Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 22
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
Cytotechnology ; 71(5): 989-1002, 2019 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-31502069

RESUMEN

Cancer metastasis is believed to happen through active intravasation but there might be also another way to metastasize. According to passive shedding hypothesis, proposed by Munn et al., tumor cells detach from the tumor mass and passively shed to blood stream through leaky blood vessels. We propose a novel In Vitro Migrational Selection (IVMS) assay that enables the pre-selection of invasive pancreatic cancer Panc-02 cells and create a model of passive shedding. We established invasive sub-cell line of murine pancreatic cancer Panc-02 cells (refered to as Panc02-RS), which exhibited higher metastatic potential in vivo and at the same time decrease in vitro migratory skills, comparing to the initial Panc-02 cell line. In in vitro cell cultures Panc-02 spontaneously detached from the cell culture surface and later reattached and colonized new areas. We believe it can mimic the new way of metastasis, namely passive shedding. We concentrated on Panc-02 model but believe that IVMS might be used to create sub cell lines of many solid tumors to model passive shedding. Our results support the passive shedding hypothesis.

2.
J Biol Regul Homeost Agents ; 29(4): 823-8, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26753642

RESUMEN

The antiproliferative and immunomodulatory effects of melatonin (MLT) have been demonstrated in a variety of neoplasms including colorectal cancer (CRC). In humans and other mammals, MLT acts on target tissues through membrane and retinoid nuclear receptors. The aim of this study was to evaluate transcription activity of melatonin receptors and genes associated with regulation of their activity in colorectal adenocarcinoma tissues in relation to clinical stage of cancer. A total of 24 pairs of surgically removed tumoral and healthy (marginal) tissue samples from colorectal cancer patients at clinical stages I-II and III-IV were collected. As an additional control, twenty normal samples were tak¬en from people whose large intestine tissues were reported as non-tumoral after colonoscopy. Expression of mRNA genes was studied by microarray HG-U133A analysis. The analysis of gene expression profile was performed using commercially available oligonucleotide microarrays of HG-U133A. High increase of MT1 mRNA expression levels in all cancerous samples vs non-cancerous tissues was observed. The MT2 mRNA expression levels increased slightly in marginal and malignant samples. Among the genes participating in the cascade of signal transfer in cells activated by MLT via melatonin receptors, we found encoding genes (GNA11, OXTR, TPH1) only for differentiating stage III - IV of CRC. Monitoring the expression levels of genes that are related to melatonin receptors may offer a strategy to anticipate tumour development and estimate the molecular changes that occur during carcinogenesis. The mechanism behind this association needs further elucidation.


Asunto(s)
Neoplasias Colorrectales/metabolismo , Receptor de Melatonina MT1/genética , Receptor de Melatonina MT2/genética , Anciano , Neoplasias Colorrectales/genética , Neoplasias Colorrectales/patología , Humanos , Persona de Mediana Edad , Estadificación de Neoplasias , ARN Mensajero/análisis , Transcriptoma
3.
World J Urol ; 29(5): 677-82, 2011 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-21161538

RESUMEN

PURPOSE: Disorders of sex (DSD) development represent a serious condition. Most of the underlying mechanisms remain unclear. Disturbances within the androgen receptor (AR) pathway frequently account for 46 XY-DSDs. The individual gender-related outcome often is unsatisfactory. We present a long-term AR gene-mutation-associated follow-up in a group of 46 XY-DSD patients. METHODS: Twenty patients (46 XY) who underwent genitoplasty in infancy or early childhood were retrospectively identified. Median follow-up after surgery was 16 years. All were undervirilized at initial presentation. Thirteen had female gender assignment, and 7 were raised as males. A genital skin biopsy and subsequent fibroblast cultures were done. The specific binding of dihydrotestosterone, the thermostability of the receptor hormone complex, and 5-α-reductase activity were measured. AR gene mutations were detected by direct sequencing. The individual outcome was correlated with specific AR mutations. RESULTS: AR point mutations were detected in 12, 7 were previously unknown. There was no specific androgen binding in 3, reduced affinity in 9, and normal binding in 8 patients. 5-α-Reductase activity was normal in 15, reduced in 4 and completely absent in 1 patient. CONCLUSIONS: Retrospective evaluation revealed previously unknown and established AR gene mutations being associated with a distinct long-term outcome. Identification of the molecular mechanisms causing DSD will likely improve timely diagnosis and therapy. Exact characterization of AR activation and function may offer a treatment modality in affected patients. These data may allow us to give prognostic estimations on the individual outcome adding objective criteria for gender assignment in 46 XY-DSD patients.


