Adrien Mouren, Albain Chansavang, Nadim Hamzaoui, Arunya Srikaran, Pierre Laurent-Puig, Laetitia Marisa, Sixtine De Percin, Audrey Lupo, Frédérique Larousserie, Hélène Blons, Anais L'Haridon, Nelly Burnichon, Eric Pasmant, Camille Tlemsani
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引用次数: 0
摘要
乳腺癌 1(BRCA1)基因的新生种系致病变体(gPV)非常罕见。迄今为止,只有少数病例被描述过,通常发生在有卵巢癌或乳腺癌病史的患者身上。在此,我们报告了第一例偶然发现的 BRCA1 基因致病变体,该变体是在 2025 年法国国家肿瘤测序计划 Plan France Médecine Génomique (PFMG) 框架内发现的。患者是一名29岁的男性,被诊断为转移性骨肉瘤。肿瘤全外显子组测序发现了一个 BRCA1 c.3756_3759del p.(Ser1253Argfs*10) 致病变异,但无杂合性缺失。较低的基因组不稳定性评分和同源重组缺陷的单碱基置换特征表明,BRCA1变体不是骨肉瘤肿瘤发生的驱动因素。种系全基因组测序确定了该变异体的种系性质,等位基因频率为36%,这表明该变异体是由合子后突变事件引起的嵌合体。原告的家人(父母和兄弟姐妹)都不是该变异体的携带者,这也证实了该变异体是全新出现的。像法国 PFMG 2025 这样的肿瘤测序计划已在全球范围内实施,可能有助于发现新的 gPV,包括新变异。
A de novo germline pathogenic BRCA1 variant identified following an osteosarcoma pangenomic molecular analysis.
De novo germline pathogenic variants (gPV) of the BReast CAncer 1 (BRCA1) gene are very rare. Only a few have been described up to date, usually in patients with a history of ovarian or breast cancer. Here, we report the first case of an incidental de novo BRCA1 germline pathogenic variant which was identified within the framework of the Plan France Médecine Génomique (PFMG) 2025 French national tumor sequencing program. The proband was a 29-year-old man diagnosed with metastatic osteosarcoma. Tumor whole exome sequencing identified a BRCA1 c.3756_3759del p.(Ser1253Argfs*10) pathogenic variant without loss-of-heterozygosity. A low genomic instability score and the absence of single base substitution signatures of homologous recombination deficiency suggested that the BRCA1 variant was not driver in the osteosarcoma tumorigenesis. Germline whole genome sequencing asserted the germline nature of this variant, with a 36% allele frequency, suggesting a mosaicism caused by a post-zygotic mutational event. The proband's family (parents and siblings) were not carriers of this variant confirming the de novo occurrence. Tumor sequencing programs like the French PFMG 2025 have been implemented worldwide and may help identify new gPV, including de novo variants.
期刊介绍:
In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers.
Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician.
The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.