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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Autor principal: Medina, V.A
Otros Autores: Brenzoni, P.G, Lamas, D.J.M, Massari, N., Mondillo, C., Nunez, M.A, Pignataro, O., Rivera, E.S
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2011
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Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a clobenpropit, 145231-45-4; cyclic AMP, 60-92-4; histamine, 51-45-6, 56-92-8, 93443-21-1; histamine H4 receptor, 272100-58-0; lipocortin 5, 111237-10-6; DNA Primers; HRH4 protein, human; Receptors, G-Protein-Coupled; Receptors, Histamine 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
100 1 |a Medina, V.A. 
245 1 0 |a Role of histamine H4 receptor in breast cancer cell proliferation 
260 |c 2011 
270 1 0 |m Rivera, E.S.; Laboratory of Radioisotopes, School of Pharmacy and Biochemistry, University of Buenos Aires, Junin 956, Buenos Aires, 1113, Argentina; email: erivera@ffyb.uba.ar 
506 |2 openaire  |e Política editorial 
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520 3 |a 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.  |l eng 
593 |a Laboratory of Radioisotopes, School of Pharmacy and Biochemistry, University of Buenos Aires, Junin 956, Buenos Aires, 1113, Argentina 
593 |a National Scientific and Technical Research Council (Conicet), Buenos Aires, Argentina 
593 |a Laboratory of Molecular Endocrinology and Signal Transduction, Institute of Biology and Experimental Medicine-Conicet, Buenos Aires, 1428, Argentina 
690 1 0 |a APOPTOSIS 
690 1 0 |a CELL SENESCENCE 
690 1 0 |a HISTAMINE H4 RECEPTOR 
690 1 0 |a HUMAN BREAST CANCER 
690 1 0 |a PROLIFERATION 
690 1 0 |a 1 (5 CHLORO 2 INDOLYLCARBONYL) 4 METHYLPIPERAZINE 
690 1 0 |a 1 [2 (AMIDINOTHIO)ETHYL]GUANIDINE 
690 1 0 |a CLOBENPROPIT 
690 1 0 |a CYCLIC AMP 
690 1 0 |a HISTAMINE 
690 1 0 |a HISTAMINE H3 RECEPTOR ANTAGONIST 
690 1 0 |a HISTAMINE H4 RECEPTOR 
690 1 0 |a LIPOCORTIN 5 
690 1 0 |a UNCLASSIFIED DRUG 
690 1 0 |a G PROTEIN COUPLED RECEPTOR 
690 1 0 |a HISTAMINE RECEPTOR 
690 1 0 |a HRH4 PROTEIN, HUMAN 
690 1 0 |a PRIMER DNA 
690 1 0 |a APOPTOSIS 
690 1 0 |a ARTICLE 
690 1 0 |a BREAST CANCER 
690 1 0 |a CANCER CELL CULTURE 
690 1 0 |a CELL AGING 
690 1 0 |a CELL PROLIFERATION 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a HUMAN 
690 1 0 |a HUMAN CELL 
690 1 0 |a NICK END LABELING 
690 1 0 |a PROTEIN EXPRESSION 
690 1 0 |a SIGNAL TRANSDUCTION 
690 1 0 |a BREAST TUMOR 
690 1 0 |a FEMALE 
690 1 0 |a NUCLEOTIDE SEQUENCE 
690 1 0 |a PATHOLOGY 
690 1 0 |a PHYSIOLOGY 
690 1 0 |a REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION 
690 1 0 |a TUMOR CELL LINE 
690 1 0 |a WESTERN BLOTTING 
690 1 0 |a APOPTOSIS 
690 1 0 |a BASE SEQUENCE 
690 1 0 |a BLOTTING, WESTERN 
690 1 0 |a BREAST NEOPLASMS 
690 1 0 |a CELL LINE, TUMOR 
690 1 0 |a CELL PROLIFERATION 
690 1 0 |a DNA PRIMERS 
690 1 0 |a FEMALE 
690 1 0 |a HUMANS 
690 1 0 |a IN SITU NICK-END LABELING 
690 1 0 |a RECEPTORS, G-PROTEIN-COUPLED 
690 1 0 |a RECEPTORS, HISTAMINE 
690 1 0 |a REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION 
653 0 0 |a jnj 7777120; vuf 8430 
700 1 |a Brenzoni, P.G. 
700 1 |a Lamas, D.J.M. 
700 1 |a Massari, N. 
700 1 |a Mondillo, C. 
700 1 |a Nunez, M.A. 
700 1 |a Pignataro, O. 
700 1 |a Rivera, E.S. 
773 0 |d 2011  |g v. 3 E  |h pp. 1042-1060  |k n. 3  |p Front. Biosci. Elite  |x 19450494  |t Frontiers in Bioscience - Elite 
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