Asunto(s)
Trastornos del Desarrollo Sexual/genética , Mutación , Receptores Androgénicos/genética , Adolescente , Niño , Preescolar , Femenino , Estudios de Seguimiento , Humanos , Masculino , Estudios Retrospectivos , Factores de Tiempo , Adulto Joven
4.
Leuk Lymphoma ; 48(3): 535-41, 2007 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-17454595

RESUMEN

We summarized registry data of the long term observation of 35 patients treated with two autologous transplants. Prognostic factors for overall survival (OS) and DFS were analyzed. The OS was compared with 105 patients from a single transplant group. Two factors were significant in univariate analysis of DFS after the second transplant: response to the first transplant (complete remission (CR) versus progressive disease (PD) p = 0.041) and the disease status at the time of the second autologous stem cell transplantation (ASCT) (CR versus partial remission (PR) p = 0.004; CR versus PD p = 0.0002). In the multivariate analysis only the last of the parameters remain significant (RR 2.30, p = 0.004, 95% CI; 1.30 - 4.04). In the analysis of OS, two factors were significant in univariate analysis: status of the disease at the first transplant (PR versus PD p = 0.008) and response to the first transplant (CR versus PD p = 0.025). None of those factors remained significant in a multivariate analysis. A probability of 5-year survival after the first transplant in patients treated with two transplants was 83% (95% CI; 70 - 97%). A tendency towards better survival was seen in patients treated with two transplants (p = 0.01). The trend toward better survival from the time of diagnosis is kept for those who entered CR or PR after standard chemotherapy (p = 0.097) but not for the whole group (p = 0.13).


Asunto(s)
Trasplante de Células Madre Hematopoyéticas , Enfermedad de Hodgkin/terapia , Adolescente , Adulto , Femenino , Humanos , Linfoma no Hodgkin/terapia , Masculino , Persona de Mediana Edad , Pronóstico , Inducción de Remisión , Tasa de Supervivencia , Trasplante Autólogo , Resultado del Tratamiento
5.
Ann Oncol ; 15(8): 1222-30, 2004 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-15277262

RESUMEN

BACKGROUND: The reported probability of survival of patients with Hodgkin's disease (HD) following high-dose chemotherapy with autologous stem cell transplantation (HDC/ASCT) is 35-65% at 5 years. The Polish Lymphoma Research Group investigated retrospectively prognostic factors for overall survival (OS) and event-free survival (EFS), and the risk of secondary malignancies in a large series of patients who underwent HDC/ASCT. PATIENTS AND METHODS: The data of 341 consecutive patients treated in 10 centers from 1990 to 2002 were collected and analyzed. RESULTS: The actuarial 5-year OS and EFS were 64% [95% confidence interval (CI) 57% to 71%] and 45% (95% CI 39% to 51%), respectively. In the multivariate model, unfavorable prognostic factors for EFS were less than partial response at the time of ASCT [relative risk (RR), 2.92 (95% CI 1.68-5.08); P<0.001] and three or more previous chemotherapy lines (RR, 2.16; 95% CI 1.42-3.30; P<0.001). These two factors were also associated with unfavorable OS (RR, 3.32; 95% CI 1.90-5.79; P<0.001 and RR, 2.34, 95% CI 1.51-3.64; P<0.001). Five-year cumulative risk of secondary malignancy was 8.4% (95% CI 2% to 13%) and the only identified risk factor was splenectomy (P=0.02). CONCLUSIONS: HDC/ASCT should be considered early in the course of disease for patients with a response after standard therapy.


Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Enfermedad de Hodgkin/tratamiento farmacológico , Trasplante de Células Madre , Adolescente , Adulto , Niño , Preescolar , Supervivencia sin Enfermedad , Relación Dosis-Respuesta a Droga , Femenino , Humanos , Masculino , Persona de Mediana Edad , Neoplasias Primarias Secundarias , Pronóstico , Estudios Retrospectivos , Factores de Riesgo , Trasplante Autólogo , Resultado del Tratamiento
6.
Bone Marrow Transplant ; 33(12): 1225-9, 2004 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-15094747

RESUMEN

Our previously published study showed promising results of autologous stem cell transplantation (ASCT) in patients with primary resistant Hodgkin's disease (HD). Probabilities of overall survival (OS) and progression-free survival (PFS) at 3 years were 55 and 36%, respectively. The present study was undertaken to compare these results with conventionally treated patients and thus evaluate therapeutic options. Retrospective data on 76 adult patients who underwent ASCT were matched with 76 conventionally treated patients from 17 centers. Comparison of clinical characteristics in both groups showed that ASCT patients were younger (24 vs 31.5 years, P=0.001), more frequently presented with 'B' symptoms (P=0.03) and that more patients treated with chemotherapy (CT) had elevated LDH (P=0.03). In univariate analyses, bulky disease (P=0.0043) and complete resistance to standard CT (P=0.051) were found to be risk factors for OS. In a multivariate survival analysis only bulky disease was found to an independent prognostic factor (P=0.005). There was no difference in survival between the treatment groups with 5 years OS 33.7 (CI: 23-46) in the ASCT group and 35.6% (CI: 25-50) for the CT group (P=0.92). We conclude that ASCT is not superior to standard CT for treatment of patients with primary refractory HD.


Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Trasplante de Médula Ósea/métodos , Enfermedad de Hodgkin/terapia , Adolescente , Adulto , Trasplante de Médula Ósea/mortalidad , Niño , Femenino , Enfermedad de Hodgkin/mortalidad , Humanos , Masculino , Persona de Mediana Edad , Análisis Multivariante , Pronóstico , Estudios Retrospectivos , Factores de Riesgo , Terapia Recuperativa/métodos , Análisis de Supervivencia , Acondicionamiento Pretrasplante
7.
Bone Marrow Transplant ; 30(1): 29-34, 2002 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12105774

RESUMEN

We analysed the treatment outcome of primary refractory HD patients managed with high-dose chemotherapy and haematopoietic cell transplantation. Data of 65 adult patients who underwent HDC/ASCT in nine Polish centres for primary resistant Hodgkin's disease between June 1991 and July 2000 were collected retrospectively. Response rate to HDC/ASC: CR, 54%; PR, 20%; less than PR, 15%; early deaths, 11%. Actuarial 3-year OS and PFS were 55% and 36%, respectively. In multivariate analysis, lack of bulky lymph nodes and use of immunotherapy were favourable factors for both OS and PFS. IPF <3 at the time of transplantation was predictive for PFS. However, the prognostic impact of immunotherapy should be interpreted with caution since this group included more patients who achieved CR after HDC/ASCT. The results of HDC/ASCT are encouraging and confirm earlier findings. The role of immunotherapy should be further investigated in prospective trials.


Asunto(s)
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Trasplante de Células Madre Hematopoyéticas/mortalidad , Enfermedad de Hodgkin/terapia , Adolescente , Adulto , Análisis de Varianza , Niño , Femenino , Enfermedad de Hodgkin/mortalidad , Humanos , Inmunoterapia , Masculino , Persona de Mediana Edad , Pronóstico , Estudios Retrospectivos , Terapia Recuperativa , Análisis de Supervivencia , Tasa de Supervivencia , Trasplante Autólogo/mortalidad , Resultado del Tratamiento
8.
Folia Biol (Krakow) ; 49(1-2): 1-12, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11732159

