miRNA Expression Profiling in G1 and G2 Pancreatic Neuroendocrine Tumors DOI Open Access
Gábor Nyírő, Balint Szeredas, Ábel Decmann

et al.

Cancers, Journal Year: 2024, Volume and Issue: 16(14), P. 2528 - 2528

Published: July 13, 2024

Pancreatic neuroendocrine neoplasms pose a growing clinical challenge due to their rising incidence and variable prognosis. The current study aims investigate microRNAs (miRNA; miR) as potential biomarkers for distinguishing between grade 1 (G1) 2 (G2) pancreatic tumors (PanNET). A total of 33 formalin-fixed, paraffin-embedded samples were analyzed, comprising 17 G1 16 G2 tumors. Initially, literature-based miRNAs validated via real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR), confirming significant downregulation

Language: Английский

Sarcopenia in Patients with Advanced Gastrointestinal Well-Differentiated Neuroendocrine Tumors DOI Open Access
Elena Romano, Michela Polici, Matteo Marasco

et al.

Nutrients, Journal Year: 2024, Volume and Issue: 16(14), P. 2224 - 2224

Published: July 11, 2024

Background: Neuroendocrine neoplasms (NENs) are slow-growing tumors. Sarcopenia is defined as the loss of muscle mass, strength, and physical performance. First-line NEN therapy somatostatin analogs, which could be responsible for malabsorption conditions, such pancreatic exocrine insufficiency (EPI) with underlying sarcopenia. Aim: Evaluate prevalence sarcopenia in patients NENs at diagnosis during follow-up. Methods: A retrospective single-center study was conducted, including advanced intestinal G1/G2 (excluded NENs). CT scans were analyzed after 6 months therapy, skeletal index assessed. Results: total 30 (F:M = 6:24) enrolled, following primary tumor sites: 25 ileum, 1 stomach, 2 jejunum, duodenum. At diagnosis, 20 (66.6%) showed sarcopenic SMI values, 10 (33.3%) non-sarcopenic values. follow-up, three more developed Statistical significance relation to presence found group carcinoid syndrome (p 0.0178), EPI 0.0018), weight 0.0001). Conclusion: present 2/3 It reasonable consider this condition improve clinical outcomes.

Language: Английский

Citations

4

Gastroenteropancreatic neuroendocrine neoplasms: epidemiology, genetics, and treatment DOI Creative Commons

Baizhou Tan,

Beiyu Zhang,

Hongping Chen

et al.

Frontiers in Endocrinology, Journal Year: 2024, Volume and Issue: 15

Published: Sept. 30, 2024

The incidence of gastroenteropancreatic neuroendocrine neoplasms (GEP NEN) is increasing at a rapid pace and becoming an increasingly important consideration in clinical care. Epidemiological data from multiple countries indicate that the exhibits regional, site-specific, gender-based variations. While genetics pathogenesis some GEP NEN, particularly pancreatic NENs, have been investigated, there are still many mechanisms require further investigation. management NEN diverse, but surgery remains primary option for most cases. Peptide receptor radionuclide therapy (PRRT) effective treatment, several trials exploring potential immunotherapy targeted therapy, as well combination therapy.

Language: Английский

Citations

4

The current status of somatostatin analogs in the treatment of neuroendocrine tumors and future perspectives DOI
E Lauricella,

Sofija Vilisova,

Nada Chaoul

et al.

Expert Review of Neurotherapeutics, Journal Year: 2024, Volume and Issue: unknown, P. 1 - 14

Published: Oct. 16, 2024

Somatostatin analogs (SSAs) were developed as antisecretory agents to palliate hormonal symptoms in patients with functioning neuroendocrine tumors (NETs). Their antiproliferative activity has been established the phase 3 PROMID and CLARINET trials. SSAs currently represent standard first-line therapy for majority of well-differentiated G1/G2 gastroenteropancreatic NETs well pulmonary NETs.

Language: Английский

Citations

1

Exploring Carcinoid Syndrome in Neuroendocrine Tumors: Insights from a Multidisciplinary Narrative Review DOI Open Access
Matteo Marasco, Elena Romano, Giulia Arrivi

et al.

Cancers, Journal Year: 2024, Volume and Issue: 16(22), P. 3831 - 3831

Published: Nov. 14, 2024

Carcinoid syndrome (CS) is a rare condition associated with neuroendocrine tumors (NETs), particularly those originating in the gastrointestinal tract, which secrete bioactive substances like serotonin. The management of CS requires multidisciplinary approach due to its complex clinical manifestations, including flushing, diarrhea, bronchospasm, and carcinoid heart disease. Optimal care involves collaboration between several professional figures oncologists, endocrinologists, gastroenterologists, surgeons, dietitians. Currently, wide range treatments are available, focused on both symptom control tumor burden reduction. Somatostatin analogs (SSAs) first-line therapy for relief. Still, patients progressive disease or refractory CS, other options include targeted therapies, peptide receptor radionuclide (PRRT), liver-directed surgical resection, when feasible. Furthermore, complications related prolonged serotonin release malnutrition as result exocrine pancreatic insufficiency, post-surgical conditions, vitamin deficit, chronic diarrhea often early detection mitigate symptoms improve quality life these patients. complexity necessitates individualized continuous coordination among specialists optimize outcomes enhance patient well-being.

Language: Английский

Citations

1

miRNA Expression Profiling in G1 and G2 Pancreatic Neuroendocrine Tumors DOI Open Access
Gábor Nyírő, Balint Szeredas, Ábel Decmann

et al.

Cancers, Journal Year: 2024, Volume and Issue: 16(14), P. 2528 - 2528

Published: July 13, 2024

Pancreatic neuroendocrine neoplasms pose a growing clinical challenge due to their rising incidence and variable prognosis. The current study aims investigate microRNAs (miRNA; miR) as potential biomarkers for distinguishing between grade 1 (G1) 2 (G2) pancreatic tumors (PanNET). A total of 33 formalin-fixed, paraffin-embedded samples were analyzed, comprising 17 G1 16 G2 tumors. Initially, literature-based miRNAs validated via real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR), confirming significant downregulation

Language: Английский

Citations

0