RESUMEN
Cutaneous adnexal tumors form a vast heterogeneous group that include frequent entities that are mostly benign, as well as rare tumors that are occasionally malignant. In contrast to cutaneous tumors arising from the interfollicular epidermis that develop as a result of accumulation of UV-induced DNA damage (basal cell carcinoma, squamous cell carcinoma), the oncogenesis of adnexal tumors is related to a broad spectrum of genetic mechanisms (e.g., point mutation, fusion genes, viral integration, etc.). In this setting, specific and recurrent genetic alterations have been progressively reported, and these allow better classification of these entities. For certain of them, immunohistochemical tools are now available, enabling precise integrated histological and molecular diagnosis since certain entities are linked to well-defined alterations. In this context, we aim in this review to summarize the main molecular tools currently available for the classification of adnexal tumors.
Asunto(s)
Adenoma , Carcinoma Basocelular , Carcinoma de Células Escamosas , Neoplasias de Anexos y Apéndices de Piel , Neoplasias Cutáneas , Humanos , Neoplasias Cutáneas/genética , Neoplasias de Anexos y Apéndices de Piel/genéticaRESUMEN
Parosteal osteosarcomas and well-differentiated liposarcomas are both well-differentiated locally aggressive tumors. They both have simple karyotypes with amplification of the 12q13-15 regions including MDM2 and CDK4 genes. In this report, we describe the case of a parosteal osteosarcoma intertwined with a low-grade component similar to a well-differentiated liposarcoma. The association of a bone component with an adipose component was initially overlooked. We describe the histological, imaging, and molecular characteristics of this tumor stressing the importance of radio-pathological correlation. To our knowledge, this is the second report of a parosteal osteoliposarcoma. Awareness of this rare presentation may allow radiologists and surgeons to recognize the peripheral fatty component as an integral part of the tumor.
Asunto(s)
Neoplasias Óseas , Liposarcoma , Osteosarcoma , Neoplasias Óseas/diagnóstico por imagen , Quinasa 4 Dependiente de la Ciclina/genética , Humanos , Liposarcoma/diagnóstico por imagen , Osteosarcoma/diagnóstico por imagen , Proteínas Proto-Oncogénicas c-mdm2Asunto(s)
Antineoplásicos Inmunológicos , Melanoma , Neoplasias Cutáneas , Anticuerpos Monoclonales/uso terapéutico , Antineoplásicos Inmunológicos/uso terapéutico , Humanos , Melanoma/tratamiento farmacológico , Receptor de Muerte Celular Programada 1 , Neoplasias Cutáneas/tratamiento farmacológicoRESUMEN
The role of catalase on Saccharomyces cerevisiae replicative lifespan was investigated using a wild-type haploid laboratory yeast W303a, a catalase A mutant, a catalase T mutant and an acatalasaemic mutant. Lifespan analysis was performed in two different environmental conditions. Under repressing conditions, on glucose media, catalase T activity, but not catalase A activity was necessary to assure longevity. However, under derepressing conditions, on ethanol media, both catalases were required for longevity assurance. Although catalase activity and carbon source influence yeast lifespan, the relationship between oxidative defence and replicative senescence is complex.