RESUMEN

Chick embryo fibroblasts (CEFs) spontaneously form multicellular and multilayered sheets suspended on the network of glass fibres which are stabilized by fibronectin containing protein deposits located at cell-to-cell contacts. The cells situated within the sheets are surrounded by the neighbouring cells and their mechanical equilibrium is stabilised by intercellular "parabaric" effects. It was found that CEFs in the sheets retain relatively high mitotic activity corresponding to that observed in sparse monolayer cultures. These cells grew up to much higher local density than in confluent and contact-inhibited monolayer cultures and developed an abundance of microfilament bundles that terminated at vinculin-containing protein complexes. The results presented demonstrate that direct contact with solid substratum, cell-to-cell contacts, local cell density, and intercellular exchange of humoral factors are not directly involved in the density-dependent inhibition of growth observed in monolayer cultures. They also support the concepts concerning the role of mechanical equilibrium of cell membrane and sub-membranous cytoskeleton in the regulation of proliferation of non-transformed cells.


Asunto(s)
Técnicas de Cultivo de Célula/métodos , ADN/biosíntesis , Fibroblastos/metabolismo , Citoesqueleto de Actina/metabolismo , Animales , Embrión de Pollo , Fibroblastos/citología , Fibronectinas/metabolismo , Procesamiento de Imagen Asistido por Computador , Inmunohistoquímica , Locomoción/fisiología , Microscopía Confocal , Mitosis/fisiología
9.
Mech Dev ; 105(1-2): 93-104, 2001 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-11429285

RESUMEN

Here, we describe the generation of viable and dopamine-producing neurons derived from pluripotent mouse embryonic stem cells. Neurotrophic factors in combination with survival-promoting factors, such as interleukin-1beta, glial cell line-derived neurotrophic factor, neurturin, transforming growth factor-beta(3) and dibutyryl-cyclic AMP, significantly enhanced Nurr1 and tyrosine hydroxylase (TH) mRNA levels, whereas En-1, mash-1 and dopamine-2-receptor mRNA levels were not upregulated. In parallel, mRNA levels of the anti-apoptotic gene bcl-2 were found to be upregulated at terminal stages. Double immunofluorescence analysis revealed increased numbers of TH- and dopamine transporter-, but not gamma-aminobutyric acid- and serotonin-positive neurons in relation to synaptophysin-labeled cells by survival-promoting factors. Moreover, high-performance liquid chromatography analysis showed detectable levels of intracellular dopamine. We conclude that survival-promoting factors enhance differentiation, survival and maintenance of dopaminergic neurons derived from embryonic stem cells.


Asunto(s)
Dopamina/biosíntesis , Neuronas/citología , Neuronas/metabolismo , 1-Metil-4-fenil-1,2,3,6-Tetrahidropiridina/farmacología , Animales , Apoptosis , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico , Bucladesina/metabolismo , Diferenciación Celular , Supervivencia Celular , Cromatografía Líquida de Alta Presión , Proteínas de Unión al ADN/biosíntesis , Dopamina/metabolismo , Fibroblastos/metabolismo , Proteínas de Homeodominio/biosíntesis , Inmunohistoquímica , Ratones , Microscopía Fluorescente , Miembro 2 del Grupo A de la Subfamilia 4 de Receptores Nucleares , Proteínas Proto-Oncogénicas c-bcl-2/biosíntesis , ARN Mensajero/metabolismo , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Serotonina/biosíntesis , Factores de Tiempo , Factores de Transcripción/biosíntesis , Factores de Transcripción/metabolismo , Factor de Crecimiento Transformador beta/metabolismo , Factor de Crecimiento Transformador beta3 , Tirosina 3-Monooxigenasa/metabolismo , Regulación hacia Arriba , Ácido gamma-Aminobutírico/biosíntesis
10.
J Mol Cell Cardiol ; 33(3): 521-32, 2001 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-11181020

