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1.
Bull Exp Biol Med ; 171(1): 156-163, 2021 May.
Artículo en Inglés | MEDLINE | ID: mdl-34057619

RESUMEN

A correlation was found between chemoresistance of HT-29CD133+ and HT-29CD133- sublines obtained after cell sorting and high expression of CD133. On the other hand, knockout of the PROM1 gene and, as a consequence, the absence of CD133 expression did not increase the sensitivity of tumor cells to chemotherapy, which indicates the absence of a direct effect of CD133 on the formation of chemoresistance in colorectal cancer cells. Variants of the HT-29 line with complete or partial knockout of the PROM1 gene were equally sensitive to protein kinase inhibitors sorafenib and sunitinib. Notably, the highest resistance to mTOR inhibitors, temsirolimus and everolimus, was shown by cells with complete knockout of the PROM1 gene (KO-HT-29 (P1)). These findings suggest that CD133 is associated with the chemoresistance of colorectal cancer cells, but is not involved in its formation.


Asunto(s)
Adenocarcinoma , Neoplasias Colorrectales , Antígeno AC133/genética , Antígeno AC133/metabolismo , Adenocarcinoma/tratamiento farmacológico , Adenocarcinoma/genética , Adenocarcinoma/metabolismo , Línea Celular Tumoral , Neoplasias Colorrectales/tratamiento farmacológico , Neoplasias Colorrectales/genética , Neoplasias Colorrectales/patología , Resistencia a Antineoplásicos/genética , Células HT29 , Humanos , Células Madre Neoplásicas/metabolismo
2.
Bull Exp Biol Med ; 170(1): 135-141, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-33231806

RESUMEN

We studied the formation of spheroids by Caco-2, SW480, and HCT116 human colorectal adenocarcinoma cell lines under low-adhesion culturing conditions. Of these three cell lines, only HCT116 formed stable tumor spheroids. Flow cytometry analysis of 19 surface markers in monolayer HCT116 culture and spheroids formed by these cells revealed considerable similarity of the expression profiles in these two culturing modes. The only exception was EpCAM molecule: its expression in spheroids was 3-fold higher than in the monolayer culture. Scanning confocal laser microscopy showed equal EpCAM distribution in the inner mass of the spheroids.


Asunto(s)
Antígenos CD/genética , Antígenos de Neoplasias/genética , Molécula de Adhesión Celular Epitelial/genética , Regulación Neoplásica de la Expresión Génica , Esferoides Celulares/metabolismo , Antígenos CD/metabolismo , Antígenos de Neoplasias/metabolismo , Células CACO-2 , Línea Celular Tumoral , Molécula de Adhesión Celular Epitelial/metabolismo , Células HCT116 , Humanos , Esferoides Celulares/patología
3.
Bull Exp Biol Med ; 167(4): 541-545, 2019 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-31502129

RESUMEN

We studied proliferative activity of colorectal cancer cells with different expression level of CD133 molecule associated with cancer stem cells phenotype. Analysis of BrdU incorporation into Caco-2 and HT-29 cell lines showed that the percentage of cells in the DNA synthesis phase in the CD133+/high population is higher than in CD133-/low population. The expression of proliferation marker Ki-67 and the percentage of Ki-67+ cells were also higher in the CD133+/high population. Colorimetric analysis with crystal violet dye showed that the number of cells after 10-days culturing was higher in the CD133+/high population in both cell lines. These findings suggest that cells with high level of CD133 expression are characterized by higher proliferative activity, which can contribute to the tumor progression.


Asunto(s)
Antígeno AC133/metabolismo , Neoplasias Colorrectales/metabolismo , Neoplasias Colorrectales/patología , Células Madre Neoplásicas/metabolismo , Células Madre Neoplásicas/patología , Células CACO-2 , Proliferación Celular/fisiología , Colorimetría , Células HT29 , Humanos , Antígeno Ki-67/metabolismo
4.
Bull Exp Biol Med ; 166(1): 135-140, 2018 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-30417283

RESUMEN

The data on cancer stem cell surface molecular markers of 27 most common cancer diseases were analyzed using natural language processing and data mining techniques. As a source, 8933 full-text open-access English-language scientific articles available on the Internet were used. Text mining was based on searching for three entities within one sentence, namely a tumor name, a phrase "cancer stem cells" or its synonym, and a name of differentiation cluster molecule. As a result, a list of surface molecular markers was formed that included markers most frequently mentioned in the context of certain tumor diseases and used in studies of human and animal tumor cells. Based on similarity of the associated markers, the tumors were divided into five groups.


Asunto(s)
Biomarcadores/análisis , Células Madre Neoplásicas/metabolismo , PubMed , Minería de Datos , Bases de Datos Factuales , Internet , Procesamiento de Lenguaje Natural
5.
Bull Exp Biol Med ; 162(4): 552-557, 2017 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-28239798

RESUMEN

We studied immunosuppressive properties of skin fibroblasts and mesenchymal stromal cells against NK cells. In vitro experiments showed that mesenchymal stromal cells isolated from human umbilical cord and human skin fibroblasts can considerably attenuate cytotoxic activity of NK cells against Jurkat cells sensitive to NK-mediated lysis. NK cells cultured in lymphocyte population exhibited higher cytotoxic activity than isolated NK cells. Mesenchymal stromal cells or fibroblasts added 1:1 to lymphocyte culture almost completely suppressed NK cell cytotoxicity. This suggests that fibroblast-like cells can suppress not only isolated NK cells, but also NK cells in natural cell microenvironment.


Asunto(s)
Comunicación Celular/inmunología , Fibroblastos/metabolismo , Células Asesinas Naturales/efectos de los fármacos , Células Madre Mesenquimatosas/metabolismo , Técnicas de Cocultivo , Sangre Fetal/citología , Sangre Fetal/inmunología , Fibroblastos/citología , Fibroblastos/inmunología , Humanos , Interleucina-2/farmacología , Células Jurkat , Células Asesinas Naturales/citología , Células Asesinas Naturales/inmunología , Activación de Linfocitos/efectos de los fármacos , Células Madre Mesenquimatosas/citología , Células Madre Mesenquimatosas/inmunología , Cultivo Primario de Células , Piel/citología , Piel/inmunología
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