytoplasm and associated with heat-shock and other chaperone proteins. Testosterone is converted into DHT by 5α-reductase, with higher affinity to bind the receptor. When DHT binds AR, it displaces heat shock proteins, drives the interaction between the N- and C-terminal, and binds importin-α to translocate the ligand/AR complex into the nucleus.

In the nucleus, the receptor dimerizes and binds to AREs in the promoter regions of target genes. At the promoter, the AR is able to recruit members of the basal transcription machinery in addition to other coregulators to facilitate transcription ^[3].

AR activity is not only regulated by ligand binding and DNA binding but also by intramolecular interactions between functional domains, by homodimerization and by interactions with cofactors ^[5]. This leads to the initiation of transcription, cell proliferation and survival, and negative feedback to inactivate AR transcription ^[1].

Non-DNA Binding dependent actions of the AR

It has been shown that the androgen/AR complex activates 2nd messenger pathways including ERK, Akt and MAPK, and it also interferes with several key proteins including forkhead box protein A1 (FOXA1), PI3K and receptor tyrosine kinases. These effects occur within seconds to minutes of androgen treatment ^[1]^[6].

There are studies suggesting that some of the non-DNA binding-dependent actions of androgens are mediated via the activation of membrane-bound protein receptors. For instance, the iron-regulated transporter-like protein 9 (ZIP9) mediates the androgen-induced apoptosis of ovarian follicle cells, prostate and breast cancer cells ^[1].

Although the physiological significance of the non-DNA binding-dependent actions of the AR is not yet fully defined, it has been proposed they may oppose the DNA binding-dependent actions and serve as a brake to fine-tune androgen action in target tissues ^[1].

Ligand-Independent actions of the AR

It has been demonstrated that AR has the potential to be activated through ligand-independent mechanisms by a number of different growth factors, via phosphorylation of the AR or following interaction with co-activators ^[1].

Function

As AR is expressed in many tissues, androgens have been documented to have significant biological actions in bone, muscle, prostate, ovaries, endometrium, bladder, skin, cardiovascular, immune, neural and hematopoietic systems ^[1]^[7]. Androgens have a role in behavior and cognition in neuronal cells in the CNS ^[7]. It has also been shown they regulate hair growth, sebum production and secretion, wound healing and cutaneous barrier formation in the skin ^[8]. The absence of AR has an impact on the fertility in granulosa cells in the ovary and it also affects the myometrial cell growth in uterine glandular epithelial cells in the endometrium ^[7].

Diseases

Drugs targeting the AR has the potential to be used in prostate cancer, benign prostatic hyperplasia (BPH), osteoporosis, breast cancer, hypogonadism, conditions where cachexia is a consequence of the disease state (HIV, cancer, immobilization), urinary incontinence, muscle wasting conditions as Duchenne muscular dystrophy (DMD) and Alzheimer’s disease ^[9]^[10]^[11]^[12].

Prostate Cancer

AR is fundamental for the correct function and development of the prostate ^[13], having a critical role in the control of homeostasis between prostate cells differentiation and proliferation ^[14]. It's widely accepted this receptor plays an important role in prostate cancer cells due to the alteration of that equilibrium, shifting the AR to a more proliferative transcriptional program ^[14].

Alzheimer’s Disease

Androgen depletion is considered a significant risk factor for Alzheimer’s disease, and circulating testosterone levels are inversely correlated with levels of ß-amyloid (ßA) in the brains of aged men ^[9].

Pharmacology

Steroid

Natural ligand: Testosterone

Aging and other factors are associated with a reduction of testosterone levels which could lead to late onset hypogonadism ^[15]. The decrease of the T levels and therefore its active metabolite levels (DHT) are related with several symptoms such as low libido, erectile dysfunction, skeletal muscular loss ^[10]^[15], increased cardiovascular risk ^[15], etc. To treat those symptoms is used Testosterone Restitution Therapy (TRT) which has been associated with the improvement in sexual function and the increase in muscle mass and bone mineral density ^[16].

One of the problems associated with the use of T as a therapeutic agent in TRT is the delivery method, tending to have low efficacy orally administered ^[10]^[11], and having some inconvenients with intramuscular injections or implants ^[10]. Also, the use of this hormone as a treatment could triggered a lot of AR widespread around the body. Long-term exposures to a high dose could lead to related side effects like erythrocytosis ^[10]^[11], dyslipidemia, hepatotoxicity ^[11] and an increase in cardiovascular risk ^[15]^[16].

Due to all these problems, some institutions like the FDA warn about the safety issues related with this therapy assessing the reduction of its use ^[15]^[16]. However, other agencies like the EMA supported by the European Academy of Andrology establish the practical use of this therapy in men’s hypogonadism ^[15]^[16]. So, there is still some controversy about its use, and it’s still currently studied in clinical trials ^[16].