RESUMEN

beta(1)integrin-deficient (beta(1)-/-) ES cells showed increased differentiation of cardiac cells characterized by reduced adhesion and high beating frequency. Whereas in whole embryoid body outgrowths of beta(1)-/- cells maximum levels of alpha(v), beta(3)and beta(5)integrin mRNA were delayed and transiently upregulated, in cardiac clusters isolated from beta(1)-/- cells, only beta(3)integrin mRNA levels were enhanced in comparison to wild-type (wt) cells. To answer the question, whether alpha(v)and beta(3)integrins may compensate, at least partially, the loss of beta(1)integrin function during cardiac differentiation, the distribution of alpha(v)and beta(3)integrins in beta(1)-/- and wt pacemaker-like cardiac cells was analyzed. A different distribution of alpha(v)and beta(3)integrins in beta(1)-/- v wt cardiac cells was found. In wt cardiac cells, beta(1)integrin was localized in specialized subsarcolemmal regions, in particular, at focal contacts and costameres, but alpha(v)integrin was diffusely distributed. In contrast, in beta(1)-/- cardiac cells, alpha(v)integrin was preponderantly localized at cell membranes, focal contacts and costameres. beta(3)integrin displayed a diffuse pattern both in wt and in beta(1)-/- pacemaker-like cells at early differentiation stages, whereas at terminal stages, beta(3)was colocalized with sarcomeres in wt, but not in beta(1)-/- pacemaker-like cells. Quantitative immunofluorescence analysis revealed increased alpha(v)and beta(3)integrin levels in beta(1)-/- pacemaker-like cardiac cells. Our results led us to conclude that altered cellular distribution of alpha(v)integrin and upregulation of beta(3)integrin correlate with growth and survival of beta(1)-/- cardiac pacemaker-like cells at an early developmental state. However, alpha(v)and beta(3)integrins cannot functionally compensate the loss of beta(1)integrin during terminal differentiation of cardiac cells implicating that cardiomyocytes require specific beta(1)integrin functions for cardiac specialization.


Asunto(s)
Antígenos CD/metabolismo , Cadenas beta de Integrinas , Integrina beta1/fisiología , Glicoproteínas de Membrana Plaquetaria/metabolismo , Animales , Antígenos CD/genética , Adhesión Celular , Células Cultivadas , Corazón/embriología , Humanos , Integrina alfaV , Integrina beta1/metabolismo , Integrina beta3 , Integrinas/genética , Ratones , Ratones Noqueados , Glicoproteínas de Membrana Plaquetaria/genética , ARN Mensajero , Células Madre/citología , Regulación hacia Arriba
11.
Differentiation ; 68(4-5): 167-74, 2001 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11776469

RESUMEN

Embryonic stem (ES) cells have the capacity to self renew and to differentiate into cellular derivatives of the endodermal, ectodermal, and mesodermal lineages. Therefore, ES cells have been used to analyse the effects of exogenous factors on the developmental pattern during in vitro differentiation. By using an in vitro loss-of-function approach based on beta1 integrin-deficient ES cells, it was found that integrin-dependent mechanisms are involved in the regulation of Wnt-1 and BMP-4 expression. Antagonistic effects of the signalling molecules Wnt-1 and BMP-4, morphogens involved in early differentiation events, have been observed in vivo and in vitro: BMP-4 acts as a potent mesoderm inducer, whereas Wnt-1 plays a critical role in the determination of neuroectoderm. Here, we summarise data of ES cell-derived cardiac, myogenic, and neuronal differentiation of wild type and beta1 integrin-deficient ES cells. We present evidence that the interaction of cells with the extracellular matrix via integrins determines the expression of the signalling molecules BMP-4 and Wnt-1, resulting in the activation of the mesodermal and neuroectodermal lineage, respectively. The results support the idea that the influence of the extracellular 'niche' on the developmental fate of pluripotent stem cells is determined not only by soluble factors, but also by the extracellular matrix.


