2 research outputs found

    Analysis and characterization of proteins involved in epithelial plasticity during carcinomas tumor progression

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    [Resumen]: La mayor parte de los tumores son carcinomas que surgen como consecuencia de la alteraci贸n del fenotipo epitelial. En estadios tempranos de la progresi贸n tumoral, uno de los tiene lugar un proceso denominado transici贸n epitelio-mes茅nquima (TEM) caracterizado pores la p茅rdida de este fenotipo epitelial como consecuencia la destrucci贸n de las uniones adherentes, un tipo de uniones entre c茅lulas adyacentes implicado no s贸lo en el mantenimiento de la arquitectura tisular sino tambi茅n en la se帽alizaci贸n intracelular. La p茅rdida de la prote铆na E-cadherina en las uniones adherentes es un marcador estadios tempranos de la progresi贸n tumoral. Uno de los mecanismos implicados en la degradaci贸n de la E-cadherina es a trav茅s de la acci贸n de la prote铆na Hakai, una E3 ubiquitina-ligasa que se asocia a residuos de tirosina (Y) de la E-cadherina fosforilada por la quinasa Src, y que en consecuencia induce su ubiquitiniaci贸n y posterior degradaci贸n. La p茅rdida de estas uniones es un marcador del proceso de TEM en que las c茅lulas epiteliales pierden la polaridad apico-basal, adquieren capacidad migratoria e invasiva activ谩ndose el proceso de progresi贸n tumoral. Uno de los carcinomas m谩s frecuentes entre la poblaci贸n masculina es el adenocarcinoma acinar de pr贸stata, con una ratio de mortalidad asociada que lo sit煤a como el quinto m谩s letal entre los varones. Sintomatol贸gicamente, se caracteriza por la ausencia de s铆ntomas claros motivo por el cual se suele detectar ya en estados metast谩ticos. Se ha descrito extensamente el papel de la TEM en c谩ncer de pr贸stata, sin embargo, se conoce poco el papel de Hakai en la progresi贸n tumoral de este tipo de c谩ncer. En este trabajo se pretende determinar el posible papel de Hakai en c谩ncer de pr贸stata.[Resumo]: A maior parte dos tumores son adenocarcinmas que xorden como consecuencia da alteraci贸n do fenotipo epitelial. Un dos rasgos m谩is carater铆sticos da perda deste fenotipo 茅 a destruci贸n das uni贸ns adherentes, un tipo de asociaci贸n entre c茅lulas adxacentes implicado non s贸 no mantemento da arquitectura tisular senon na sinalizaci贸n intracelular. A perda de E-cadherina nas uni贸ns adherentes 茅 un marcador da perda destas uni贸ns. Un dos mecanismos implicados na degradaci贸n da E-cadherina 茅 a trav茅s da acci贸n da prote铆na Hakai, unha E3-ubiquitina ligasa que se asocia a residuos de tirosina (Y) da E-cadherina fosforilados pola quinasa Src e en consecuencia induce a sua ubiquitinaci贸n e posterior degradaci贸n. A perda destas uni贸ns 茅 un marcador do proceso de transici贸n epitelio-mes茅nquima (TEM) no que as c茅lulas epiteliais perden a polaridade apico-basal, adquiren capacidade migratoria e invasiva activ谩ndose o proceso de progresi贸n tumoral. Un dos carcinomas m谩is frecuentes entre a poboaci贸n masculina 茅 o adenocarcinoma acinar de pr贸stata, cunha ratio de mortalidade asociada que o sit煤a como o quinto m谩is letal entre os homes. Sintomatol贸xicamente, caracter铆zase pola ausencia de s铆ntomas claros motivo polo cal se soe detectar en estadios metast谩ticos. Describiuse de forma extensa o papel da TEM no cancro de pr贸stata. Non obstante, co帽ecese pouco sobre o papel de Hakai na progresi贸n tumoral deste tipo de cancro. Neste traballo pretendese determinar o posible papel de Hakai no cancro de pr贸stata.[Abstract]: Most of the tumors are carcinomas that arise as a consequence of the alteration of the epithelial phenotype. At early stages of tumor progression, one of the most characteristic features that takes place is a process named epithelial-to-mesenchymal transition (EMT) characterized by the loss of the epithelial phenotype as a consequence of the destruction of adherent junctions, a type of junction between sdjacent cells involved not only in the maintenance of tissue architecture but also in intracellular signaling. Loss of the E-cadherin protein at adherent junctions is a hallmark of early stages of tumor progression. One of the mechanisms involved in the degradation of E-cadherin is through the action of the Hakai protein, an E3 ubiquitin-ligase that is associated with tyrosine (Y) residues of E-cadherin phosphorylated by Src kinase, and consequently induces its ubiquitination and subsequent degradation. The loss of these junctions is a marker of the EMT process in which epithelial cells lose their apico-basal polarity, acquire migratory and invasive capacity, activating the process of tumor progression. One of the most frequent carcinomas among the male population is acinar adenocarcinoma of the prostate, with an associated mortality rate being the fifth most lethal cancer disease in men. Prostate cancer is characterized by the absence of clear symptoms, which is why it is usually detected in metastatic states. The role of the EMT in prostate cancer has been extensively described, however, little is known about Hakai's role in the tumor progression of this type of cancer. This work aims to determine the potential role of Hakai in prostate cancer.Traballo fin de mestrado (UDC.CIE). Biolox铆a molecular, celular e xen茅tica. Curso 2020/202

    Protein degradation by E3 ubiquitin ligases in cancer stem cells

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    Review[Abstract] Cancer stem cells are a small subpopulation within the tumor with high capacity for self-renewal, differentiation and reconstitution of tumor heterogeneity. Cancer stem cells are major contributors of tumor initiation, metastasis and therapy resistance in cancer. Emerging evidence indicates that ubiquitination-mediated post-translational modification plays a fundamental role in the maintenance of cancer stem cell characteristics. In this review, we will discuss how protein degradation controlled by the E3 ubiquitin ligases plays a fundamental role in the self-renewal, maintenance and differentiation of cancer stem cells, highlighting the possibility to develop novel therapeutic strategies against E3 ubiquitin ligases targeting CSCs to fight cancer.Instituto de Salud Carlos III; PI18/00121Instituto de Salud Carlos III; PI21/00238Xunta de Galicia; IN607B2020/1
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