Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
Mais filtros










Intervalo de ano de publicação
1.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-782081

RESUMO

0.05). Similarly, no significant difference was detected in retinal arteriolar tortuosity (Z=0.91) and venular tortuosity (Z=1.31) (both p>0.05). However, the retinal arteriolar FD (mean difference: −0.03, 95% CI: −0.05, −0.01) and venular FD (mean difference: −0.03, 95% CI: −0.05, −0.02) were associated with cognitive impairment.CONCLUSIONS: A smaller retinal microvascular FD might be associated with cognitive impairment. Further large-sample and well-controlled original studies are required to confirm the present findings.


Assuntos
Transtornos Cognitivos , Fractais , Viés de Publicação , Retina , Artéria Retiniana , Vasos Retinianos , Retinaldeído
2.
Chinese Pharmacological Bulletin ; (12): 1045-1048,1049, 2014.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-599534

RESUMO

Intestinal microflora is an important part of the organ-ism, promoting digestion and absorption of nutrients, maintaining intestinal normal physiological function, regulating immune sys-tem. Intestinal microflora maintains steady state under normal conditions, but intestinal microbiota dysbiosis occurs when surrounding environment c hanges, such as age, diet, obesity and other metabolic diseases as well as antibiotics. Many recent studies have found intestinal flora could cause a variety of disea-ses, and colon cancer is closely related with intestinal microbiota dysbiosis. Some researches suggest improving the intestinal flora dysbiosis can reduce the incidence of colon cancer and inhibit the growth and the worsening of colon cancer. However, under-lying mechanisms remain unknown. So this article summarizes the research progress on the development of colon cancer and in-testinal microbiota dysbiosis, in order to provide reference for re-search on intestinal flora and colon cancer treatment.

3.
Biomed Pharmacother ; 66(2): 89-97, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22301433

RESUMO

Recent studies have indicated that side population (SP) cells, which are an enriched source of cancer stem cells (CSCs), drive and maintain many types of human malignancies. SP cells have distinguishing biological characteristics and are thought to contribute to metastasis, therapy resistance, and tumor recurrence. In the present study, the miRNA expression profiles of SP cells and non-SP cells were compared using miRNA array analysis. Both let-7 and miR-31 were significantly down-regulated in SP cells compared to non-SP cells. The results were confirmed by real-time PCR. Engineered repression of miR-31 caused marked repression of both lung cancer SP cell and non-SP cell growth in vitro. In contrast, engineered repression of let-7 caused marked promotion of both lung cancer SP and non-SP cells growth in vitro. Cell cycle studies further revealed that reduced miR-31 could inhibit SP cell proliferation by a cell cycle arrest in the G0/G1 phase, whereas reduced let-7 induced SP cell proliferation by accelerating G1/S phase transition. Notably, reduced miR-31 prevented SP cell differentiation, whereas reduced let-7 promoted SP cell differentiation under differentiation conditions. These findings indicate that reduced miR-31 and let-7 are involved in maintaining the balance between differentiation and quiescence in SP cells.


Assuntos
Neoplasias Pulmonares/genética , MicroRNAs/genética , Células da Side Population/metabolismo , Pontos de Checagem do Ciclo Celular/genética , Diferenciação Celular/genética , Linhagem Celular Tumoral , Proliferação de Células , Regulação para Baixo , Humanos , Neoplasias Pulmonares/metabolismo , Células-Tronco Neoplásicas/metabolismo , Reação em Cadeia da Polimerase
4.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-427174