Human androgen receptor bound to testosterone (2ylo).

Antagonist: Steroid ARA

The development of these drugs were one of the first approaches to treat prostate cancer, targeting AR activity by having a structure with an steroidal skeleton ^[14]. This kind of antiandrogens have another steroid receptor affinity (glucocorticoids receptor, progesterone receptor…) having low efficiency and some side effects like hepatotoxicity and increased cardiovascular risks ^[14]. Some examples are cyproterone acetate (CPA) ^[14]^[17]^[18] or megestrol acetate ^[14].

Agonist: Anabolic Androgen Steroids (AAs)

Reproduced from Sessa et al. ^[19]

These drugs have been produced since the middle of the 20th century ^[20]. They have anabolic activity which improves muscular mass and physical function. However, their uncontrolled use and abuse lead to several side effects like: testicular atrophy, alopecia, gynecomastia in the case of males, and clitoral hypertrophy, menstrual irregularities in the case of women. Men and women can experience mood disorders and the chronic abuse could result in high risk of suffering cardiovascular disease and prostate cancer ^[20].

Because of the doping scandals in the athlete community, the World Anti-Doping Agency (WADA) has prohibited them ^[20]. This creates the need to discover androgens that have beneficial anabolic activity with reduced androgenic activity.

Non-Steroid

Selective Androgen Receptor Modulators (SARMs)

Steroid androgens can be associated with a high rate of adverse effects, which limits their widespread clinical use. To overcome these side effects, SARMs were developed. They are small molecule drugs that manipulate the AR function in different tissues ^[9], acting as both agonist and antagonist, making them potential to treat AR-related diseases.

These non-steroidal drugs normally can be administered orally or using a transdermal injection ^[10]^[11], having better compliance. They are not affected by 5α-reductase (limiting its androgenic risk effects) and aromatase (limiting its estrogenic risk effects) ^[10]^[11]. Those characteristics help to the reduction of side effects related with the use of natural androgens. Moreover, the tissue selectivity of these drugs make them a suitable option to treat a great group of diseases skipping the risk related with the use of TRT ^[10]^[11]^[12].

Also, some SARMs could be a suitable option to achieve the improvement in anabolic activity and muscular density obtained by the use of AAs, without the unwanted side effects associated with their androgenic action ^[20].

Mechanism of SARMs

Currently SARMs tissue selectivity is still under research ^[12]^[20] and there is no consensus in the mechanisms of action. However, there are two hypotheses that could explain it:

Their non-steroidal composition and the fact that they are unaffected by 5α-reductase ^[11]^[12]^[20], which promote the interaction of AR with tissue-specific coactivators.
The way SARMs bind to the AR, which is what primarily enhances or represses their effect. Each SARMs/AR complex has a different conformation and tissues have unique patterns of AR expression, co-regulatory proteins levels and transcriptional regulation ^[9].

When a ligand promotes interactions between the N- and C-terminal AR domains, the AR is maximally active. The ability to reduce N/C interactions is the hallmark of SARMs that display antagonisms in androgenic tissues ^[9].

Diseases that could be treated with SARMs

SARMs may one day play a role in the treatment of cognitive disorders, such as Alzheimer's disease. Androgens facilitate the reduction of deleterious ß-amyloid (ßA) plaques, upregulating the expression of ßA-degrading neprilysin and they promote synapse formation and neurogenesis, upregulating brain derived neurotrophic factor ^[20]. AR in breast cancer likely confers survival advantage by modulating ER signaling, which may reduce the risk of metastasis and aggressive disease. There is a clinical trial seeking to evaluate pembrolizumab and enobosarm co-therapy for the treatment of AR positive metastatic triple negative breast cancer ^[9]. Urinary incontinence denotes involuntary bladder urine leakage amongst women commonly with decreased pelvic muscle strength. As the pelvic floor muscles contain high levels of AR, it is a relevant target for SARM therapy ^[20].

Side effects

Despite the consistent effect demonstrated by SARMs on lean body mass accrual, reductions in high-density lipoprotein (HDL) with even low doses seem to be an important concern with these compounds, though it occurs to a lesser extent compared to testosterone ^[21]. SARMs administration has also been related to hepatotoxicity and some compounds have shown liver enzymes alterations, the most common adverse events being increases in alanine transaminase and aspartate transaminase ^[21]. The anabolic effects of SARMs and their lack of androgenic side effects have made them of great interest to the bodybuilding community and create the potential for abuse among competitive athletes ^[9].

Antagonist

These kinds of drugs were developed with the objective to avoid the secondary effects associated with cross reactivity of steroidal ARA, increasing the selectivity and the affinity to the androgen receptor, limiting the association with other steroids nuclear receptors ^[17]. Also, their non-steroidal structure improved oral bioavailability being another advantage in comparison with steroidal ARA ^[17]. Some examples are flutamide, bicalutamide ^[14]^[17]^[18]^[22]^[23]^[24] or apalutamide (ARN-509) ^[14]^[24].

