Mutated SON putatively causes a cancer syndrome comprising high-risk medulloblastoma combined with café-au-lait spots.
Celine ChiuStefanie LothMichaela KuhlenSebastian GinzelJörg SchaperThorsten RosenbaumTorsten PietschArndt BorkhardtJessica I HoellPublished in: Familial cancer (2019)
Medulloblastoma is the most frequent malignant brain tumor in childhood. This highly malignant neoplasm occurs usually before 10 years of age and more frequently in boys. The 5-year event-free survival rate for high-risk medulloblastoma is low at 62% despite a multimodal therapy including surgical resection, radiation therapy and chemotherapy. We report the case of a boy, who was born to consanguineous parents. Prominently, he had multiple café-au-lait spots. At the age of 3 years he was diagnosed with a high-risk metastatic medulloblastoma. The patient died only 11 months after diagnosis of a fulminant relapse presenting as meningeal and spinal dissemination. Whole-exome sequencing of germline DNA was employed to detect the underlying mutation for this putative cancer syndrome presenting with the combination of medulloblastoma and skin alterations. After screening all possible homozygous gene SNVs, we identified a mutation of SON, an essential protein in cell cycle regulation and cell proliferation, as the most likely genetic cause.
Keyphrases
- cell cycle
- cell proliferation
- free survival
- case report
- papillary thyroid
- radiation therapy
- genome wide
- squamous cell
- small cell lung cancer
- squamous cell carcinoma
- locally advanced
- copy number
- gene expression
- dna repair
- bone marrow
- spinal cord injury
- mesenchymal stem cells
- lymph node metastasis
- stem cells
- single molecule
- radiation induced
- preterm infants
- young adults
- gold nanoparticles
- dna damage
- early life
- small molecule
- quantum dots
- protein protein
- nucleic acid
- rectal cancer