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ProteomicsLC-MS of Human Blood of Pancreatic neuroendocrine tumors
Pancreatic Neuroendocrine tumors are challenging to diagnose and often detected at advanced stages due to lack of specific and sensitive biomarkers. This study utilized proteomics as a valuable approach for cancer biomarker discovery, therefore, mass spectrometry-based proteomic profiling was conduc...
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD045045 | Pride
Human Pancreatic neuroendocrine tumors Lc-ms Plasma 
TranscriptomicsGene expression profiles of thymic neuroendocrine tumors (carcinoids) with ectopic ACTH syndrome
Although there has been increased knowledge about the molecular biology of neuroendocrine tumors (NETs), little is known about thymic carcinoids and even less about those with excessive hormone disorders, such as ectopic ACTH syndrome. This study was designed to gain insights into molecular networks...
ORGANISM(S): Homo sapiens 
2009-08-13 | E-GEOD-17619 | biostudies-arrayexpress
ProteomicsProteogenomic characterization of pancreatic neuroendocrine tumor
To characterize pancreatic neuroendocrine tumor at protein level, we performed mass spectromery-based proteome analysis using clinical FFPE tissue samples.
ORGANISM(S): Homo sapiens (Human) 
2024-07-10 | PXD034571 | Pride
Human Tissue Pancreatic neuroendocrine tumor 
ProteomicsPeptidomic analysis of pancreatic neurodendocrine tumours (Glucagonoma)
A peptidomic analysis of plasma from patients with well characterised pancreatic neuroendocrine tumours (PNET) was performed. A nano LC-MS analysis identified a number of peptides from the glucagon gene, which were idenfiried in a previous case study using multiple immunoassays. Peptides to other pr...
ORGANISM(S): Homo Sapiens (ncbitaxon:9606) 
2018-08-31 | MSV000082880 | MassIVE
GenomicWhole Exome Sequencing of Pancreatic Neuroendocrine Tumors

Pancreatic neuroendocrine tumors (PNETs), often referred to as "islet cell tumors", are neuroendocrine neoplasms that arise from cells of the endocrine and nervous system within the pancreas. These rare tumors which originate from the pancreatic islet are divided into many categories and are ofte...

phs000871 | dbGaP
GenomicEnhancer Signatures of Neuroendocrine Tumors

Most pancreatic neuroendocrine tumors (PNETs) do not produce symptoms of hormonal excess and are hence considered “non-functional”. Their clinical behaviors vary widely, emphasizing the need for a robust classification with prognostic power. Using enhancer maps to infer regulatory pro...

phs001910 | dbGaP
TranscriptomicsGenome-wide methylation profiling of sporadic Pancreatic Neuroendocrine Tumors
Pancreatic neuroendocrine tumors (PanNETs) account for 1-3% of all neoplasms of the pancreas. Epigenetic changes seem to be the main drivers of PanNET tumorigenesis. Indeed, the most frequent mutated genes in PanNETs are DAXX (Death domain associated protein 6), ATRX (Transcriptional Regulator ATRX)...
ORGANISM(S): Homo sapiens 
2022-11-30 | E-MTAB-11962 | biostudies-arrayexpress
TranscriptomicsGenome-wide methylation profiling of sporadic Pancreatic Neuroendocrine Tumors
Pancreatic neuroendocrine tumors (PanNETs) account for 1-3% of all neoplasms of the pancreas. Epigenetic changes seem to be the main drivers of PanNET tumorigenesis. Indeed, the most frequent mutated genes in PanNETs are DAXX (Death domain associated protein 6), ATRX (Transcriptional Regulator ATRX)...
ORGANISM(S): Homo sapiens 
2022-11-30 | E-MTAB-11965 | biostudies-arrayexpress
TranscriptomicsGenome-wide methylation profiling of sporadic Pancreatic Neuroendocrine Tumors
Pancreatic neuroendocrine tumors (PanNETs) account for 1-3% of all neoplasms of the pancreas. Epigenetic changes seem to be the main drivers of PanNET tumorigenesis. Indeed, the most frequent mutated genes in PanNETs are DAXX (Death domain associated protein 6), ATRX (Transcriptional Regulator ATRX)...
ORGANISM(S): Homo sapiens 
2020-11-30 | E-MTAB-7924 | biostudies-arrayexpress
UnknownEverolimus for advanced pancreatic neuroendocrine tumors.
Not available
S-EPMC4208619 | biostudies-literature
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