Asunto(s)
Diferenciación Celular , Embrión de Mamíferos/citología , Células Madre/fisiología , Proteínas de Pez Cebra , Animales , Proteína Morfogenética Ósea 4 , Proteínas Morfogenéticas Óseas/fisiología , Regulación del Desarrollo de la Expresión Génica , Corazón/embriología , Humanos , Integrina beta1/fisiología , Neuronas/fisiología , Proteínas Proto-Oncogénicas/fisiología , Proteínas Wnt , Proteína Wnt1
12.
Med Oncol ; 18(2): 141-8, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11778760

RESUMEN

The objective of this multiinstitutional study was to evaluate the safety and efficacy of rituximab at standard four weekly doses in patients with recurrent indolent lymphoma. Thirty-eight patients entered into this study, 63% had follicular lymphoma and 61% had an IPI score of 2 or more. Median disease duration was 3 yr, median number of prior treatments was three, and 66% of patients responded to the immediate past treatment with a median remission duration of 3 mo. A total of 158 antibody doses were given, including two patients who received two courses of four infusions each. One patient developed acute respiratory failure after the second dose and required assisted ventilation. There was no immediate relationship to the antibody infusion and no evidence of infection. This complication resolved and the patient successfully completed the full course of the antibody treatment. Another patient discontinued therapy after the second dose owing to intolerable fever and painful erythema. Sixty percent of the first, and 20% of subsequent rituximab infusions were associated with infusion-related reactions including mild fever, chills, and occasional skin eruptions. Complete and partial responses were achieved in 24% and 35% of 34 evaluable patients, respectively, for an overall response rate of 59%. The median time to progression/relapse in responding patients was 16 mo (95% CI, 6.4, 25.6) compared with a median of 3 mo duration of response to the immediate previous therapy in these patients. Longer response duration post rituximab monotherapy than with previous treatment in this series of heavily pretreated patients suggests a major role for the antibody in the therapy of patients with indolent lymphoma.


Asunto(s)
Anticuerpos Monoclonales/uso terapéutico , Antineoplásicos/uso terapéutico , Linfoma Folicular/tratamiento farmacológico , Adulto , Anciano , Anticuerpos Monoclonales/efectos adversos , Anticuerpos Monoclonales de Origen Murino , Antineoplásicos/efectos adversos , Progresión de la Enfermedad , Supervivencia sin Enfermedad , Femenino , Humanos , Infusiones Intravenosas , Linfoma Folicular/patología , Masculino , Persona de Mediana Edad , Recurrencia , Insuficiencia Respiratoria/inducido químicamente , Rituximab , Resultado del Tratamiento
13.
Exp Cell Res ; 255(1): 40-6, 2000 Feb 25.
Artículo en Inglés | MEDLINE | ID: mdl-10666332

RESUMEN

A method is described which reliably quantifies the degree of intercellular communication via gap junctions by combining a dye-loading technique with fluorescence-activated flow cytometry. Our experiments expand former measurements of other groups by analyzing the time- and density-dependent onset of coupling with a fixed ratio of donor to recipient cells. The high sensitivity of this technique provides a better resolution than the microelectrode technique and allows the detection of small changes in gap-junctional coupling by examining a large number of cells in a single experiment. Suspended cells were loaded with the membrane-permeable dye calcein AM, which is intracellularly hydrolyzed by nonspecific esterases, and the resulting polyanionic calcein is thus trapped inside these donor cells. Gap junctions, however, are permeable for this fluorescent dye, as can be observed when suspended donor cells are added to recipient cells (i.e., monolayer cultures) in which case cell-cell contact is established within less than 60 min. In addition, one of these two cell populations can also be stained with a membrane-resident dye (e.g., DiI), which facilitates the identification of different cell populations (donors, recipients, and noncoupled cells) not only by epifluorescence microscopy but also by flow cytometry. Our analyses reveal that junctional coupling depends not only on the connexin type (homo- or heterotypic junction) but also on the origin (species) of the contacting cells (homo- or heterospecific contact). We confirm earlier reports in which homotypic-homospecific coupling was demonstrated with different techniques in connexin-transfected HeLa and RIN cells as well as in BICR/M1R(k) and 3T3/SV40 cells. In contrast to other publications, we show that a significant heterotypic-homospecific coupling between Cx40- and Cx43-HeLa transfectants can be resolved, whereas no coupling was detected for heterotypic-heterospecific contacts between Cx40-HeLa transfectants and the Cx43-expressing cell lines BICR/M1R(k), 3T3/SV40, and RIN.


Asunto(s)
Citometría de Flujo/métodos , Uniones Comunicantes/fisiología , Células 3T3 , Animales , Comunicación Celular/fisiología , Recuento de Células , Fluoresceínas/metabolismo , Colorantes Fluorescentes/metabolismo , Células HeLa , Humanos , Ratones , Ratas , Células Tumorales Cultivadas
14.
Biochem Cell Biol ; 77(2): 133-40, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-10438148

RESUMEN

The effects of cyclosporin A (CsA), a clinically used immunosupressive drug, on contractile activity of chick cardiomyocytes grown as small aggregates or explants suspended on a network of elastic glass fibres or cultured in a monolayer were analysed in vitro with computer-aided image cytometry methods. At therapeutic concentrations (200-1500 ng/mL), CsA induced changes in the frequency and amplitude of the beating activity of cardiomyocytes 15 min after application. Longer treatment of cardiomyocytes, for 20-24 h, additionally induced changes in their shape and cytoskeleton organization (F-actin and alpha-actinin distribution). These results indicate that CsA is able to affect directly the contractile activity, morphology, and cytoskeleton architecture of heart cells.


Asunto(s)
Ciclosporina/farmacología , Citoesqueleto/efectos de los fármacos , Corazón/efectos de los fármacos , Contracción Miocárdica/efectos de los fármacos , Miocardio/citología , Animales , Células Cultivadas , Embrión de Pollo , Citoesqueleto/ultraestructura , Corazón/embriología , Corazón/fisiología , Técnicas In Vitro
16.
Pol Arch Med Wewn ; 95(5): 453-8, 1996 May.
Artículo en Polaco | MEDLINE | ID: mdl-8848413

RESUMEN

The study was aimed to assess the efficacy of busulphan treatment in patients with polycythemia rubra vera (PRV). The group of 74 patients (mean age 60 years, range: 40-81) was studied, including 38 females, 36 males. The remission was achieved in all cases; the mean time of remission was 33 months (range 3-200), the mean busulphan dose necessary to reach the first PRV remission was 266 mg (range: 76-600). The associations between hemoglobin level, white blood cells, neurocytes, platelet counts at diagnosis and the mean cumulative busulphan dose necessary to obtain the first PRV remission as well as between above parameters and the mean duration of the first PRV remission was estimated. The mean duration of the first PRV remission was significantly (P < 0.03) longer in patients with neurocyte count below 9.6 G/l (9.6 x 10(3)/mm3) as compared to those with higher levels; except it, no relationship were noticed between above parameters. The results of the study confirmed that busulphan is an effective and safe drug for patients with PRV.


Asunto(s)
Busulfano/uso terapéutico , Policitemia Vera/tratamiento farmacológico , Adulto , Anciano , Anciano de 80 o más Años , Busulfano/farmacología , Femenino , Humanos , Recuento de Leucocitos/efectos de los fármacos , Masculino , Persona de Mediana Edad , Recuento de Plaquetas/efectos de los fármacos , Policitemia Vera/sangre , Inducción de Remisión
17.
Biochem Cell Biol ; 73(7-8): 431-9, 1995.
Artículo en Inglés | MEDLINE | ID: mdl-8703415

RESUMEN

Heart cells continue to contract rhythmically after isolation and in culture in vitro. We describe a model of heart preparation in vitro that permits quantitative research on the frequency of contractions of cardiomyocytes. The chick embryo heart explants placed on a network of elastic glass fibers continued beating for months, recorded and analyzed with the methods of computer-assisted image analysis. The efficacy of this experimental model for the screening of effects of various agents on the frequency of contractions was examined by following the effects of nifedipine, caffeine, ethanol, and benzamide. The reversibility of the effects and the reproducibility of results were demonstrated quantitatively. The significance of a mechanical elastic load provided by glass fibers for the preservation of long-lasting contractile activity of cardiomyocytes is discussed and the common occurrence of oscillatory contraction processes in various eucaryotic cells is noted.


