Abstract Although small intestinal neuroendocrine tumours (SI‐NET) Grade 1 (G1) and 2 (G2) are often studied together, clinical course and response to treatment may differ. We hypothesized that these tumour groups express different markers in blood that may inform future treatment strategies. Blood from 107 SI‐NET patients (G1 n = 64, G2 n = 43) and 50
Malin Grönberg +2 more
wiley +1 more source
RET is a sex-biased regulator of intestinal tumorigenesis
Ret is implicated in colorectal cancer (CRC) as both a proto-oncogene and a tumor suppressor. We asked whether RET signaling regulates tumorigenesis in an Apc-deficient preclinical model of CRC.
Sean T. Koester +5 more
doaj +1 more source
Surgical Remission of Diabetes in a Patient With Mutation of RET Proto-Oncogene. [PDF]
Concepción Zavaleta MJ +7 more
europepmc +1 more source
RET Proto-Oncogene Mutational Analysis in 45 Iranian Patients Affected with Medullary Thyroid Carcinoma: Report of a New Variant. [PDF]
Damavandi E +6 more
europepmc +1 more source
Dual targeting of RET and SRC synergizes in RET fusion‐positive cancer cells
Rearranged during transfection (RET) fusions drive subsets of non‐small cell lung cancer (NSCLC) and papillary thyroid carcinoma (PTC). Despite new selective RET tyrosine kinase inhibitors (TKIs), resistance usually occurs and is often driven by RET ...
Juhyeon Son +13 more
doaj +1 more source
Advanced medullary thyroid cancer: pathophysiology and management
Carla Vaz Ferreira, Débora Rodrigues Siqueira, Lucieli Ceolin, Ana Luiza MaiaThyroid Section, Endocrine Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, BrazilAbstract: Medullary thyroid carcinoma (MTC) is a rare malignant ...
Ferreira CV +3 more
doaj
Roles of the RET Proto-oncogene in Cancer and Development. [PDF]
Takahashi M, Kawai K, Asai N.
europepmc +1 more source
Total colonic aganglionosis and cleft palate in a newborn with Janus-cysteine 618 mutation of RET proto-oncogene: a case report. [PDF]
Schierz IAM +6 more
europepmc +1 more source
MEN2 phenotype in a family with germline heterozygous rare RET K666N variant
Multiple endocrine neoplasia type 2 (MEN2) is a hereditary cancer syndrome caused by germline-activating pathogenic variants in the RET proto-oncogene.
A La Greca +8 more
doaj +1 more source
A Brief Review on The Molecular Basis of Medullary Thyroid Carcinoma
Approximately 5-10% of all thyroid cancers are medullary thyroid carcinomas (MTC). MTC is mainly sporadic in nature, but 20-30% of cases are hereditary. Genetic testing for hereditary MTC is very important for the patient and his family, but the patients
Mohammadi Masoumeh, Mehdi Hedayati
doaj

