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Chinese Journal of Integrated Traditional and Western Medicine ; (12): 167-173, 2015.
Artigo em Chinês | WPRIM | ID: wpr-297460

RESUMO

<p><b>OBJECTIVE</b>To explore the effect of Jianpi Tongluo Jiedu Recipe (JTJR) on protein expression levels of COX-2, NF-kappaBp65, Bcl-2, and Bax, mRNA expression levels of COX-2 and Bcl-2, and the apoptotic index (Al) in gastric mucosa of patients with precancerous lesions of gastric cancer (PL-GC).</p><p><b>METHODS</b>Totally 65 PLGC patients were recruited and treated by JTJR (modified by syndrome typing), one dose per day for six successive months. Protein expression levels of COX-2, NF-KBp65, Bcl-2, and Bax were detected in 65 patients using immunohistochemical (IHC) assay before and after treatment. mRNA expression levels of COX-2 and Bcl-2 were detected in 54 patients using reverse transcription-polymerase chain reaction (RT-PCR). Meanwhile, changes of Al was detected in 65 patients using TdT-mediated dUTP-biotin nick end labeling (TUNEL) fluorescence method.</p><p><b>RESULTS</b>After treatment with JTJR, positive protein expression levels of COX-2, NF-KBp65, and Bcl-2 were obviously decreased in the gastric mucosa of PLGC patients (P <0.01), but Bax positive protein expression was found to be higher (P < 0.05). At the same time mRNA expression levels of COX-2 and Bcl-2 were significantly lower after treatment than before treatment (P < 0.05, P < 0.01); Al also increased after treatment (P < 0.05).</p><p><b>CONCLUSION</b>JTJR could promote apoptosis possibly via NF-kappaBp65/COX-2, COX-2/Bcl-2, and NF-kappaBp65/Bcl-2 signaling pathways, thereby affecting PLGC patients.</p>


Assuntos
Humanos , Apoptose , Ciclo-Oxigenase 2 , Metabolismo , Medicamentos de Ervas Chinesas , Farmacologia , Usos Terapêuticos , Mucosa Gástrica , Metabolismo , NF-kappa B , Metabolismo , Lesões Pré-Cancerosas , Tratamento Farmacológico , Metabolismo , Proteínas Proto-Oncogênicas c-bcl-2 , Metabolismo , Transdução de Sinais , Neoplasias Gástricas , Tratamento Farmacológico , Metabolismo , Proteína X Associada a bcl-2 , Metabolismo
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