Evidence map›Paper›PMID 34284799›Full record

ReviewCell communication and signaling : CCS2021

Role of α- and β-adrenergic signaling in phenotypic targeting: significance in benign and malignant urologic disease.

M Archer, N Dogra, Z Dovey, T Ganta, H-S Jang, J A Khusid, A Lantz, M Mihalopoulos, J A Stockert, A Zahalka and 15 more

Open access · goldAbstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.9field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Review
  3. Neuroscience in prostate cancer.Prostate cancer and prostatic diseases · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. A Bioactive Benzyl Terpene fromMolecules (Basel, Switzerland) · 2026
    Article
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  9. Article
  10. Review
  11. Article
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors at 4 institutions in 2 countries.

M Archer *Department of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
N Dogra *Department of Pathology and Molecular and Cell Based Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Z Dovey *Department of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
T Ganta *Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
H-S Jang *Department of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
J A Khusid *Department of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
A Lantz *Department of Molecular Medicine and Surgery, Section of Urology, Karolinska Institute, Stockholm, Sweden.
M Mihalopoulos *Department of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
J A Stockert *Department of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
A Zahalka *Department of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
L BjörneboDepartment of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.
S GaglaniDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
M R NohDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
S A KaplanDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
R MehrazinDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
K K BadaniDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
P WiklundDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
K TsaoTisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
D J LundonDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
N MohamedDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
F LucienDepartment of Urology, Mayo Clinic, Rochester, MN, USA.
B PadanilamDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
M GuptaDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
A K TewariDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA.
N KyprianouDepartment of Urology, Icahn School of Medicine at Mount Sinai, 6th Floor, 1425 Madison Avenue, New York, NY, 10029, USA. natasha.kyprianou@mountsinai.org.ORCID 0000-0002-8713-3599
Icahn School of Medicine at Mount Sinai · USKarolinska Institutet · SEMount Sinai Hospital · USMayo Clinic in Arizona · US

Funding

Extracellular Vesicle-Encapsulated AAVs for Therapeutic Gene Delivery to the HeartR01HL148786 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Kiyotake Ishikawa, Susmita Sahoo · 2019 to 2026
$4.1M
Treatment-Induced Phenotypic Reprogramming in Prostate CancerR01CA232574 · NCI · UNIVERSITY OF KENTUCKY · PI KYPRIANOU, NATASHA · 2019 to 2023
$2.2M
Development of siRNA conjugates for combination treatment of acute kidney injuryR01DK120533 · NIDDK · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI OUPICKY, DAVID, PADANILAM, BABU JOSEPH · 2018 to 2022
$2.1M
Neuromodulation of long-term sequelae of ischemic acute kidney injuryR01DK120846 · NIDDK · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PADANILAM, BABU JOSEPH · 2020 to 2023
$1.9M
Reno-protective mechanisms of EETs in acute and chronic obstructive nephropathyR01DK116987 · NIDDK · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PADANILAM, BABU JOSEPH · 2019 to 2022
$1.7M
Novel Approach to Enhance Ostomy Care in Patients with Bladder and Colorectal CancerR21NR016518 · NINR · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MOHAMED, NIHAL · 2017 to 2018
$475k
NCI NIH HHS R01 CA232574NHLBI NIH HHS R01 HL148786NIDDK NIH HHS R01 DK116987NIDDK NIH HHS R01 DK120533NIDDK NIH HHS R01 DK120846NINR NIH HHS R21 NR016518
6 · The paper itself

Abstract

The urinary tract is highly innervated by autonomic nerves which are essential in urinary tract development, the production of growth factors, and the control of homeostasis. These neural signals may become dysregulated in several genitourinary (GU) disease states, both benign and malignant. Accordingly, the autonomic nervous system is a therapeutic target for several genitourinary pathologies including cancer, voiding dysfunction, and obstructing nephrolithiasis. Adrenergic receptors (adrenoceptors) are G-Protein coupled-receptors that are distributed throughout the body. The major function of α1-adrenoceptors is signaling smooth muscle contractions through GPCR and intracellular calcium influx. Pharmacologic intervention of α-and β-adrenoceptors is routinely and successfully implemented in the treatment of benign urologic illnesses, through the use of α-adrenoceptor antagonists. Furthermore, cell-based evidence recently established the antitumor effect of α1-adrenoceptor antagonists in prostate, bladder and renal tumors by reducing neovascularity and impairing growth within the tumor microenvironment via regulation of the phenotypic epithelial-mesenchymal transition (EMT). There has been a significant focus on repurposing the routinely used, Food and Drug Administration-approved α1-adrenoceptor antagonists to inhibit GU tumor growth and angiogenesis in patients with advanced prostate, bladder, and renal cancer. In this review we discuss the current evidence on (a) the signaling events of the autonomic nervous system mediated by its cognate α- and β-adrenoceptors in regulating the phenotypic landscape (EMT) of genitourinary organs; and (b) the therapeutic significance of targeting this signaling pathway in benign and malignant urologic disease. Video abstract.

Indexed as

Adrenergic beta-AntagonistsEpithelial-Mesenchymal TransitionHumansMaleProstateReceptors, Adrenergic, alpha-1Receptors, Adrenergic, beta-1Signal TransductionTumor MicroenvironmentUrinary TractUrologic DiseasesUrologic NeoplasmsADRB1 protein, humanAdrenergic beta-AntagonistsReceptors, Adrenergic, alpha-1Receptors, Adrenergic, beta-1AdrenoceptorsCell polarityFibrosisKidney diseasePhenotypic landscapeUrologic tumorsα- and β-adrenergic blockade

Identifiers

PMID34284799
PMCPMC8290582
OpenAlexW3186768796

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.