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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

The role of the EP2 receptor for prostaglandin E2 in mouse skin carcinogenesis

Sung, You Me 28 August 2008 (has links)
Not available / text
2

Growth of immunogenic skin tumors: Infiltrating leukocytes

Chen, HwuDauRw, 1958- January 1989 (has links)
Subpopulations of tumor infiltrating leukocytes in immunogenic skin tumors were identified with monoclonal antibodies. The tumors studied included primary UV-induced tumors and JB/MS melanomas, which survive in the host by immunosuppression of the immune response. The proportions of nucleated cells in primary UV-induced tumor cell suspensions which reacted with monoclonal antibodies were: 52% Mac-1+, 21% Lyt-1+, 13% Lyt-2+, 7% L3T4+, and 8% IL-2R+. Thus there was a high proportion of cells of the macrophage lineage in the growing UV-induced tumors. In JB/MS melanoma cell suspensions the mean proportion of macrophages was 6.4%, and total T lymphocytes (Lyt-1) averaged only 5.5%. Thus, there was little leukocytes infiltration into JB/MS melanoma, suggesting that chemotaxis was defective. The high level of macrophages and T cells in the primary UV-induced tumors indicates that chemotaxis was intact. Therefore, either the tumorcidal capacities of the macrophages and Tc were insensitive to activated macrophages and to Tc cells.
3

Transcriptional regulation and the role of murine 8S-lipoxygenase in mouse skin carcinogenesis

Kim, Eunjung 28 August 2008 (has links)
Not available / text
4

Desenvolvimento de nanocarreadores multifuncionais para co-localização cutânea de agentes quimioterápicos. / Development of multifunctional nanocarriers for skin co-localization of chemotherapeutic agents.

Dartora, Vanessa Franco Carvalho 27 October 2016 (has links)
Visando o tratamento tópico de tumores cutâneos, desenvolvemos micro e nanoemulsões para a co-localização cutânea de paclitaxel e ceramida C6. A nanoemulsão mostrou-se mais eficaz em promover penetração de ambos os compostos nas camadas viáveis da pele, com aumentos de 11,5 (paclitaxel) e 3,5 (ceramida) vezes comparado a uma solução controle, e não reduziu significativamente a viabilidade de equivalentes epidérmicos, sugerindo sua segurança para aplicação tópica. A incorporação na nanoemulsão diminuiu as concentrações de paclitaxel e ceramida necessárias para reduzir a viabilidade de células de melanoma a 50% em 6 a 15 vezes, respectivamente, sendo que a co-encapsulação desses compostos promoveu uma nova redução (4 vezes) nessas concentrações, demonstrando aumento da eficácia decorrente da associação dos compostos. A administração tópica do nanocarreador contendo paclitaxel e ceramida co-encapsulados promoveu desorganização e morte celular em equivalentes cutâneos com melanoma, demonstrando o potencial desta formulação para o tratamento tópico de tumores cutâneos. / Nano and microemulsions were developed in this study for cutaneous co-localization of the active agents paclitaxel and C6 ceramide for topical treatment of skin cancer. The nanoemulsion was more effective in promoting the penetration of the compounds into viable skin layers, with increases of 11.5- (paclitaxel) and 3.5- fold (ceramide) being observed. The nanoemulsion did not reduce the viability of human epidermis equivalents, suggesting its safety for topical application. Incorporation in the nanoemulsion reduced the concentration of paclitaxel and ceramide required to decrease viability of human melanoma cells to 50% by 6 to 15-fold compared with their solutions; co-encapsulation of the compounds promoted a further reduction of 4-fold. Topical administration of the nanocarrier with co-encapsulated paclitaxel and ceramide to skin equivalents with melanoma promoted disorganization and intense cytotoxicity. These results demonstrate the potential of nanoemulsions for association of paclitaxel and ceramide C6 to improve their cytotoxic effect and skin localization.
5

