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

被引:11
作者
Frisk, Sofia [1 ,2 ]
Taylan, Fulya [1 ]
Blaszczyk, Izabela [3 ]
Nennesmo, Inger [4 ]
Anneren, Goran [5 ]
Herm, Bettina [6 ]
Stattin, Eva-Lena [5 ]
Zachariadis, Vasilios [1 ]
Lindstrand, Anna [1 ,2 ]
Tesi, Bianca [1 ,2 ]
Laurell, Tobias [1 ]
Nordgren, Ann [1 ,2 ]
机构
[1] Karolinska Inst, Ctr Mol Med, Dept Mol Med & Surg, Stockholm, Sweden
[2] Karolinska Univ Hosp, Karolinska Univ Lab, Dept Clin Genet, Stockholm, Sweden
[3] Umea Univ Hosp, Dept Surg & Perioperat Sci, Hand & Plast Surg, Umea, Sweden
[4] Karolinska Univ Hosp, Dept Pathol, Stockholm, Sweden
[5] Uppsala Univ, Dept Immunol Genet & Pathol, Sci Life Lab, Uppsala, Sweden
[6] Ostersunds Hosp, Child & Adolescent Habilitat Ctr, Ostersund, Sweden
基金
瑞典研究理事会;
关键词
accessory; cell fate; ectopic; muscle hypertrophy; muscular hypertrophy; PIK3CA; PROS; MARMORATA-TELANGIECTATICA-CONGENITA; SPECTRUM PROS; 4TH PATIENT; WILMS-TUMOR; NEPHROBLASTOMATOSIS; LANDSCAPE; DIAGNOSIS;
D O I
10.1111/cge.13543
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:118 / 125
页数:8
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