Expression of Growth Hormone-Releasing Hormone and Its Receptor Splice Variants in a Cohort of Hungarian Pediatric Patients with Hematological and Oncological Disorders: A Pilot Study.
Éva JuhászZsuzsanna SzabóAndrew V SchallyJózsef KirályPetra FodorGábor KónyaBalázs DezsőErzsébet SzabóGábor HalmosCsongor KissPublished in: International journal of molecular sciences (2024)
Hematological and oncological diseases are still among the leading causes of childhood mortality. Expression of growth hormone-releasing hormone (GHRH) and its receptors (GHRH-R) has been previously demonstrated in various human tumors, but very limited findings are available about the presence and potential function of GHRH-Rs in oncological and hematological disorders of children. In this study, we aimed to investigate the expression of mRNA for GHRH and splice variant 1 (SV) of GHRH-R in 15 pediatric hematological/oncological specimens by RT-PCR. The presence and binding characteristics of GHRH-R protein were also studied by Western blot and ligand competition assays. Of the fifteen specimens studied, eleven pediatric samples (73%) showed the expression of mRNA for GHRH. These eleven samples also expressed mRNA for GHRH receptor SV1. GHRH-R protein was found to be expressed in two benign tumor samples and five malignant tumors examined by Western blot. The presence of specific, high affinity binding sites on GHRH-R was demonstrated in all of the seven human pediatric solid tumor samples investigated. Our results show that the expression of GHRH and SV1 of GHRH-R in hemato-oncological diseases in children can pave the way for further investigation of GHRH-Rs as potential molecular targets for diagnosis and therapy.
Keyphrases
- binding protein
- poor prognosis
- growth hormone
- rectal cancer
- endothelial cells
- radical prostatectomy
- young adults
- prostate cancer
- robot assisted
- cardiovascular disease
- south africa
- gene expression
- cardiovascular events
- long non coding rna
- stem cells
- copy number
- high throughput
- risk assessment
- mass spectrometry
- genome wide
- transcription factor
- bone marrow
- protein protein
- single cell
- mesenchymal stem cells
- atomic force microscopy