在有或没有卵巢塞尔托利-莱迪格细胞瘤的家族多元囊中发生的DICER1突变
Thomas Rio Frio1, Amin Bahubeshi, Chryssa Kanellopoulou
1Program in Cancer Genetics, Department of Oncology, McGill University Health Centre, Montreal, Quebec, Canada.
JAMA
|January 6, 2011
概括
生殖系DICER1突变与家族多元囊 (MNG) 和相关的Sertoli-Leydig细胞瘤 (SLCT) 有关,独立于多肺母细胞瘤. 这些突变破坏了microRNA表达模式.
科学领域:
- 遗传学 是一个遗传学.
- 在瘤学瘤学.
- 内分泌学 在内分泌学.
背景情况:
- 非有毒的多节 (MNG) 是常见的,但它的遗传基础是不太了解.
- 家庭MNG病例有时与卵巢塞尔托利-莱迪格细胞瘤 (SLCT) 一起发生.
- 生殖系DICER1突变涉及到肺母细胞瘤 (PPB),MNG和淋巴腺瘤.
研究的目的:
- 在没有PPB的情况下,调查家族MNG (有或没有SLCT) 和DICER1突变之间的关联.
- 确定DICER1突变是否有助于家族MNG和SLCT的遗传敏感性.
主要方法:
- 选了来自5个家庭的53个人 (2MNG,3MNG/SLCT) 检测DICER1突变.
- 分析了血液淋巴细胞和瘤组织的DICER1突变,失异性,基因表达和微RNA (miRNA) 失调.
主要成果:
- 在5个家族的37个个体中确定了生殖系DICER1突变.
- 描述了各种突变类型,包括蛋白质截断,框架内删除和误解突变.
- 在DICER1突变载体中观察到miRNA扰动,表明对基因调节的下游影响.
结论:
- DICER1突变与家族MNG和MNG与SLCT相关,无论PPB.
- 生殖系DICER1突变导致受影响个体miRNA表达模式的失调.
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