Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Mais filtros

Base de dados
País/Região como assunto
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Cancer Sci ; 108(3): 408-418, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28370854

RESUMO

microRNAs play key roles during various crucial cell processes such as proliferation, migration, invasion and apoptosis. Also, microRNAs have been shown to possess oncogenic and tumor-suppressive functions in human cancers. Here, we describe the regulation and function of miR-149 in colorectal cancer cell lines. miR-149 expression patterns were detected in human colorectal cell lines and tissue samples, and then focused on its role in regulation of cell growth, migration, invasion, and its target gene identification. Furthermore, the function of the target gene of miR-149 was analyzed in vitro and in vivo. miR-149 expression was downregulated in human colorectal cancer HCT116 and SW620 cell lines compared to the normal colon epithelial NCM460 cell line using quantitative real-time polymerase chain reaction methods. Further studies indicated that introduction of miR-149 was able to suppress cell migration and invasion. Then, EphB3 was identified as a direct target gene of miR-149 in colorectal cancer cells. Moreover, experiments in vitro showed that knockdown expression of EphB3 could suppress cell proliferation and invasion, and ectopic expression of EphB3 restored the phenotypes of CRC cell lines transfected with miR149. In addition, silencing of EphB3 significantly affected cycle progression distribution and increased apoptosis in CRC cell lines. Finally, in vivo results demonstrated that knockdown of EphB3 by siRNA inhibited tumor growth. In conclusion,the important role of miR-149 in colorectal cancer progression suggesting that miR-149 may serve as a therapeutic target for colorectal cancer treatment.


Assuntos
Movimento Celular/genética , Proliferação de Células/genética , Neoplasias do Colo/patologia , Regulação Neoplásica da Expressão Gênica , MicroRNAs/genética , Receptor EphB3/metabolismo , Animais , Apoptose/genética , Linhagem Celular Tumoral , Neoplasias do Colo/genética , Regulação para Baixo , Feminino , Células HCT116 , Humanos , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Nus , Invasividade Neoplásica/genética , Transplante de Neoplasias , Interferência de RNA , RNA Interferente Pequeno/genética , Reação em Cadeia da Polimerase em Tempo Real , Receptor EphB3/genética , Transplante Heterólogo
2.
Environ Sci Pollut Res Int ; 30(50): 109007-109020, 2023 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-37759047

RESUMO

This study investigates the feasibility of using renewable energy sources in soil remediation to advance green recovery in a way that is both sustainable and kind to the environment. The report stresses the need to reduce the adverse effects of soil pollution in China and foster economic recovery. This study aims to determine how green energy may be most effectively used in soil remediation operations. Using renewable energy sources to power remediation procedures and phytoremediation is presented in this research as two ways to achieve green recovery in soil remediation. The analysis in this work employs the unit root, auto-regressive distributive lag (ARDL), and vector error correction model (VECM) methods. Based on our research, we know that using renewable energy sources like solar, wind, and geothermal power may significantly lessen the environmental impact of soil remediation while simultaneously advancing the cause of sustainability. Phytoremediation is a low-cost, environmentally friendly option that utilizes plants to degrade and remove soil pollutants. The study's findings also stressed the need to consider various remediation strategies' advantages and disadvantages. The study's findings also exposed the potential advantages and disadvantages of phytoremediation, as was the method's viability for use in extensive soil remediation initiatives. The report concludes by emphasizing the need to assess soil remediation and green recovery's more enormous social and environmental implications. We can build a more sustainable future, encourage economic recovery, and combat environmental degradation using renewable energy sources and cutting-edge remediation techniques. The article suggests doing more studies to learn more about the pros and downsides of combining soil remediation and green recovery initiatives.


