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1.
Hematol Oncol ; 36(1): 320-323, 2018 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-28401573

RESUMEN

Castleman disease is a rare lymphoproliferative disorder with 2 distinctly defined clinical forms. While multicentric Castleman disease (UCD) poses a potential therapeutic challenge, unicentric variant has historically been considered curable with surgical resection. Hence, little is known to guide management of patients with UCD, refractory to surgical resection and combination chemotherapy. We present a case of a patient, negative for HIV and HHV-8, who had an unsuccessful surgical intervention and no response to radiotherapy and chemotherapy. He had severe paraneoplastic pemphigus and was treated with tocilizumab, an anti-interleukin-6 receptor monoclonal antibody that has demonstrated good response rates in multicentric Castleman disease but demonstrated no clinical response despite 2 months of treatment. Our report is the first to describe a lack of response to tocilizumab in the rare setting of refractory UCD and discuss potential for distinct disease biology.


Asunto(s)
Anticuerpos Monoclonales Humanizados/uso terapéutico , Enfermedad de Castleman/tratamiento farmacológico , Anticuerpos Monoclonales Humanizados/administración & dosificación , Anticuerpos Monoclonales Humanizados/farmacología , Enfermedad de Castleman/patología , Humanos , Masculino , Persona de Mediana Edad
2.
Nat Genet ; 41(2): 228-33, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19122663

RESUMEN

Marie Unna hereditary hypotrichosis (MUHH) is an autosomal dominant form of genetic hair loss. In a large Chinese family carrying MUHH, we identified a pathogenic initiation codon mutation in U2HR, an inhibitory upstream ORF in the 5' UTR of the gene encoding the human hairless homolog (HR). U2HR is predicted to encode a 34-amino acid peptide that is highly conserved among mammals. In 18 more families from different ancestral groups, we identified a range of defects in U2HR, including loss of initiation, delayed termination codon and nonsense and missense mutations. Functional analysis showed that these classes of mutations all resulted in increased translation of the main HR physiological ORF. Our results establish the link between MUHH and U2HR, show that fine-tuning of HR protein levels is important in control of hair growth, and identify a potential mechanism for preventing hair loss or promoting hair removal.


Asunto(s)
Hipotricosis/genética , Mutación Missense , Sistemas de Lectura Abierta/genética , Biosíntesis de Proteínas/genética , Factores de Transcripción/genética , Adolescente , Secuencia de Aminoácidos , Secuencia de Bases , Niño , China , Regulación hacia Abajo/genética , Familia , Femenino , Humanos , Masculino , Persona de Mediana Edad , Datos de Secuencia Molecular , Mutación Missense/fisiología , Linaje , Secuencias Reguladoras de Ácidos Nucleicos/fisiología , Homología de Secuencia de Ácido Nucleico
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