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Phenotype of melanocytes under physiological and pathological conditions
Strnadová, Karolína ; Lacina, Lukáš (advisor) ; Mokrý, Jaroslav (referee) ; Balvan, Jan (referee)
In addition to the dominant keratinocytes and fibroblasts, melanocytes are also indispensable representatives of skin cell populations. Melanocytes are pigment cells whose primary function is to produce the pigment melanin, which is important for protecting keratinocytes from harmful ultraviolet radiation. Excessive exposure to this radiation is a risk factor for the development of skin tumours, including malignant melanoma of the skin, in which pathological transformation of melanocytes into melanoma cells occurs. The presented thesis focuses on 4 thematic areas associated mainly with malignant melanoma. In the first thematic area, the increasing incidence of malignant skin melanoma is associated with the ageing of the population. One of the reasons seems to be the more frequent occurrence of proinflammatory setting in the ageing organism. It prepares a suitable environment for tumour development. The second thematic area focuses on new approaches that could expand the range of diagnostic methods for the early detection of malignant melanoma. The first approach methodically uses the detection of proinflammatory molecules in the patient's serum. Higher serum levels of IL-6 and IL-8 correlate with an unfavourable patient prognosis. The second approach is based on the possibility of detecting a...
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Role of Exosomes in the Progression, Diagnosis, and Treatment of Brain Tumors
Vaníková, Lucie ; Zíková, Martina (advisor) ; Lacina, Lukáš (referee)
Recent studies have confirmed the importance of extracellular vesicles, particularly exosomes, in the development of brain tumors. Considerable attention has been paid mainly to the influence of exosomes on biological processes in brain tumors. Exosomes mediate intercellular communication in the tumor microenvironment by transporting biomolecules. Most often they transmit various types of ribonucleic acids, specifically microRNAs, which affect the signalling pathways related to tumour growth in target cells. Thus, exosomes play an important role in tumor cell proliferation and differentiation, metastasis, and tumor resistance to chemotherapy or radiation. Due to their small size, exosomes can cross the blood-brain barrier and thus promote tumor progression. The topic of the bachelor thesis is a summary of the current knowledge on the role of exosomes in brain tumor progression, diagnosis and treatment.
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Study of Epithelial Mesenchymal Interactions in Squamous Epithelium Derived Tumors
Kodet, Ondřej ; Lacina, Lukáš (advisor) ; Borovanský, Jan (referee) ; Ehrmann, Jiří (referee)
This thesis is focused on the epithelial mesenchymal interactions in tumors derived from squamous epithelium including tumors arising from minor cell population (melanocytes). This study is also reflecting aspects of epithelial glycobiology resp. the study of endogenous lectins, the galectins, in head and neck squamous carcinomas. Galectins represent, in the current concepts of cell and tumor biology molecules with a remarkable potential. Galectins participate, besides in regulation of pre- and postnatal homeostasis in normal tissues, also in many pathological processes such as autoimmune reactions or malignancies. In this thesis, we demonstrated the presence of galectin-1 and -2 and their glycoligands in interphasic and mitotic nuclei, which may contribute to regulation of the cell cycle. Furthermore, we demonstrated galectin-9 as a sensitive marker of transformation normal to the dysplastic squamous epithelium in head and neck. The epithelial mesenchymal interactions represent mechanisms, which are responsible for dynamic maintenance of the homeostasis of the organism during prenatal development, postnatal growth and during cyclic renewal of certain tissues. These interactions also participate in wound healing. On the other hand they play a crucial role in the process of tumor transformation,...
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Study of Epithelial Mesenchymal Interactions in Squamous Epithelium Derived Tumors
Kodet, Ondřej ; Lacina, Lukáš (advisor) ; Borovanský, Jan (referee) ; Ehrmann, Jiří (referee)
This thesis is focused on the epithelial mesenchymal interactions in tumors derived from squamous epithelium including tumors arising from minor cell population (melanocytes). This study is also reflecting aspects of epithelial glycobiology resp. the study of endogenous lectins, the galectins, in head and neck squamous carcinomas. Galectins represent, in the current concepts of cell and tumor biology molecules with a remarkable potential. Galectins participate, besides in regulation of pre- and postnatal homeostasis in normal tissues, also in many pathological processes such as autoimmune reactions or malignancies. In this thesis, we demonstrated the presence of galectin-1 and -2 and their glycoligands in interphasic and mitotic nuclei, which may contribute to regulation of the cell cycle. Furthermore, we demonstrated galectin-9 as a sensitive marker of transformation normal to the dysplastic squamous epithelium in head and neck. The epithelial mesenchymal interactions represent mechanisms, which are responsible for dynamic maintenance of the homeostasis of the organism during prenatal development, postnatal growth and during cyclic renewal of certain tissues. These interactions also participate in wound healing. On the other hand they play a crucial role in the process of tumor transformation,...
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Glycophenotype of the Epidermis under Physiological and Pathological Conditions
Lacina, Lukáš ; Smetana, Karel (advisor) ; Zámečník, Josef (referee) ; Arenberger, Petr (referee)
Galectins-1,-3 and -7 are expressed in human epidermis. Galectin-1 and his binding sites are expressed there in the nuclei of cells which are closely related to or are identical with the stem cell population. Expression pattern of galectin-3 is differentiation-dependent in tissue as well as in vitro. Binding sites for this galectin are present in the similar manner. Expression of galectin-7 is not observed in differentiation-dependent manner. Binding sites for this member of galectins family were never observed in the epidermis. Galectin-2 is expressed in the nuclei of fibroblast under stress conditions. Expression of observed galectins and their binding sites in basal cell carcinoma and in psoriatic plaque refers to the differentiation level. We emphasize the lack of galectin-7 and binding sites for galectin-3 in basal cell carcinoma epithelium. Highly typical is abundant presence of galectin-1 in the stroma of basal cell carcinoma and in dermis of psoriatic plaque. We have also observed the dependence of galectin-7 expression on differentiation of squamous cell carcinoma. This relationship has no correlation to the survival of patients. The biological activity of stromal fibroblast toward to normal keratinocytes resulting in induction of "cancer-like" phenotype is the highlight of this study.
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