Role of histamine H4 receptor in breast cancer cell proliferation

In order to better understand the role of histamine H4 (H4R) receptor in breast cancer, we studied the receptor expression pattern, associated signal transduction pathway and biological responses, in breast cancer cell lines with different malignant characteristics. A different pattern of protein ex...

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Publicado: 2011
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19450494_v3E_n3_p1042_Medina
http://hdl.handle.net/20.500.12110/paper_19450494_v3E_n3_p1042_Medina
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spelling paper:paper_19450494_v3E_n3_p1042_Medina2023-06-08T16:32:28Z Role of histamine H4 receptor in breast cancer cell proliferation Apoptosis Cell Senescence Histamine H4 Receptor Human Breast Cancer Proliferation 1 (5 chloro 2 indolylcarbonyl) 4 methylpiperazine 1 [2 (amidinothio)ethyl]guanidine clobenpropit cyclic AMP histamine histamine H3 receptor antagonist histamine H4 receptor lipocortin 5 unclassified drug G protein coupled receptor histamine receptor HRH4 protein, human primer DNA apoptosis article breast cancer cancer cell culture cell aging cell proliferation controlled study human human cell nick end labeling protein expression signal transduction breast tumor female nucleotide sequence pathology physiology reverse transcription polymerase chain reaction tumor cell line Western blotting Apoptosis Base Sequence Blotting, Western Breast Neoplasms Cell Line, Tumor Cell Proliferation DNA Primers Female Humans In Situ Nick-End Labeling Receptors, G-Protein-Coupled Receptors, Histamine Reverse Transcriptase Polymerase Chain Reaction In order to better understand the role of histamine H4 (H4R) receptor in breast cancer, we studied the receptor expression pattern, associated signal transduction pathway and biological responses, in breast cancer cell lines with different malignant characteristics. A different pattern of protein expression was observed in MDA-MB-231 compared to MCF-7 cells determined by western blot, exhibiting the presence of a diverse range of molecular weight species of the H4R. H4R agonist reduced cyclic adenosine monophosphate (cAMP) formation induced by forskolin only in MCF-7 cells. In MDA-MB-231 cells, H4R agonists significantly decreased cell roliferation, augmented the Annexin-V and TdT-mediated UTP-biotin Nick End labelling (TUNEL) positive cells and produced a 2.5-fold increase in cell senescence. In MCF-7 cells, H4R agonists inhibited proliferation by 50%, increasing the exponential doubling time. This effect was associated to an augment in Annexin-V and TUNEL positive cells, and a 2-fold increase in cell senescence. We conclude that H4R is functionally expressed in human breast cancer cell lines, exhibiting a key role in histaminemediated biological processes such as cell proliferation, senescence and apoptosis. 2011 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19450494_v3E_n3_p1042_Medina http://hdl.handle.net/20.500.12110/paper_19450494_v3E_n3_p1042_Medina
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Apoptosis
Cell Senescence
Histamine H4 Receptor
Human Breast Cancer
Proliferation
1 (5 chloro 2 indolylcarbonyl) 4 methylpiperazine
1 [2 (amidinothio)ethyl]guanidine
clobenpropit
cyclic AMP
histamine
histamine H3 receptor antagonist
histamine H4 receptor
lipocortin 5
unclassified drug
G protein coupled receptor
histamine receptor
HRH4 protein, human
primer DNA
apoptosis
article
breast cancer
cancer cell culture
cell aging
cell proliferation
controlled study
human
human cell
nick end labeling
protein expression
signal transduction
breast tumor
female
nucleotide sequence
pathology
physiology
reverse transcription polymerase chain reaction
tumor cell line
Western blotting
Apoptosis
Base Sequence
Blotting, Western
Breast Neoplasms
Cell Line, Tumor
Cell Proliferation
DNA Primers
Female
Humans
In Situ Nick-End Labeling
