The DOI matches its Crossref record; 68 of the 68 references it cites were found in a registry or an index.
RET Proto-Oncogene in the Development of Human Cancer
Abstract
The RET proto-oncogene, located on chromosome subband 10q11.2, encodes a receptor tyrosine kinase expressed in tissues and tumors derived from neural crest. Germline (present in every cell of the body) mutations in RET cause multiple endocrine neoplasia type 2 (MEN 2), an inherited cancer syndrome characterized by medullary thyroid carcinoma (MTC), pheochromocytoma (PC), and hyperparathyroidism (HPT). This knowledge has allowed molecular diagnosis and presymptomatic DNA-based testing to become possible. RET testing is considered the standard of care in MEN 2 families because clinical decisions are made based on the results of such gene testing. There appears to be a correlation between specific RET mutation type and organ-specific tumor development. Such knowledge might be useful in tailoring targeted surveillance in the near future. Somatic (in the tumor only) RET mutations have been found in a proportion of sporadic MTCs and PCs. Whether the presence of somatic RET mutation is associated with a poor prognosis is currently being investigated as another tool for molecular medicine.
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Cites
The Protein Kinase Family: Conserved Features and Deduced Phylogeny of the Catalytic Domains
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Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
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Self-citationMutations in the RET proto-oncogene are associated with MEN 2A and FMTC
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Characterization of a multicomponent receptor for GDNF
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Catalytic specificity of protein-tyrosine kinases is critical for selective signalling
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Self-citationActivation of a novel human transforming gene, ret, by DNA rearrangement
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Activation of RET as a Dominant Transforming Gene by Germline Mutations of MEN2A and MEN2B
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Cited by
PTEN: One Gene, Many Syndromes
Eng, C. (2003) · Human Mutation · doi:10.1002/humu.10257 · Cited by 787
Self-citationThe molecular pathogenesis of hereditary and sporadic adrenocortical and adrenomedullary tumors
Koch, C. A., Pacak, K., & Chrousos, G. P. (2002) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2002-021069 · Cited by 177
Koch, C. A., & Sarlis, N. J. (2001) · Journal of Endocrinological Investigation · doi:10.1007/bf03343911 · Cited by 36
Metadata
- Authors
- Eng, C.
- Venue
- Journal of Clinical Oncology
- Published
- 1999-01
- Volume
- 17
- Issue
- 1
- Pages
- 380-380
- ISSN
- 0732-183X (ISSN-L)
- 1527-7755
- OpenAlex
- W2146205118
- Cited by
- 339
- References
- 68
- FWCI
- 16.81
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.