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Thoracic and duodenopancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1: natural history and function of menin in tumorigenesis.
Endocr Relat Cancer. 2014 Jun; 21(3):R121-42.ER

Abstract

Mutations of the multiple endocrine neoplasia type 1 (MEN1) gene lead to loss of function of its protein product menin. In keeping with its tumor suppressor function in endocrine tissues, the majority of the MEN1-related neuroendocrine tumors (NETs) show loss of heterozygosity (LOH) on chromosome 11q13. In sporadic NETs, MEN1 mutations and LOH are also reported, indicating common pathways in tumor development. Prevalence of thymic NETs (thNETs) and pulmonary carcinoids in MEN1 patients is 2-8%. Pulmonary carcinoids may be underreported and research on natural history is limited, but disease-related mortality is low. thNETs have a high mortality rate. Duodenopancreatic NETs (dpNETs) are multiple, almost universally found at pathology, and associated with precursor lesions. Gastrinomas are usually located in the duodenal submucosa while other dpNETs are predominantly pancreatic. dpNETs are an important determinant of MEN1-related survival, with an estimated 10-year survival of 75%. Survival differs between subtypes and apart from tumor size there are no known prognostic factors. Natural history of nonfunctioning pancreatic NETs needs to be redefined because of increased detection of small tumors. MEN1-related gastrinomas seem to behave similar to their sporadic counterparts, while insulinomas seem to be more aggressive. Investigations into the molecular functions of menin have led to new insights into MEN1-related tumorigenesis. Menin is involved in gene transcription, both as an activator and repressor. It is part of chromatin-modifying protein complexes, indicating involvement of epigenetic pathways in MEN1-related NET development. Future basic and translational research aimed at NETs in large unbiased cohorts will clarify the role of menin in NET tumorigenesis and might lead to new therapeutic options.

Authors+Show Affiliations

Division of Internal Medicine and Dermatology, Department of Internal Medicine, University Medical Center Utrecht, Internal post number L.00.408, PO Box 85500, 3508 GA Utrecht, The Netherlands Division of Biomedical Genetics, Department of Molecular Cancer Research Division of Surgical Specialties, Department of Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Review

Language

eng

PubMed ID

24389729

Citation

Pieterman, C R C., et al. "Thoracic and Duodenopancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1: Natural History and Function of Menin in Tumorigenesis." Endocrine-related Cancer, vol. 21, no. 3, 2014, pp. R121-42.
Pieterman CR, Conemans EB, Dreijerink KM, et al. Thoracic and duodenopancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1: natural history and function of menin in tumorigenesis. Endocr Relat Cancer. 2014;21(3):R121-42.
Pieterman, C. R., Conemans, E. B., Dreijerink, K. M., de Laat, J. M., Timmers, H. T., Vriens, M. R., & Valk, G. D. (2014). Thoracic and duodenopancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1: natural history and function of menin in tumorigenesis. Endocrine-related Cancer, 21(3), R121-42. https://doi.org/10.1530/ERC-13-0482
Pieterman CR, et al. Thoracic and Duodenopancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1: Natural History and Function of Menin in Tumorigenesis. Endocr Relat Cancer. 2014;21(3):R121-42. PubMed PMID: 24389729.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Thoracic and duodenopancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1: natural history and function of menin in tumorigenesis. AU - Pieterman,C R C, AU - Conemans,E B, AU - Dreijerink,K M A, AU - de Laat,J M, AU - Timmers,H Th M, AU - Vriens,M R, AU - Valk,G D, Y1 - 2014/05/06/ PY - 2014/1/7/entrez PY - 2014/1/7/pubmed PY - 2015/1/23/medline KW - MEN1 KW - duodenopancreatic NET KW - epigenetics KW - lung NET KW - menin KW - multiple endocrine neoplasia type 1 KW - natural history KW - neuroendocrine tumors KW - pancreatic NET KW - thymic NET SP - R121 EP - 42 JF - Endocrine-related cancer JO - Endocr Relat Cancer VL - 21 IS - 3 N2 - Mutations of the multiple endocrine neoplasia type 1 (MEN1) gene lead to loss of function of its protein product menin. In keeping with its tumor suppressor function in endocrine tissues, the majority of the MEN1-related neuroendocrine tumors (NETs) show loss of heterozygosity (LOH) on chromosome 11q13. In sporadic NETs, MEN1 mutations and LOH are also reported, indicating common pathways in tumor development. Prevalence of thymic NETs (thNETs) and pulmonary carcinoids in MEN1 patients is 2-8%. Pulmonary carcinoids may be underreported and research on natural history is limited, but disease-related mortality is low. thNETs have a high mortality rate. Duodenopancreatic NETs (dpNETs) are multiple, almost universally found at pathology, and associated with precursor lesions. Gastrinomas are usually located in the duodenal submucosa while other dpNETs are predominantly pancreatic. dpNETs are an important determinant of MEN1-related survival, with an estimated 10-year survival of 75%. Survival differs between subtypes and apart from tumor size there are no known prognostic factors. Natural history of nonfunctioning pancreatic NETs needs to be redefined because of increased detection of small tumors. MEN1-related gastrinomas seem to behave similar to their sporadic counterparts, while insulinomas seem to be more aggressive. Investigations into the molecular functions of menin have led to new insights into MEN1-related tumorigenesis. Menin is involved in gene transcription, both as an activator and repressor. It is part of chromatin-modifying protein complexes, indicating involvement of epigenetic pathways in MEN1-related NET development. Future basic and translational research aimed at NETs in large unbiased cohorts will clarify the role of menin in NET tumorigenesis and might lead to new therapeutic options. SN - 1479-6821 UR - https://www.unboundmedicine.com/medline/citation/24389729/Thoracic_and_duodenopancreatic_neuroendocrine_tumors_in_multiple_endocrine_neoplasia_type_1:_natural_history_and_function_of_menin_in_tumorigenesis_ L2 - https://erc.bioscientifica.com/doi/10.1530/ERC-13-0482 DB - PRIME DP - Unbound Medicine ER -