面部皮肤-粘膜静脉畸形可以独立于TEK基因突变而发生but可能与Src和p-Src的过度表达有关。

Nabila Brahami, Selvakumar Subramaniam, Moudjahed Saleh Al-Ddafari, Cecile Elkaim, Pierre-Olivier Harmand, Badr-Eddine Sari, Gérard Lefranc, Mourad Aribi
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引用次数: 3

摘要

我们的目的是寻找TEK基因的种系和体细胞DNA突变,并分析Src和磷酸Src (p-Src)在面部皮肤-粘膜静脉畸形(VMCM)患者的肿瘤和健康组织中的表达水平。在特莱姆森大学医学中心口腔外科和输血医学系分别从12个家庭和30个健康对照者中招募了符合条件的患者。直接DNA测序后进行Src和p-Src的免疫印迹分析。所有23个外显子及其5'和3'内含子侧翼区均未发现体细胞或种系突变,只有1例在内含子15处出现了c.3025+20-3025+22 del突变,在种系和体细胞DNA中均有发现。此外,Src和p-Src的表达水平升高仅在有这种突变的患者中观察到。然而,当归一化为β-肌动蛋白时,与健康组织相比,VMCM组织中Src和p-Src的总体相对表达水平显著增加(两种比较,p
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Facial cutaneo-mucosal venous malformations can develop independently of mutation of TEK gene but may be associated with excessive expression of Src and p-Src.

We aimed to search for mutations in the germline and somatic DNA of the TEK gene and to analyze the expression level of Src and phospho-Src (p-Src) in tumor and healthy tissues from patients with facial cutaneo-mucosal venous malformations (VMCM). Eligible patients from twelve families and thirty healthy controls were recruited respectively at the Departments of Stomatology and Oral Surgery, and Transfusion Medicine of Tlemcen University Medical Centre. Immunoblot analyses of Src and p-Src were performed after direct DNA sequencing. No somatic or germline mutations were found in all the 23 exons and their 5' and 3' intronic flanking regions, except for one case in which a c.3025+20-3025+22 del mutation was highlighted at the intron 15, both in the germline and somatic DNA. Additionally, elevated expression levels of Src and p-Src were observed only in the patient with such mutation. However, when normalized to β-actin, the overall relative expression levels of both Src and p-Src were significantly increased in VMCM tissues when compared to healthy tissues (for both comparisons, p <0.001). In conclusion, we confirm the outcomes of our previous work suggesting that VMCM can develop independently of mutation of the TEK gene. Additionally, the results for Src activity are of particular interest in the context of specific targeted therapies and biological diagnosis. Nevertheless, such a conclusion should be confirmed through a mechanistic study and/or in a satisfactory number of patients.

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