Assuntos
Poluentes do Solo , Solo , Biodegradação Ambiental , Poluentes do Solo/análise , Plantas/metabolismo , China , Energia Renovável
4.
Biomed Pharmacother ; 108: 1775-1782, 2018 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-30372881

RESUMO

Increasing evidence suggests the involvement of long non-coding RNAs (lncRNAs) in chemoresistance of cancer treatment. However, their function and molecular mechanisms in gastric cancer chemoresistance are still not well elucidated. In the present study, we investigate the functional role of lncRNA cancer susceptibility candidate 2 (CASC2) in cisplatin (DDP) resistance of gastric cancer and discover the underlying molecular mechanism. Results revealed that CASC2 was decreased in DDP-resistant gastric cancer tissues and cells. Gastric cancer patients with low CASC2 expression levels had a poor prognosis. CASC2 overexpression enhanced DDP sensitivity of BGC823/DDP and SGC7901/DDP cells. Conversely, CASC2 knockdown weakened the response of BGC823 and SGC7901 to DPP. Moreover, CASC2 could function as a miR-19a sponge. miR-19a inhibition could overcome DDP resistance in BGC823/DDP and SGC7901/DDP cells, while miR-19a overexpression led to DDP resistance in BGC823 and SGC7901 cells. Notably, miR-19a overexpression counteracted CASC2 up-regulation-mediated enhancement in DDP sensitivity of BGC823/DDP and SGC7901/DDP cells. On the contrary, the inhibitory effect of CASC2 knockdown on the sensitivity of BGC823 and SGC7901 cells to DDP was reversed by miR-19a inhibition. In summary, CASC2 overexpression overcame DDP resistance in gastric cancer by sponging miR-19a, providing a novel therapeutic target for gastric cancer chemoresistance.


Assuntos
Cisplatino/farmacologia , Regulação para Baixo/genética , Resistencia a Medicamentos Antineoplásicos/genética , MicroRNAs/metabolismo , Neoplasias Gástricas/genética , Proteínas Supressoras de Tumor/genética , Sequência de Bases , Linhagem Celular Tumoral , Regulação para Baixo/efeitos dos fármacos , Resistencia a Medicamentos Antineoplásicos/efeitos dos fármacos , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Humanos , MicroRNAs/genética , Proteínas Supressoras de Tumor/metabolismo
5.
J Acupunct Meridian Stud ; 10(4): 252-260, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28889842

RESUMO

Allergic contact dermatitis (ACD) is a chronic inflammatory skin disease. Topical corticosteroids are the first-line therapy for ACD despite their significant adverse effects. Acupuncture has been widely used in the treatment of various skin diseases, but its underlying mechanism remains unrevealed. In this study, we investigated the characteristics of acupuncture treatment based on effectiveness and mechanism. BALB/c mice received 1-chloro-2,4-dinitrobenzene (DNCB) application to build AD-like model. Results showed that acupuncture was an effective treatment method in inhibiting inflammatory conditions, serum IgE levels, and expression of proinflammatory cytokine Th2 (IL-4, IL-6), and Th2 (IL-1ß, TNF-α) mRNA compared with DNCB treatment. Acupuncture treatment also inhibited nuclear factor-κB p65, phosphorylation of IκBα, and phosphorylation of occludin proteins expression. Furthermore, it could improve the expression of epidermal growth factor in both mRNA and protein levels. These results suggest that acupuncture, as an alternative therapy treatment for its no significant side effects, was effective in alleviating ACD by reducing proinflammatory cytokines and changing proteins' expression.


Assuntos
Terapia por Acupuntura , Dermatite Alérgica de Contato/terapia , Animais , Citocinas/análise , Citocinas/metabolismo , Dermatite Alérgica de Contato/imunologia , Dermatite Alérgica de Contato/patologia , Dermatite Alérgica de Contato/fisiopatologia , Dinitroclorobenzeno/efeitos adversos , Modelos Animais de Doenças , Fator de Crescimento Epidérmico/análise , Fator de Crescimento Epidérmico/metabolismo , Feminino , Imunoglobulina E/análise , Camundongos , Camundongos Endogâmicos BALB C , Ocludina/análise , Ocludina/metabolismo , Pele/química , Pele/efeitos dos fármacos , Pele/patologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA