Details

Autor(en) / Beteiligte

• Li, S.-L.
• Duo, L.-N.
• Wang, H.-J.
• Dai, W.
• Zhou, E.-Y.H.
• Xu, Y.-N.
• Zhao, T.
• Xiao, Y.-Y.
• Xia, L.
• Yang, Z.-H.
• Zheng, L.-T.
• Hu, Y.-Y.
• Lin, Z.-M.
• Wang, H.-N.
• Gao, T.-W.
• Ma, C.-L.
• Yang, Y.
• Li, C.-Y.

Titel

Identification of LCK mutation in a family with atypical epidermodysplasia verruciformis with T-cell defects and virus-induced squamous cell carcinoma

Ist Teil von

• British journal of dermatology (1951), 2016-12, Vol.175 (6), p.1204-1209

Ort / Verlag

England: Blackwell Publishing Ltd

Erscheinungsjahr

2016

Quelle

Wiley-Blackwell Journals

Beschreibungen/Notizen

• Summary Background Inherited epidermodysplasia verruciformis (EV) is a rare skin disorder characterized by susceptibility to specific types of human papilloma virus (HPV) and is strongly associated with skin carcinomas. Inactivating mutations in EVER1/EVER2 account for most cases of EV. However, more phenotypes related to but distinct from EV have been reported with an immunodeficiency state but without EVER1/EVER2 mutation, and the genetic basis for these atypical EV cases is poorly understood. Objectives To identify the causative gene responsible for three siblings affected by atypical EV but without EVER1/EVER2 mutation. Methods Whole‐exome sequencing followed by Sanger sequencing was performed to identify the gene responsible for the patients with atypical EV enrolled in our study. Results A homozygous splicing mutation was detected in LCK (c.188‐2A>G). This mutation resulted in an exon 3 deletion T lymphocyte‐specific protein tyrosine kinase isoform, which further led to frameshift mutation and subsequent mRNA decay. Conclusions We demonstrate a novel mutation in LCK in a family affected by atypical EV with T‐cell defects, HPV infection and virus‐induced malignancy, providing new clues in the understanding of host defences against HPV and better genetic counselling of patients with the EV phenotype. What's already known about this topic? Epidermodysplasia verruciformis (EV) is an unusual genodermatosis characterized by an increased susceptibility to β‐human papillomavirus and is associated with a high risk of skin carcinoma. Inactivating mutations in EVER1/EVER2 account for most cases of EV. What does this study add? Our study suggests an association between a novel splicing mutation in LCK and EV susceptibility. What is the translational message? Patients with EV should be tested for T lymphocyte‐specific protein tyrosine kinase deficiency and T‐cell function, which will help guide treatment. Linked Comment: Uitto and Vahidnezhad. Br J Dermatol 2016; 175:1138–1139.