Bicalutamide

R-Bicalutamide, marketed as Casodex ^[14]^[18], is one of the most stable and tolerated androgen receptor antagonists used in the treatment of prostate cancer ^[14]^[17]^[25], belonging to the first generation of antiandrogens developed ^[14]^[26]. It is a competitive antagonist ^[22]^[26]^[25] which binds to the LBD producing a transcriptionally inactive androgen receptor ^[22]. However, it seems that the long-term use of these drugs and other first generation antiandrogens leads to withdrawal syndrome in prostate cancer resistant to castration patients ^[14]^[18]. In many cases associated androgen receptor mutations like W741L that can switch the mechanism of action of the drug from antagonist to agonist or partial agonist ^[14]^[17]^[18]^[23]^[26]. Although bicalutamide has been patented since 1982 and approved to be clinical used by the FDA since 1995 ^[17], its mechanism of action it's still a debate, because the X-ray structure of the wild-type androgen receptor binded to an antagonist is not yet solved ^[26]. Changes in the conformation of the androgen receptor due to association with antagonists have been hypothesized to be similar to those produced in the steroid receptor family ^[14]^[26]. When an agonist or a ligand binds to the LBD it seems that it induces a conformation of the steroid receptor which makes H12 close off the pocket of LBD allowing the union of cofactors so, at the end, permitting the steroid receptor function allowing the DNA transcription ^[14]. Although, when an antagonist is binded, H12 seems to be more separated to the LBD, disabling the binding of coactivators ^[14] and the migration of the nuclear receptor into the nucleus ^[26]. Nonetheless, the AR has some structural singularities that may not let this change of conformation, being the most important the additional C-terminal region in H12 anchored to the receptor by the formation of a ß-sheet, limiting its movement ^[14]^[26]. Due to this structural difference, in silico approaches have suggested that the antiandrogen effect of bicalutamide may be produced by the instability of the homodimer ^[26]. That may lend to the homodimer dissociation preventing the transcriptional activity of the AR explaining the mechanism of action of this drug ^[26]. Also, in silico analysis have shown that the W741L mutation leads to a bicalutamide-AR homodimer more stable, which may make some insight into the withdrawal syndrome observed in bicalutamide treatment ^[26]. It is mandatory to understand by future research the whole mechanism of action of the current antiandrogens clinically used, with the objective of developing new drugs which can escape to the antagonist-agonist switch seen by bicalutamide, or other antiandrogens like flutamide. One example of this is apalutamide, a non-steroidal second generation antiandrogen ^[14]^[24] approved for use in non metastatic castration resistant prostate cancer patients by the FDA in 2018 ^[24]. See also the SPARTAN study^[27]. This new drug has promising uses but it is still associated with side effects like an increased level of falls in patients with the treatment vs placebo ^[28].

3D Structures of androgen receptor

Androgen receptor 3D structures

References

Proteopedia Page Contributors and Editors (what is this?)

Cristina Benito, Michal Harel, Alexander Berchansky, Cristina Murga, Wayne Decatur, Marta Roldan Lazaro, Joel L. Sussman, David Sánchez Fernández

[Bench_to_Bedside-1] 1.00 ^1.01 ^1.02 ^1.03 ^1.04 ^1.05 ^1.06 ^1.07 ^1.08 ^1.09 ^1.10 Davey RA, Grossmann M. Androgen Receptor Structure, Function and Biology: From Bench to Bedside. Clin Biochem Rev. 2016 Feb;37(1):3-15. PMID:27057074

[2] Kolyvas EA, Caldas C, Kelly K, Ahmad SS. Androgen receptor function and targeted therapeutics across breast cancer subtypes. Breast Cancer Res. 2022 Nov 14;24(1):79. doi: 10.1186/s13058-022-01574-4. PMID:36376977 doi:https://dx.doi.org/10.1186/s13058-022-01574-4

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[AR-4] 4.0 ^4.1 ^4.2 ^4.3 ^4.4 ^4.5 ^4.6 ^4.7 Messner EA, Steele TM, Tsamouri MM, Hejazi N, Gao AC, Mudryj M, Ghosh PM. The Androgen Receptor in Prostate Cancer: Effect of Structure, Ligands and Spliced Variants on Therapy. Biomedicines. 2020 Oct 15;8(10):422. doi: 10.3390/biomedicines8100422. PMID:33076388 doi:https://dx.doi.org/10.3390/biomedicines8100422

