Mutational analysis of apoptotic genes in familial aggregation of hematological malignancies

التفاصيل البيبلوغرافية
العنوان: Mutational analysis of apoptotic genes in familial aggregation of hematological malignancies
المؤلفون: Tetsuro Noguchi, Nouha Bouali, Sawsen Besbes, Paul Gesta, Violaine Bourdon, Walid Sabri Hamadou, Abderrahim Khelif, Hélène Dreyfus, Rahma Mani, Yosra Ben Youssef, Laurence Faivre, Zohra Soua, Hélène Zattara, Véronique Mari, Valérie Bonadona, Rym El Abed, Catherine Dugast, Hagay Sobol
المصدر: Bulletin du Cancer. 108:798-805
بيانات النشر: Elsevier BV, 2021.
سنة النشر: 2021
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Fas Ligand Protein, Tunisia, DNA Mutational Analysis, Mutation, Missense, Apoptosis, Biology, medicine.disease_cause, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Genetic variation, Gene expression, medicine, Humans, Family, Genetic Predisposition to Disease, Radiology, Nuclear Medicine and imaging, fas Receptor, Caspase 10, Gene, Alleles, Caspase 8, Perforin, Family aggregation, Cancer, Hematology, General Medicine, medicine.disease, Introns, Cross-Sectional Studies, 030104 developmental biology, Oncology, Hematologic Neoplasms, 030220 oncology & carcinogenesis, Cancer research, France, Carcinogenesis
الوصف: Summary Introduction Apoptosis deregulation have been associated to tumorigenesis process and was highlighted as a prominent hallmark of cancer. Several mutations have been reported in several forms of Blood cancer. However, it has never been investigated in familial aggregations of hematological malignancies. Methods In this study, we performed a mutational analysis by sequencing the entire coding regions in four key apoptotic genes FAS, FASLG, CASP8 and CASP10 in 92 independent families belonging to French and Tunisian populations and diagnosed with several forms of familial hematological malignancies. Results We report 15 genetic variations among which 7 were previously reported in several form of cancers and have a potential effect on gene expression. Particularly, the CASP8 variants p.Asp302His and p.Lys337Lys were detected in 15% and 10% of our group of patients respectively and were previously reported in association to breast cancer and to breast cancer susceptibility. Discussion In this study, we do not report the underlining deleterious mutations in familial hematological malignancies, but we describe some variants with potential risk of developing blood cancer. To gain further insights on the association between apoptosis pathway deregulation and familial hematological malignancies, more apoptotic genes should be investigated.
تدمد: 0007-4551
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00d3c5db6412681db8e8f39c18a11331Test
https://doi.org/10.1016/j.bulcan.2021.04.009Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....00d3c5db6412681db8e8f39c18a11331
قاعدة البيانات: OpenAIRE