Sarcoide equino / Equine sarcoid

Brum, Juliana Sperotto 17 September 2010 (has links)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Equine sarcoid is a locally aggressive cutaneous neoplasm, described and characterized as a clinical entity by Jackson in 1936. The neoplasm has a worldwide distribution and affects several equine species. It is believed that the cause of sarcoid is this infection by bovine papillomavirus 1 or 2. The combination of certain factors, including cutaneous trauma, genetic predisposition and viral exposure, seem to be involved in the development of the lesions. Sarcoid have no seasonality, no predilection by color or type hair and is considered the most common skin tumor of horses. Due to the lack of data which could characterize this tumor under the sphere of influence of the Laboratório de Patologia Veterinária (LPV) of the Universidade Federal de Santa Maria (UFSM), this dissertation determines the epidemiological aspects and the anatomic distribution of the different clinical forms of equine sarcoid in the state of Rio Grande do Sul. The files of histopathological exams carried out by the Laboratório de Patologia Veterinária of the Universidade Federal de Santa Maria (LPV-UFSM), between January 2000 and March 2010, were reviewed in search of cases of equine sarcoid. Forty cases were selected to determine epidemiological aspects and the anatomical distribution of the various clinical forms of these neoplasms in horses from Rio Grande do Sul. Out of the cases in which the ages were registered in the histopathological reports, 73,0% (27/37) were 1-5 years-old horses. Multiple sarcoids were observed in most of the affected horses (29/40 [72,5%]). The fibroblastic was the most observed clinical form and it occurred in 42,2% (27/64) of the cases. In more than half of the cases (22/40 [55,0%]), sarcoids had a multifocal distribution. Twenty two (55%) out of the 40 horses evaluated had the tumors in the limbs. / O sarcoide equino é um neoplasma cutâneo, localmente agressivo e foi descrito e caracterizado como uma entidade clínica por Jackson em 1936. Tem distribuição mundial e afeta várias espécies equídeas. Acredita-se que a causa seja a infecção pelo papilomavírus bovino tipo 1 ou 2. A combinação de alguns fatores, incluindo trauma cutâneo, predisposição genética e exposição ao vírus, parecem estar envolvidas no aparecimento das lesões. Não tem predileção por cor ou tipo da pelagem ou da pele e nem por estação do ano. O sarcoide é considerado o tumor mais comum de pele dos equinos. Devido a escassez de dados que caracterizam esse tumor na região de abrangência do Laboratório de Patologia Veterinária (LPV) da Universidade Federal de Santa Maria (UFSM), essa dissertação determina os aspectos epidemiológicos e a distribuição anatômica das diferentes formas clínicas do sarcoide no Rio Grande do Sul. Foram revisados todos os protocolos de exames histopatológicos, arquivados no LPV-UFSM, realizados entre janeiro de 2000 e março de 2010, na busca de casos de sarcoide equino. Quarenta casos foram selecionados com o objetivo de determinar os aspectos epidemiológicos e a distribuição anatômica das diferentes formas clínicas deste tumor em equinos no Rio Grande do Sul. Dos casos que tiveram suas idades anotadas nos protocolos, 73,0% (27/37) eram de equinos entre 1 e 5 anos de idade. Múltiplos sarcoides foram observados na maioria dos equinos afetados (29/40 [72,5%]). A forma clínica mais observada foi a fibroblástica, que ocorreu em 42,2% (27/64) dos casos. Em mais da metade dos casos (22/40 [55,0%]), os sarcoides tinham distribuição multifocal. Equinos que apresentavam tumores nos membros totalizaram 22 dos 40 (55%) casos analisados.
6

Mezibuněčné interakce v kožních nádorech. / Intercellular interactions in skin tumors.

Kučera, Jan January 2020 (has links)
The dissertation is focused on the study of intercellular interactions in skin tumors. It is based on 5 original publications that cover several topics. We studied the origin of tumor-associated fibroblasts concerning the primary tumor population. We demonstrated using a mouse model that tumor-associated fibroblasts are produced from the host organism and thus did not arise from transformation directly from tumor cells. We also investigated the relationship between tumor-associated fibroblasts and keratinocytes. We have shown that tumor-associated melanoma fibroblasts affect keratinocytes which, under their influence, acquire the features typically observed in migrating cells and cells undergoing epithelial-mesenchymal transition. We studied the interactions between healthy fibroblasts and tumor cells. We have demonstrated that fibroblasts acquired from healthy skin from a patient suffering from melanoma are significantly different from control fibroblasts of healthy donors in the expression profile. Changes in distal fibroblasts support the view of melanoma as a systemic disease. We have further demonstrated that melanoma-associated fibroblasts do not carry a BRAF mutation, in contrast to BRAF positivity of melanoma cells. And therefore, they did not arise from the transition from melanoma. The...

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