Receptors, G-Protein-Coupled
Receptors, Histamine
Reverse Transcriptase Polymerase Chain Reaction
spellingShingle Apoptosis
Cell Senescence
Histamine H4 Receptor
Human Breast Cancer
Proliferation
1 (5 chloro 2 indolylcarbonyl) 4 methylpiperazine
1 [2 (amidinothio)ethyl]guanidine
clobenpropit
cyclic AMP
histamine
histamine H3 receptor antagonist
histamine H4 receptor
lipocortin 5
unclassified drug
G protein coupled receptor
histamine receptor
HRH4 protein, human
primer DNA
apoptosis
article
breast cancer
cancer cell culture
cell aging
cell proliferation
controlled study
human
human cell
nick end labeling
protein expression
signal transduction
breast tumor
female
nucleotide sequence
pathology
physiology
reverse transcription polymerase chain reaction
tumor cell line
Western blotting
Apoptosis
Base Sequence
Blotting, Western
Breast Neoplasms
Cell Line, Tumor
Cell Proliferation
DNA Primers
Female
Humans
In Situ Nick-End Labeling
Receptors, G-Protein-Coupled
Receptors, Histamine
Reverse Transcriptase Polymerase Chain Reaction
Role of histamine H4 receptor in breast cancer cell proliferation
topic_facet Apoptosis
Cell Senescence
Histamine H4 Receptor
Human Breast Cancer
Proliferation
1 (5 chloro 2 indolylcarbonyl) 4 methylpiperazine
1 [2 (amidinothio)ethyl]guanidine
clobenpropit
cyclic AMP
histamine
histamine H3 receptor antagonist
histamine H4 receptor
lipocortin 5
unclassified drug
G protein coupled receptor
histamine receptor
HRH4 protein, human
primer DNA
apoptosis
article
breast cancer
cancer cell culture
cell aging
cell proliferation
controlled study
human
human cell
nick end labeling
protein expression
signal transduction
breast tumor
female
nucleotide sequence
pathology
physiology
reverse transcription polymerase chain reaction
tumor cell line
Western blotting
Apoptosis
Base Sequence
Blotting, Western
Breast Neoplasms
Cell Line, Tumor
Cell Proliferation
DNA Primers
Female
Humans
In Situ Nick-End Labeling
Receptors, G-Protein-Coupled
Receptors, Histamine
Reverse Transcriptase Polymerase Chain Reaction
description In order to better understand the role of histamine H4 (H4R) receptor in breast cancer, we studied the receptor expression pattern, associated signal transduction pathway and biological responses, in breast cancer cell lines with different malignant characteristics. A different pattern of protein expression was observed in MDA-MB-231 compared to MCF-7 cells determined by western blot, exhibiting the presence of a diverse range of molecular weight species of the H4R. H4R agonist reduced cyclic adenosine monophosphate (cAMP) formation induced by forskolin only in MCF-7 cells. In MDA-MB-231 cells, H4R agonists significantly decreased cell roliferation, augmented the Annexin-V and TdT-mediated UTP-biotin Nick End labelling (TUNEL) positive cells and produced a 2.5-fold increase in cell senescence. In MCF-7 cells, H4R agonists inhibited proliferation by 50%, increasing the exponential doubling time. This effect was associated to an augment in Annexin-V and TUNEL positive cells, and a 2-fold increase in cell senescence. We conclude that H4R is functionally expressed in human breast cancer cell lines, exhibiting a key role in histaminemediated biological processes such as cell proliferation, senescence and apoptosis.
title Role of histamine H4 receptor in breast cancer cell proliferation
title_short Role of histamine H4 receptor in breast cancer cell proliferation
title_full Role of histamine H4 receptor in breast cancer cell proliferation
title_fullStr Role of histamine H4 receptor in breast cancer cell proliferation
title_full_unstemmed Role of histamine H4 receptor in breast cancer cell proliferation
title_sort role of histamine h4 receptor in breast cancer cell proliferation
publishDate 2011
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19450494_v3E_n3_p1042_Medina
http://hdl.handle.net/20.500.12110/paper_19450494_v3E_n3_p1042_Medina
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