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早期激活的体细胞 PIK3CA 突变促进异位肌肉发育和上肢过度生长。

Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth.

机构信息

Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.

Department of Clinical Genetics, Karolinska University Laboratory, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Clin Genet. 2019 Aug;96(2):118-125. doi: 10.1111/cge.13543. Epub 2019 May 9.

DOI:10.1111/cge.13543
PMID:30919936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6851821/
Abstract

PIK3CA-related overgrowth spectrum is a group of rare genetic disorders with asymmetric overgrowth caused by somatic mosaic PIK3CA mutations. Here, we report clinical data and molecular findings from two patients with congenital muscular upper limb overgrowth and aberrant anatomy. During debulking surgery, numerous ectopic muscles were found in the upper limbs of the patients. DNA sequencing, followed by digital polymerase chain reaction, was performed on DNA extracted from biopsies from hypertrophic ectopic muscles and identified the somatic mosaic PIK3CA hotspot mutations c.3140A > G, p.(His1047Arg) and c.1624G > A, p.(Glu542Lys) in a male (patient 1) and a female (patient 2) patient, respectively. Patient 1 had four ectopic muscles and unilateral isolated muscular overgrowth while patient 2 had 13 ectopic muscles and bilateral isolated muscular overgrowth of both upper limbs, indicating that her mutation occurred at early pre-somitic mesoderm state. The finding of PIK3CA mutations in ectopic muscles highlights the importance of PIK3CA in cell fate in early human embryonic development. Moreover, our findings provide evidence that the disease phenotype depends on the timing of PIK3CA mutagenesis during embryogenesis and confirm the diagnostic entity PIK3CA-related muscular overgrowth with ectopic accessory muscles.

摘要

PIK3CA 相关过度生长谱是一组罕见的遗传疾病,由体细胞镶嵌 PIK3CA 突变引起不对称过度生长。在这里,我们报告了两名先天性肌性上肢过度生长和异常解剖患者的临床数据和分子发现。在去瘤手术中,患者上肢发现了许多异位肌肉。对从肥大异位肌肉活检中提取的 DNA 进行 DNA 测序,随后进行数字聚合酶链反应,鉴定出男性(患者 1)和女性(患者 2)患者中体细胞镶嵌 PIK3CA 热点突变 c.3140A>G,p.(His1047Arg)和 c.1624G>A,p.(Glu542Lys)。患者 1 有四块异位肌肉和单侧孤立性肌肉过度生长,而患者 2 有 13 块异位肌肉和双侧上肢的双侧孤立性肌肉过度生长,表明她的突变发生在早期体节中胚层状态。异位肌肉中 PIK3CA 突变的发现强调了 PIK3CA 在人类胚胎早期发育中细胞命运中的重要性。此外,我们的发现提供了证据表明,疾病表型取决于胚胎发生过程中 PIK3CA 诱变的时间,并证实了 PIK3CA 相关肌肉过度生长伴异位副肌的诊断实体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f51/6851821/8f8bcda37825/CGE-96-118-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f51/6851821/f3f1ca0935dc/CGE-96-118-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f51/6851821/8f8bcda37825/CGE-96-118-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f51/6851821/f3f1ca0935dc/CGE-96-118-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f51/6851821/8f8bcda37825/CGE-96-118-g002.jpg

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