Herrera-Martínez, A. D. et al. Neuroendocrine neoplasms: current and potential diagnostic, predictive and prognostic markers. Endocr. Relat. Cancer 26, R157–R179 (2019).
Smolkova, B. et al. Liquid biopsy and preclinical tools for advancing diagnosis and treatment of patients with pancreatic neuroendocrine neoplasms. Crit. Rev. Oncol. Hematol. 180, 103865 (2022).
Fassnacht, M. et al. Adrenocortical carcinomas and malignant phaeochromocytomas: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 31, 1476–1490 (2020).
Article CAS PubMed Google Scholar
Russano, M. et al. Liquid biopsy and tumor heterogeneity in metastatic solid tumors: the potentiality of blood samples. J. Exp. Clin. Cancer Res. 39, 95 (2020).
Article CAS PubMed PubMed Central Google Scholar
Asa, S. L. & Mete, O. Endocrine pathology: past, present and future. Pathology 50, 111–118 (2018).
Rindi, G. et al. Overview of the 2022 WHO classification of neuroendocrine neoplasms. Endocr. Pathol. 33, 115–154 (2022). A comprehensive review on the current classification of NETs.
Article CAS PubMed Google Scholar
Asa, S. L., Mete, O., Perry, A. & Osamura, R. Y. Overview of the 2022 WHO classification of pituitary tumors. Endocr. Pathol. 33, 6–26 (2022). A recent review on the current classification of pituitary tumours.
Article CAS PubMed Google Scholar
Yeh, M. W. et al. Incidence and prevalence of primary hyperparathyroidism in a racially mixed population. J. Clin. Endocrinol. Metab. 98, 1122–1129 (2013).
Article CAS PubMed PubMed Central Google Scholar
Minisola, S. et al. Epidemiology, pathophysiology, and genetics of primary hyperparathyroidism. J. Bone Miner. Res. 37, 2315–2329 (2022).
Daly, A. F. & Beckers, A. The epidemiology of pituitary adenomas. Endocrinol. Metab. Clin. North Am. 49, 347–355 (2020).
Dasari, A. et al. Trends in the incidence, prevalence, and survival outcomes in patients with neuroendocrine tumors in the United States. JAMA Oncol. 3, 1335–1342 (2017).
Article PubMed PubMed Central Google Scholar
Heaphy C. M. & Singhi A. D. The diagnostic and prognostic utility of incorporating DAXX, ATRX, and alternative lengthening of telomeres (ALT) to the evaluation of pancreatic neuroendocrine tumors (PanNETs). Hum. Pathol. 129, 11–20 (2022).
Article CAS PubMed Google Scholar
Berends, A. M. A. et al. Incidence of pheochromocytoma and sympathetic paraganglioma in the Netherlands: a nationwide study and systematic review. Eur. J. Int. Med. 51, 68–73 (2018).
Lenders, J. W. M. et al. Genetics, diagnosis, management and future directions of research of phaeochromocytoma and paraganglioma: a position statement and consensus of the Working Group on Endocrine Hypertension of the European Society of Hypertension. J. Hypertens. 38, 1443–1456 (2020).
Article CAS PubMed PubMed Central Google Scholar
Bancos, I. & Prete, A. Approach to the patient with adrenal incidentaloma. J. Clin. Endocrinol. Metab. 106, 3331–3353 (2021).
Article PubMed PubMed Central Google Scholar
Angelousi, A. et al. Molecular targeted therapies in adrenal, pituitary and parathyroid malignancies. Endocr. Relat. Cancer 24, R239–R259 (2017).
Fishbein, L. et al. Comprehensive molecular characterization of pheochromocytoma and paraganglioma. Cancer Cell 31, 181–193 (2017). A ground-breaking study on the molecular features of PPGL.
Article CAS PubMed PubMed Central Google Scholar
Marini, F. et al. Genetics and epigenetics of parathyroid carcinoma. Front. Endocrinol. 13, 834362 (2022).
Gaujoux, S. et al. Wnt/beta-catenin and 3′,5′-cyclic adenosine 5′-monophosphate/protein kinase A signaling pathways alterations and somatic beta-catenin gene mutations in the progression of adrenocortical tumors. J. Clin. Endocrinol. Metab. 93, 4135–4140 (2008).
Article CAS PubMed Google Scholar
Nosé, V., Gill, A., Teijeiro, J. M. C., Perren, A. & Erickson, L. Overview of the 2022 WHO classification of familial endocrine tumor syndromes. Endocr. Pathol. 33, 197–227 (2022).
Brandi, M. L. et al. Multiple endocrine neoplasia type 1: latest insights. Endocr. Rev. 42, 133–170 (2021).
Ruggeri, R. M. et al. Multiple endocrine neoplasia type 4 (MEN4): a thorough update on the latest and least known MEN syndrome. Endocrine 82, 480–490 (2023).
Article CAS PubMed Google Scholar
Minnetti, M. & Grossman, A. Somatic and germline mutations in NETs: implications for their diagnosis and management. Best Pract. Res. Clin. Endocrinol. Metab. 30, 115–127 (2016).
Article CAS PubMed Google Scholar
MacFarlane, J. et al. A review of the tumour spectrum of germline succinate dehydrogenase gene mutations: beyond phaeochromocytoma and paraganglioma. Clin. Endocrinol. 93, 528–538 (2020).
Huang, J. et al. The same pocket in menin binds both MLL and JUND but has opposite effects on transcription. Nature 482, 542–546 (2012).
Article CAS PubMed PubMed Central Google Scholar
Matkar, S., Thiel, A. & Hua, X. Menin: a scaffold protein that controls gene expression and cell signaling. Trends Biochem. Sci. 38, 394–402 (2013).
Article CAS PubMed PubMed Central Google Scholar
Kaji, H., Canaff, L., Lebrun, J. J., Goltzman, D. & Hendy, G. N. Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling. Proc. Natl Acad. Sci. USA 98, 3837–3842 (2001).
Article CAS PubMed PubMed Central Google Scholar
Wong, C. et al. Two well-differentiated pancreatic neuroendocrine tumor mouse models. Cell Death Diff. 27, 269–283 (2020).
Luo, J., Manning, B. D. & Cantley, L. C. Targeting the PI3K-Akt pathway in human cancer: rationale and promise. Cancer Cell. 4, 257–262 (2003).
Article CAS PubMed Google Scholar
Segouffin-Cariou, C. & Billaud, M. Transforming ability of MEN2A-RET requires activation of the phosphatidylinositol 3-kinase/AKT signaling pathway. J. Biol. Chem. 275, 3568–3576 (2000).
Article CAS PubMed Google Scholar
Anastasaki, C., Orozco, P. & Gutmann, D. H. RAS and beyond: the many faces of the neurofibromatosis type 1 protein. Dis. Mod. Mech. 15, dmm049362 (2022).
Adhikary, S. & Eilers, M. Transcriptional regulation and transformation by Myc proteins. Nat. Rev. Mol. Cell Biol. 6, 635–645 (2005).
Article CAS PubMed Google Scholar
Augert, A. et al. MAX functions as a tumor suppressor and rewires metabolism in small cell lung cancer. Cancer Cell 38, 97–114.e117 (2020).
留言 (0)