TY - JOUR
T1 - BRAF Mutation (V600E) Prevalence in Mexican Patients Diagnosed with Melanoma
AU - Zepeda-Lopez, Priscilla Denise
AU - Salas-Alanis, Julio Cesar
AU - Toussaint-Caire, Sonia
AU - Gutierrez-Mendoza, Daniela
AU - Vega-Memije, Elisa
AU - Lino Silva, Saúl
AU - Fajardo-RamÃrez, Oscar Raul
AU - Alcazar, Gregorio
AU - Moreno-Treviño, MarÃa Guadalupe
AU - Barrera Saldaña, Hugo Alberto
PY - 2016/5/20
Y1 - 2016/5/20
N2 - Background: B-Raf is a serine/threonine protein kinase activating the MAP kinase/ERK-signaling pathway. It has been shown that 50% of melanomas harbor activating BRAF mutations, with over 90% being the V600E mutation. Objective: The goal of this research was to determine the prevalence of the BRAF V600E mutation in patients from Central Mexico diagnosed with primary melanoma. Methods: Skin biopsies from 47 patients with melanoma were obtained from the dermatology department of the Hospital General 'Dr. Manuel Gea González' in Mexico City. For BRAF mutation determination, after DNA isolation, the gene region where the mutation occurs was amplified by PCR. Subsequently, the presence or absence of the V600E mutation was detected by Sanger sequencing performed at the private molecular diagnostic laboratory Vitagénesis in Monterrey, Mexico. Results: Of the 47 patients sampled, 6.4% harbored the V600E mutation. No statistical significance was found between mutations and the type of tumor.
AB - Background: B-Raf is a serine/threonine protein kinase activating the MAP kinase/ERK-signaling pathway. It has been shown that 50% of melanomas harbor activating BRAF mutations, with over 90% being the V600E mutation. Objective: The goal of this research was to determine the prevalence of the BRAF V600E mutation in patients from Central Mexico diagnosed with primary melanoma. Methods: Skin biopsies from 47 patients with melanoma were obtained from the dermatology department of the Hospital General 'Dr. Manuel Gea González' in Mexico City. For BRAF mutation determination, after DNA isolation, the gene region where the mutation occurs was amplified by PCR. Subsequently, the presence or absence of the V600E mutation was detected by Sanger sequencing performed at the private molecular diagnostic laboratory Vitagénesis in Monterrey, Mexico. Results: Of the 47 patients sampled, 6.4% harbored the V600E mutation. No statistical significance was found between mutations and the type of tumor.
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U2 - 10.1159/000445939
DO - 10.1159/000445939
M3 - Article
C2 - 27194985
SN - 1662-6575
VL - 9
SP - 241
EP - 245
JO - Case Reports in Oncology
JF - Case Reports in Oncology
IS - 1
ER -