Inhibition of signaling downstream of beta-2 adrenoceptor by propranolol in prostate cancer cells.


Journal

The Prostate
ISSN: 1097-0045
Titre abrégé: Prostate
Pays: United States
ID NLM: 8101368

Informations de publication

Date de publication:
02 2023
Historique:
revised: 07 06 2022
received: 18 08 2021
accepted: 04 07 2022
pubmed: 15 11 2022
medline: 11 1 2023
entrez: 14 11 2022
Statut: ppublish

Résumé

There is accumulating evidence that propranolol, an antagonist of beta-1 and beta-2 adrenoreceptors, extends survival of patients with prostate cancer; yet it is not known whether propranolol inhibits beta-adrenergic signaling in prostate cancer cells, or systemic effects of propranolol play the leading role in slowing down cancer progression. Recently initiated clinical studies offer a possibility to test whether administration of propranolol inhibits signaling pathways in prostate tumors, however, there is limited information on the dynamics of signaling pathways activated downstream of beta-2 adrenoreceptors in prostate cancer cells and on the inactivation of these pathways upon propranolol administration. Western blot analysis was used to test the effects of epinephrine and propranolol on activation of protein kinase (PKA) signaling in mouse prostates and PKA, extracellular signal-regulated kinase (ERK), and protein kinase B/AKT (AKT) signaling in prostate cancer cell lines. In prostate cancer cell lines epinephrine induced robust phosphorylation of PKA substrates pS133CREB and pS157VASP that was evident 2 min after treatments and lasted for 3-6 h. Epinephrine induced phosphorylation of AKT in PTEN-positive 22Rv1 cells, whereas changes of constitutive AKT phosphorylation were minimal in PTEN-negative PC3, C42, and LNCaP cells. A modest short-term increase of pERK in response to epinephrine was observed in all tested cell lines. Incubation of prostate cancer cells with 10-fold molar excess of propranolol for 30 min inhibited all downstream pathways activated by epinephrine. Subjecting mice to immobilization stress induced phosphorylation of S133CREB, whereas injection of propranolol at 1.5 mg/kg prevented the stress-induced phosphorylation. The analysis of pS133CREB and pS157VASP allows measuring activation of PKA signaling downstream of beta-2 adrenoreceptors. Presented results on the ratio of propranolol/epinephrine and the time needed to inhibit signaling downstream of beta-2 adrenoreceptors will help to design clinical studies that examine the effects of propranolol on prostate tumors.

Sections du résumé

BACKGROUND
There is accumulating evidence that propranolol, an antagonist of beta-1 and beta-2 adrenoreceptors, extends survival of patients with prostate cancer; yet it is not known whether propranolol inhibits beta-adrenergic signaling in prostate cancer cells, or systemic effects of propranolol play the leading role in slowing down cancer progression. Recently initiated clinical studies offer a possibility to test whether administration of propranolol inhibits signaling pathways in prostate tumors, however, there is limited information on the dynamics of signaling pathways activated downstream of beta-2 adrenoreceptors in prostate cancer cells and on the inactivation of these pathways upon propranolol administration.
METHODS
Western blot analysis was used to test the effects of epinephrine and propranolol on activation of protein kinase (PKA) signaling in mouse prostates and PKA, extracellular signal-regulated kinase (ERK), and protein kinase B/AKT (AKT) signaling in prostate cancer cell lines.
RESULTS
In prostate cancer cell lines epinephrine induced robust phosphorylation of PKA substrates pS133CREB and pS157VASP that was evident 2 min after treatments and lasted for 3-6 h. Epinephrine induced phosphorylation of AKT in PTEN-positive 22Rv1 cells, whereas changes of constitutive AKT phosphorylation were minimal in PTEN-negative PC3, C42, and LNCaP cells. A modest short-term increase of pERK in response to epinephrine was observed in all tested cell lines. Incubation of prostate cancer cells with 10-fold molar excess of propranolol for 30 min inhibited all downstream pathways activated by epinephrine. Subjecting mice to immobilization stress induced phosphorylation of S133CREB, whereas injection of propranolol at 1.5 mg/kg prevented the stress-induced phosphorylation.
CONCLUSIONS
The analysis of pS133CREB and pS157VASP allows measuring activation of PKA signaling downstream of beta-2 adrenoreceptors. Presented results on the ratio of propranolol/epinephrine and the time needed to inhibit signaling downstream of beta-2 adrenoreceptors will help to design clinical studies that examine the effects of propranolol on prostate tumors.

Identifiants

pubmed: 36373761
doi: 10.1002/pros.24455
pmc: PMC10100053
doi:

Substances chimiques

Propranolol 9Y8NXQ24VQ
Proto-Oncogene Proteins c-akt EC 2.7.11.1
Epinephrine YKH834O4BH

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

237-245

Subventions

Organisme : NCI NIH HHS
ID : P30 CA012197
Pays : United States

Informations de copyright

© 2022 The Authors. The Prostate published by Wiley Periodicals LLC.

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Auteurs

Aljoharah Alaskar (A)

Department of Life Sciences and Life Sciences Program, Alfaisal University, Riyadh, Saudi Arabia.

Amaal Abdulraqeb Ali (A)

Department of Life Sciences and Life Sciences Program, Alfaisal University, Riyadh, Saudi Arabia.

Sazzad Hassan (S)

Indiana University School of Medicine-South Bend, South Bend, Indiana, USA.

Zakia Shinwari (Z)

Stem Cell & Tissue Re-Engineering Program, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

Ayodele Alaiya (A)

Stem Cell & Tissue Re-Engineering Program, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

Urs von Holzen (U)

Indiana University School of Medicine-South Bend, South Bend, Indiana, USA.
Goshen Center for Cancer Care, Goshen, Indiana, USA.

Lance Miller (L)

Department of Cancer Biology, Comprehensive Cancer Center, Winston-Salem, North Carolina, USA.
Department of Urology, Wake Forest University Health Sciences, Winston-Salem, North Carolina, USA.

George Kulik (G)

Department of Life Sciences and Life Sciences Program, Alfaisal University, Riyadh, Saudi Arabia.
Department of Cancer Biology, Comprehensive Cancer Center, Winston-Salem, North Carolina, USA.
Department of Urology, Wake Forest University Health Sciences, Winston-Salem, North Carolina, USA.

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