نتایج جستجو برای: braf mutation

تعداد نتایج: 295289  

Journal: :Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2014
M R Pelizzo C Dobrinja E Casal Ide M Zane O Lora A Toniato C Mian S Barollo M Izuzquiza J Guerrini N De Manzini I Merante Boschin D Rubello

BACKGROUND BRAF(V600E) mutation, which represents the most frequent genetic mutation in papillary thyroid carcinoma (PTC), is widely considered to have an adverse outcome on PTC outcome, however its real predictive value is not still well stated. The aim of the present study was to evaluate if BRAF(V600E) mutation could be useful to identify within patients with intrathyroid ultrasound-N0 PTC t...

2012
Dongjun Jeong Yujun Jeong Sungche Lee Hyeran Lee Wanju Lee Hyungjoo Kim Doosan Park Soyoung Park Wenxia Mu Hyun-Deuk Cho Mee-Hye Oh Sung Soo Lee Seung-Ha Yang Chang-Jin Kim

BACKGROUND Papillary thyroid carcinoma (PTC) of the thyroid is the most common endocrine malignancy. High prevalence of an activating point mutation of BRAF gene, BRAF(V600E), has been reported in PTC. We assessed the efficiency of peptide nucleic acid clamp real-time polymerase chain reaction (PNAcqPCR) for the detection of BRAF(V600E) mutation in PTC in comparison with direct sequencing (DS)....

Journal: :International journal of clinical and experimental medicine 2015
Qing-Feng Fu Peng-Tao Pan Le Zhou Xiao-Li Liu Feng Guo Li Wang Hui Sun

The goal of the present study was to evaluate the clinical and diagnostic value of both serum p53-antibodies (Abs) and preoperative fine needle aspiration cytology (FNAC) for BRAF mutation in patients with papillary thyroid carcinoma (PTC). A total of 312 patients, including thyroid adenoma (85) and PTC (227) were enrolled in this study. Two types of enzyme-linked immunosorbent assays (ELISA), ...

2015
Eleonora Monti Michela Bovero Lorenzo Mortara Giorgia Pera Simonetta Zupo Elena Gugiatti Mariella Dono Barbara Massa Gian Luca Ansaldo Giusti Massimo

Background. Molecular diagnostics has offered new techniques for searching for mutations in thyroid indeterminate lesions. The study's aim was to evaluate the BRAF mutations' incidence in an Italian regional population. Subjects and Methods. 70 Caucasian patients born in Liguria with indeterminate or suspicious cytological diagnoses. Results. A BRAF gene mutation was successfully analyzed in 56...

Journal: :Cellular signalling 2016
Maria Aguilar Hernandez Bipin Patel Fiona Hey Susan Giblett Hayley Davis Catrin Pritchard

The (V600E)BRAF oncogenic mutation is detected in a wide range of human cancers and induces hyperactivation of the downstream MEK-ERK signalling cascade. Although output of the BRAF-MEK-ERK pathway is regulated by feed-forward RAF activity, feedback control also plays an important role. One such feedback pathway has been identified in Caenorhabditis elegans and involves ERK-mediated phosphoryla...

2017
Sjors G. J. G. In’t Veld Kim N. Duong Mireille Snel Anke Witteveen Inès J. Beumer Leonie J. M. J. Delahaye Diederik Wehkamp René Bernards Annuska M. Glas Sun Tian

Colorectal cancer patients with the BRAF(p.V600E) mutation have poor prognosis in metastatic setting. Personalized treatment options and companion diagnostics are needed to better treat these patients. Previously, we developed a 58-gene signature to characterize the distinct gene expression pattern of BRAF-mutation-like subtype (accuracy 91.1%). Further experiments repurposed drug Vinorelbine a...

2013
Alexandra Thiel Ari Ristimäki

Different genetic aberrations of BRAF have been reported in various malignancies. BRAF is member of the RAS/RAF/MEK/ERK pathway and constitutive activity of this pathway can lead to increased cellular growth, invasion, and metastasis. The most common activating BRAF mutation in colorectal cancer is the V600E mutation, which is present in 5-15% of all tumors, and up to 80% of tumors with high mi...

2014
Bingfei Zhang Shu Liu Zhaoxia Zhang Jing Wei Yiping Qu Kexia Wu Qi Yang Peng Hou Bingyin Shi

BACKGROUND Thyroid nodules with indeterminate cytological features on fine needle aspiration biopsy specimens (FNABs) have a ~20% risk of thyroid cancer. BRAF(V600E) mutation and DNA methylation are useful markers to distinguish malignant thyroid neoplasm from benign. The aim of this study was to determine whether combined detection of BRAF(V600E) mutation and methylation markers on FNABs could...

2015
Tian Qiu Haizhen Lu Lei Guo Wenting Huang Yun Ling Ling Shan Wenbin Li Jianming Ying Ning Lv

BRAF mutations can be found in various solid tumors. But accurate and reliable screening for BRAF mutation that is compatible for clinical application is not yet available. In this study, we used an automated immunohistochemistry (IHC) staining coupled with mouse monoclonal anti-BRAF V600E (VE1) primary antibody to screen the BRAF V600E mutation in 779 tumor cases, including 611 colorectal carc...

2014
MELANIE SAINT - JEAN GAËLLE QUEREUX JEAN - MICHEL NGUYEN LUCIE PEUVREL ANABELLE BROCARD ANNE - CHANTAL KNOL AMIR KHAMMARI MARC G. DENIS

The relationship between BRAF mutations and the patient clinical profile is still under question. The objective of the present study was to correlate the BRAF mutation status in primary and metastatic melanomas with the clinicopathological profile, disease-free (DFS) and overall survival (OS). A total of 367 melanoma samples from 278 patients were screened for their BRAF status using a combinat...

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