New Mouse Model Suggests That Some Neuroendocrine Tumors May Originate From Neural Crest-Derived Cells
- PMID: 36084750
- PMCID: PMC9606794
- DOI: 10.1016/j.jcmgh.2022.08.005
New Mouse Model Suggests That Some Neuroendocrine Tumors May Originate From Neural Crest-Derived Cells
Comment on
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GFAP-directed Inactivation of Men1 Exploits Glial Cell Plasticity in Favor of Neuroendocrine Reprogramming.Cell Mol Gastroenterol Hepatol. 2022;14(5):1025-1051. doi: 10.1016/j.jcmgh.2022.06.009. Epub 2022 Jul 11. Cell Mol Gastroenterol Hepatol. 2022. PMID: 35835391 Free PMC article.
References
-
- Cives M., Strosberg J.R. Gastroenteropancreatic neuroendocrine tumors. CA Cancer J Clin. 2018;68:471–487. - PubMed
-
- Thakker R.V., Newey P.J., Walls G.V., Bilezikian J., Dralle H., Ebeling P.R., Melmed S., Sakurai A., Tonelli F., Brandi M.L., Endocrine S. Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1) J Clin Endocrinol Metab. 2012;97:2990–3011. - PubMed
-
- Jiao Y., Shi C., Edil B.H., de Wilde R.F., Klimstra D.S., Maitra A., Schulick R.D., Tang L.H., Wolfgang C.L., Choti M.A., Velculescu V.E., Diaz L.A., Jr., Vogelstein B., Kinzler K.W., Hruban R.H., Papadopoulos N. DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors. Science. 2011;331:1199–1203. - PMC - PubMed
-
- Crabtree J.S., Scacheri P.C., Ward J.M., Garrett-Beal L., Emmert-Buck M.R., Edgemon K.A., Lorang D., Libutti S.K., Chandrasekharappa S.C., Marx S.J., Spiegel A.M., Collins F.S. A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors. Proc Natl Acad Sci U S A. 2001;98:1118–1123. - PMC - PubMed
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