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@@ Line 80: / Line 80: @@
 ===Agonist: Anabolic Androgen Steroids (AAs)===
-'''[[Image:Side effects.jpg | thumb | upright=2.0 | Reproduced from Tessa et al. <ref>PMID: 30524281</ref> ]]'''
+'''[[Image:Side effects.jpg | thumb | upright=2.0 | Reproduced from Sessa et al. <ref>PMID: 30524281</ref> ]]'''
 These drugs have been produced since the middle of the 20th century <ref name="Steroids">PMID: 33148520</ref>. They have anabolic activity which improves muscular mass and physical function. However, their uncontrolled use and abuse lead to several side effects like: testicular atrophy, alopecia, gynecomastia in the case of males, and clitoral hypertrophy, menstrual irregularities in the case of women. Men and women can experience mood disorders and the chronic abuse could result in high risk of suffering cardiovascular disease and prostate cancer <ref name="Steroids" />.
 Because of the doping scandals in the athlete community, the World Anti-Doping Agency (WADA) has prohibited them <ref name="Steroids" />. This creates the need to discover androgens that have beneficial anabolic activity with reduced androgenic activity.
@@ Line 87: / Line 88: @@
 ===Selective Androgen Receptor Modulators (SARMs)===
 Steroid androgens can be associated with a high rate of adverse effects, which limits their widespread clinical use. To overcome these side effects, SARMs were developed.
-SARMs are small molecule drugs that manipulate the AR function in different tissues <ref name="SARMs knowledge" />. They can act as both agonist and antagonist, making them potential to treat AR-related diseases.
+They are small molecule drugs that manipulate the AR function in different tissues <ref name="SARMs knowledge" />, acting as both agonist and antagonist, making them potential to treat AR-related diseases.
-These non-steroidal drugs normally can be administered orally or using a transdermal injection <ref name="NR" /><ref name="SARMs therapy" /> having better compliance and there are not affected by 5α-reductase (limiting its androgenic risk effects) and aromatase (limiting its estrogenic risk effects) <ref name="NR" /><ref name="SARMs therapy" />. Those characteristics help to the reduction of side effects related with the use of natural androgens and the tissue selectivity of these drugs make them a suitable option to treat a great group of diseases skipping the risk related with the use of TRT <ref name="NR" /><ref name="SARMs therapy" /><ref name="SARMs" />.
-Also, some SARMs could be a suitable option to achieve the improvement in anabolic activity and muscular density obtained by the use of AAs without the unwanted side effects associated with their androgenic action of those drugs <ref name="Steroids" />.
+These non-steroidal drugs normally can be administered orally or using a transdermal injection <ref name="NR" /><ref name="SARMs therapy" />, having better compliance. They are not affected by 5α-reductase (limiting its androgenic risk effects) and aromatase (limiting its estrogenic risk effects) <ref name="NR" /><ref name="SARMs therapy" />. Those characteristics help to the reduction of side effects related with the use of natural androgens. Moreover, the tissue selectivity of these drugs make them a suitable option to treat a great group of diseases skipping the risk related with the use of TRT <ref name="NR" /><ref name="SARMs therapy" /><ref name="SARMs" />.
+Also, some SARMs could be a suitable option to achieve the improvement in anabolic activity and muscular density obtained by the use of AAs, without the unwanted side effects associated with their androgenic action <ref name="Steroids" />.
 ====Mechanism of SARMs====
-Currently SARMs tissue selectivity is still under research <ref name="SARMs" /><ref name="Steroids" />. There is no consensus on SARMs mechanisms of action. However, there are two hypotheses that could explain it:
+Currently SARMs tissue selectivity is still under research <ref name="SARMs" /><ref name="Steroids" /> and there is no consensus in the mechanisms of action. However, there are two hypotheses that could explain it:
-It could be related with their non-steroidal composition and with the fact that they are unaffected by 5α-reductase <ref name="SARMs therapy" /><ref name="SARMs" /><ref name="Steroids" /> which promotes the interaction of AR with tissue-specific coactivators.
+*Their non-steroidal composition and the fact that they are unaffected by 5α-reductase <ref name="SARMs therapy" /><ref name="SARMs" /><ref name="Steroids" />, which promote the interaction of AR with tissue-specific coactivators.
-The way SARMs bind to the AR is what primarily enhances or represses their effect. Each SARM-AR complex has a different conformation and tissues have unique patterns of AR expression, co-regulatory proteins levels and transcriptional regulation <ref name="SARMs knowledge" />.
+*The way SARMs bind to the AR, which is what primarily enhances or represses their effect. Each SARMs/AR complex has a different conformation and tissues have unique patterns of AR expression, co-regulatory proteins levels and transcriptional regulation <ref name="SARMs knowledge" />.
 When a ligand promotes interactions between the N- and C-terminal AR domains, the AR is maximally active. The ability to reduce N/C interactions is the hallmark of SARMs that display antagonisms in androgenic tissues <ref name="SARMs knowledge" />.
 ====Diseases that could be treated with SARMs====

Androgen receptor: Difference between revisions