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Wyszukujesz frazę "Urbańska, Krystyna" wg kryterium: Autor


Wyświetlanie 1-2 z 2
Tytuł:
Metastasis inhibition after proton beam, β- and γ-irradiation of melanoma growing in the hamster eye
Autorzy:
Romanowska-Dixon, Bożena
Elas, Martyna
Swakoń, Jan
Sowa, Urszula
Ptaszkiewicz, Marta
Szczygieł, Małgorzata
Krzykawska, Martyna
Olko, Paweł
Urbańska, Krystyna
Powiązania:
https://bibliotekanauki.pl/articles/1039523.pdf
Data publikacji:
2013
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
metastases
melanoma
ocular
proton beam
iodine-125
ruthenium-106
Opis:
Standard ocular tumor treatment includes brachytherapy, as well as proton therapy, particularly for large melanoma tumors. However, the effects of different radiation types on the metastatic spread is not clear. We aimed at comparing ruthenium (106Ru, emitting β electrons) and iodine (125I, γ-radiation) brachytherapy and proton beam therapy of melanoma implanted into the hamster eye on development of spontaneous lung metastases. Tumors of Bomirski Hamster Melanoma (BHM) implanted into the anterior chamber of the hamster eye grew aggressively and completely filled the anterior chamber within 8-10 days. Metastases, mainly in the lung, were found in 100% of untreated animals 30 days after enucleation. Tumors were irradiated at a dose of 3-10 Gy with a 106Ru plaque and at a dose of 6-14 Gy using a 125I plaque. The protons were accelerated using the AIC-144 isochronous cyclotron operating at 60 MeV. BHM tumors located in the anterior chamber of the eye were irradiated with 10 Gy, for the depth of 3.88 mm. All radiation types caused inhibition of tumor growth by about 10 days. An increase in the number of metastases was observed for 3 Gy of β-irradiation, whereas at 10 Gy an inhibition of metastasis was found. γ-radiation reduced the metastatic mass at all applied doses, and proton beam therapy at 10 Gy also inhibited the metastastic spread. These results are discussed in the context of recent clinical and molecular data on radiation effects on metastasis.
Źródło:
Acta Biochimica Polonica; 2013, 60, 3; 307-311
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Pulmonary metastases of the A549-derived lung adenocarcinoma tumors growing in nude mice. A multiple case study
Autorzy:
Jakubowska, Monika
Śniegocka, Martyna
Podgórska, Ewa
Michalczyk-Wetula, Dominika
Urbanska, Krystyna
Susz, Anna
Fiedor, Leszek
Pyka, Janusz
Płonka, Przemysław
Powiązania:
https://bibliotekanauki.pl/articles/1039526.pdf
Data publikacji:
2013
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
adenocarcinoma
histological analysis
metastases
nude mice
photodynamic therapy
zinc pheophorbide a
Opis:
Lung adenocarcinoma is a leading human malignancy with fatal prognosis. Ninety percent of the deaths, however, are caused by metastases. The model of subcutaneous tumor xenograft in nude mice was adopted to study the growth of control and photodynamically treated tumors derived from the human A549 lung adenocarcinoma cell line. As a side-result of the primary studies, observations on the metastasis of these tumors to the murine lungs were collected, and reported in the present paper. The metastasizing primary tumors were drained by a prominent number of lymphatic vessels. The metastatic tissue revealed the morphology of well-differentiated or trans-differentiated adenocarcinoma. Further histological and histochemical analyses demonstrated the presence of golden-brown granules in the metastatic tissue, similar to these found in the tumor tissue. In contrast to the primary tumors, the electron paramagnetic resonance spectroscopy revealed no nitric oxide - hemoglobin complexes (a source of intense paramagnetic signals), in the metastases. No metastases were found in other murine organs; however, white infarctions were identified in a single liver. Taken together, the A549-derived tumors growing subcutaneously in nude mice can metastasize and grow on site in the pulmonary tissue. Thus, they can represent an alternative for the model of induced metastatic nodule formation, following intravenous administration of the cancerous cells.
Źródło:
Acta Biochimica Polonica; 2013, 60, 3; 323-330
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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