RESUMO

Objective To investigate the regulatory effects of PTEN-PI3K/AKT pathway on the apoptosis of gastric cancer MKN28 cells and the possible mechanisms.Methods The specific sequence of PTEN was transfected to MKN28 cells by eukaryotic expression vector (transfection group),and then vacant vector (negative control group) and PBS (blank control group) were transfected to the MKN28 cells,respectively.The effects of PTEN-PI3K/AKT pathway on the apoptosis of MKN28 cells and the expressions of PI3K,AKT,Caspase-3 and Caspase-9 were investigated.The growth curve and apoptosis of the MKN28 cells were detected by MTT assay and TUNEL staining,respectively,and the protein expression was detected by the Western blot.MKN28 cells which did not transfected by the PTEN were processed by inhibitor of PI3K (LY294002) (treated group),and MKN28 cells in the control group were processed by PBS.The expressions of apoptosis protein and apoptosis-related protein were detected after inhibition of PI3 K.All data were analyzed using the t test.Results The model of over-expression of PTEN was obtained and transfected into MKN28 cells.The survival of MKN28 cells in the transfection group was significantly inhibited in a time-dependant manner ( r =0.938,P < 0.05 ).The mean apoptotic rate of the transfection rate was 27.86% ± 4.78%,which was significantly higher than 0.01% ± 0.01% of the negative control group ( t =9.527,P < 0.05 ).The protein expression of PI3K in the transfection group was 0.25 ± 0.03,which was significantly lower than 0.93 ± 0.16 of the blank control group and 0.96 ± 0.15 of the negative control group (t =7.235,8.883,P < 0.05 ).The protein expression of P-AKT in the transfection group was 0.21 ± 0.03,which was significantly lower than 0.93 ± 0.13 of the blank control group and 0.91 ± 0.12 of the negative control group (t =9.347,9.802,P < 0.05 ).The expressions of Caspase-3 and Caspase-9 of the transfection group were 0.86 ± 0.11 and 0.87 ± 0.12,which were significantly higher than 0.16 ± 0.03 and 0.18 ± 0.04 of the negative control group,and 0.15 ± 0.02 and 0.16 ± 0.03 of the blank control group ( t =10.634,10.999,9.448,9.942,P <0.05).The apoptotic rate of the MKN28 cells of the treated group was 28.60% ± 4.50%,which was significantly higher than 0.12% ± 0.06% of the control group (t =10.961,P < 0.05 ).The protein expression of PI3K and P-AKT of the treated group were 0.18 ± 0.02 and 0.11 ± 0.01,which were significantly lower than 0.93 ± 0.14 and 0.90 ± 0.12 of the control group (t =9.186,11.363,P < 0.05 ).The protein expression of PTEN of the treated group was 1.15 ± 0.15,which was significantly higher than 0.21 ± 0.08 of the control group (t =9.577,P < 0.05 ).The relative expressions of Caspase-3 and Caspase-9 of the treated group were 0.86 ± 0.12 and 0.88 ± 0.11,which were significantly higher than 0.25 ± 0.02 and 0.21 ± 0.03 of the control group (t =8.685,10.178,P < 0.05).Conclusions Over-expression of PTEN may enhance the apoptosis of gastric cancer cells through inhibition of PI3K/AKT pathway.Inhibition of PI3K can enhance the expression of PTEN.PI3K and PTEN regulate the apoptosis of gastric cancer cells.

5.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-521809

RESUMO

Objective To investigate the effect of transforming growth factor ?1 on secretion function of rat islet allograft in vivo and in vitro.Methods Expressing vector of rat TGF-?1 was constructed and transfected to purify Wistar rat islets. Expression of TGF-?1 and rat insulin1 gene (Ins1) in experiment and control group was detected by RT-PCR; Streptozotocin 60mg/kg intra-abdominal injection prepared the SD rat diabetic model. Insulin of cultured islets at basal and stimulated phase in vitro was detected by RIA; Islet allotransplantation was performed under recipient SD rats' renal subcapsule. The level of blood glucose was recorded before and after transplantation. The glucose tolerance was also tested.Results Expression of both TGF-?1 and Ins1 were detected in experimental group, but only Ins1 was detected in control one; Experiment and control islets secreted 3 86?1 24ng/mL and 4 13?1 45ng/mL at basal phase, 8 43?1 59ng/mL and 8 95?1 74ng/mL at stimulating phase, respectively.No significant difference was observed between two groups, but it was in groups. Experimental group' mean normal glycemia value (26 8?2 9) days was significantly longer that control group (13 2?4 5 days). Control group's glucose tolerance curve was significantly above experiment one's.Conclusion TGF-?1 can prolong the survival of islet allograft while it does not impair graft's endocrine function.

6.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-674957

RESUMO

0.05) while those between GCT Ⅰ and the collection of GCT Ⅱ and GCT Ⅲ were significant ( P 0.05).Conclusion:The results indicated that neither the p16 positive rate nor the p27 positive rate could be used independently for defining grade of malignancy and estimating prognosis of malignant bone tumors though p16 and p27 might play important roles in the genesis of bone tumors.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...