{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Rymuza J"],"funding":["Maria Sklodowska-Curie National Research Institute of Oncology"],"pagination":["3846"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9738119"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["11(23)"],"pubmed_abstract":["Acromegaly results from growth hormone hypersecretion, predominantly caused by a somatotroph pituitary neuroendocrine tumor (PitNET). Acromegaly-causing tumors are histologically diverse. Our aim was to determine transcriptomic profiles of various somatotroph PitNETs and to evaluate clinical implication of differential gene expression. A total of 48 tumors were subjected to RNA sequencing, while expression of selected genes was assessed in 134 tumors with qRT-PCR. Whole-transcriptome analysis revealed three transcriptomic groups of somatotroph PitNETs. They differ in expression of numerous genes including those involved in growth hormone secretion and known prognostic genes. Transcriptomic subgroups can be distinguished by determining the expression of marker genes. Analysis of the entire cohort of patients confirmed differences between molecular subtypes of tumors. Transcriptomic group 1 includes ~20% of acromegaly patients with <i>GNAS</i> mutations-negative, mainly densely granulated tumors that co-express <i>GIPR</i> and <i>NR5A1</i> (SF-1). SF-1 expression was verified with immunohistochemistry. Transcriptomic group 2 tumors are the most common (46%) and include mainly <i>GNAS</i>-mutated, densely granulated somatotroph and mixed PitNETs. They have a smaller size and express favorable prognosis-related genes. Transcriptomic group 3 includes predominantly sparsely granulated somatotroph PitNETs with low <i>GNAS</i> mutations frequency causing ~35% of acromegaly. Ghrelin signaling is implicated in their pathogenesis. They have an unfavorable gene expression profile and higher invasive growth rate."],"journal":["Cells"],"pubmed_title":["Transcriptomic Classification of Pituitary Neuroendocrine Tumors Causing Acromegaly."],"pmcid":["PMC9738119"],"funding_grant_id":["SN/GW04/2020"],"pubmed_authors":["Mossakowska BJ","Baluszek S","Zielinski G","Bujko M","Kunicki J","Maksymowicz M","Kober P","Rusetska N","Nyc A","Rymuza J"],"additional_accession":[]},"is_claimable":false,"name":"Transcriptomic Classification of Pituitary Neuroendocrine Tumors Causing Acromegaly.","description":"Acromegaly results from growth hormone hypersecretion, predominantly caused by a somatotroph pituitary neuroendocrine tumor (PitNET). Acromegaly-causing tumors are histologically diverse. Our aim was to determine transcriptomic profiles of various somatotroph PitNETs and to evaluate clinical implication of differential gene expression. A total of 48 tumors were subjected to RNA sequencing, while expression of selected genes was assessed in 134 tumors with qRT-PCR. Whole-transcriptome analysis revealed three transcriptomic groups of somatotroph PitNETs. They differ in expression of numerous genes including those involved in growth hormone secretion and known prognostic genes. Transcriptomic subgroups can be distinguished by determining the expression of marker genes. Analysis of the entire cohort of patients confirmed differences between molecular subtypes of tumors. Transcriptomic group 1 includes ~20% of acromegaly patients with <i>GNAS</i> mutations-negative, mainly densely granulated tumors that co-express <i>GIPR</i> and <i>NR5A1</i> (SF-1). SF-1 expression was verified with immunohistochemistry. Transcriptomic group 2 tumors are the most common (46%) and include mainly <i>GNAS</i>-mutated, densely granulated somatotroph and mixed PitNETs. They have a smaller size and express favorable prognosis-related genes. Transcriptomic group 3 includes predominantly sparsely granulated somatotroph PitNETs with low <i>GNAS</i> mutations frequency causing ~35% of acromegaly. Ghrelin signaling is implicated in their pathogenesis. They have an unfavorable gene expression profile and higher invasive growth rate.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Nov","modification":"2025-04-22T05:41:13.942Z","creation":"2025-04-05T21:26:00.55Z"},"accession":"S-EPMC9738119","cross_references":{"pubmed":["36497102"],"doi":["10.3390/cells11233846"]}}