Asunto(s)
Corazón/fisiología , Modelos Biológicos , Contracción Muscular/fisiología , Periodicidad , Animales , Benzamidas/farmacología , Cafeína/farmacología , Fármacos del Sistema Nervioso Central/farmacología , Embrión de Pollo , Evaluación Preclínica de Medicamentos , Etanol/farmacología , Corazón/efectos de los fármacos , Corazón/embriología , Técnicas In Vitro , Contracción Muscular/efectos de los fármacos , Miocardio/citología , Reproducibilidad de los Resultados
18.
Acta Haematol Pol ; 26(3): 315-9, 1995.
Artículo en Polaco | MEDLINE | ID: mdl-8525779

RESUMEN

51 years old male with acute lymphoblastic leukaemia in hematological remission was admitted to the hospital due to abrupt loss of vision. The cause of estimated complication was symmetrical infiltration of optical nerves. No other symptoms of leukaemia were observed at the time. In spite of combined radio- and chemotherapy no improvement was achieved. Two months later leukaemia relapse in the bone marrow was observed. The patient died of septic complications during reinduction treatment.


Asunto(s)
Neoplasias de los Nervios Craneales/diagnóstico , Enfermedades del Nervio Óptico/diagnóstico , Leucemia-Linfoma Linfoblástico de Células Precursoras/diagnóstico , Neoplasias de la Médula Ósea/patología , Resultado Fatal , Humanos , Masculino , Persona de Mediana Edad , Recurrencia
19.
Folia Histochem Cytobiol ; 32(2): 113-8, 1994.
Artículo en Inglés | MEDLINE | ID: mdl-7958069

RESUMEN

The experiments on the effect of various sera and substratum surface area upon growth of chick embryo fibroblast-like cells in secondary cultures are described and discussed on the grounds of a mathematical model for growth of anchorage-dependent cells proposed by Frame and Hu [14]. The model and presented results demonstrate the mutual independence of the effects of agents influencing the rate of cell proliferation (i.e. accelerating or retarding growth) and the agents that modify the limitation of cell proliferation (i.e. maximum cell density at confluence). The model proposed by Frame and Hu due to its relative simplicity offers an easy mode of description and quantitative evaluation of experiments concerning cell growth regulation. It is shown that various sera added at constant concentration significantly modify the rate of cell proliferation with little effect upon the maximum cell density attainable. The cells grew much more slowly in the presence of calf serum than in the presence of chick serum and the addition of iron and zinc complexes to calf serum significantly accelerated cell growth. An increase in the substratum surface area by the addition of glass wool to culture vessels significantly increased cell density per constant volume of medium even when retardation of growth was observed. The results presented point to the need of direct cell counting for estimation of cell growth curves and discussion of effects of agents influencing parameters characterizing cell proliferation.


Asunto(s)
Factores de Crecimiento de Fibroblastos/análisis , Fibroblastos/efectos de los fármacos , Aneuploidia , Animales , División Celular/efectos de los fármacos , Embrión de Pollo , Medios de Cultivo , ADN/biosíntesis , Factores de Crecimiento de Fibroblastos/farmacología , Cinética , Modelos Biológicos , Timidina/metabolismo
20.
Acta Haematol Pol ; 20(2): 195-200, 1989.
Artículo en Polaco | MEDLINE | ID: mdl-2638538

RESUMEN

The authors present clinical analysis of 57 patients with chronic lymphocytic leukaemia, observed during the first three stages of the disease according to Rai classification. The analysis of the presented material has confirmed the clinical and prognostic value of this classification, but at the same time has shown differences of clinical course of the disease in particular patient. There was no sex neither age effect on the clinical course of chronic lymphocytic leukemia. The authors confirmed that leukocyte doubling time is a very useful prognostic factor in chronic lymphocytic leukaemia.


Asunto(s)
Leucemia Linfocítica Crónica de Células B/sangre , Recuento de Leucocitos , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Pronóstico
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA