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1.
Cell Biochem Biophys ; 71(2): 1255-9, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25424357

RESUMO

This study was set to determine the expression of microRNA-449a in cancer tissue and serum of non-small cell lung cancer (NSCLC) patients and explore the underlying mechanisms of its tumor suppressor functions. We selected 50 NSCLC patients in our hospital as the lung cancer group and 50 healthy volunteers as the control group. RT-PCR was performed to detect the expression levels of microRNA-449a in NSCLC tissue and the plasma of NSCLC patients. Further, we transfected microRNA-449a mimic and inhibitor in lung cancer cell line A549, and used western blot to determine the expression level of apoptosis-related molecules Bcl-2 and p53. Compared with the surrounding tissue, microRNA-449a exhibited significantly reduced mRNA expression, which was statistically different (P < 0.05). microRNA-449a exhibited significantly lower expression in NSCLC patients' plasma than the healthy volunteers, which was statistically different (P < 0.05). Spearman correlation analysis showed that microRNA-449a expression levels in NSCLC tissue and plasma of NSCLC patients were reversely correlated with lung cancer differentiation (P < 0.05). But microRNA-449a expression in the surrounding tissue was not significantly correlated with lung cancer differentiation (P > 0.05). Compared with negative control, cell proliferation and p53 and Bcl-2 expression significantly decreased after microRNA-449a mimic transfection (P < 0.05). However, after transfection of microRNA-449a inhibitor, cell proliferation and p53 and Bcl-2 expression significantly increased after microRNA-449a mimic transfection (P < 0.05). microRNA-449a expression levels in NSCLC are significantly lower than those in the surrounding tissue, and its expression levels in NSCLC patients are also lower than those in healthy volunteers. The tumor suppression role of microRNA-449a could be due to its promotion of tumor cell proliferation and its inhibition of tumor cell apoptosis.


Assuntos
Apoptose/genética , Carcinoma Pulmonar de Células não Pequenas/genética , Carcinoma Pulmonar de Células não Pequenas/patologia , Neoplasias Pulmonares/genética , MicroRNAs/genética , Linhagem Celular Tumoral , Humanos
2.
J Food Drug Anal ; 22(4): 431-438, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-28911457

RESUMO

The volatile and odor-active compounds in cooked meat of farmed obscure puffer (Takifugu obscurus) were analyzed by gas chromatography-mass spectrometry-olfactometry (GC-MS-O). The volatile compounds were extracted by the simultaneous distillation-extraction (SDE) method, then separated and identified by GC-MS. Odor-active compounds in the SDE extract were characterized by GC-MS-O. A total of 68 volatile compounds were found, including 23 aldehydes, 10 alcohols, nine ketones, 17 N- or S-containing compounds and aromatics, three acids, three alkanes, and three esters. Of these, 31 odor-active compounds were detected and identified. Trimethylamine (fishy), octanal (grassy, leafy, green), (E)-2-octenal (roast, fatty), 1-octen-3-ol (fishy, fatty, mushroom, grassy), 2-ethyl-1-hexanethiol (cooked fish), (E,E)-2,4-octadienal (cooked meat, sweet), 2-acetylthiazole (meaty, roast, nutty, sulfur), 2-acetylpyrrole (nutty, walnut, bread) were identified as the key odorants in the cooked meat of farmed obscure puffer based on posterior intensity and time-intensity methods.

3.
Yao Xue Xue Bao ; 39(1): 37-40, 2004 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-15127579

RESUMO

AIM: To study the synthesis of 5-(3'-indolyl)-oxazoles and their antioxidative activity. METHODS: The amides were prepared from tryptophan and different acid derivatives by the catalytic dehydration of dicyclohexyl carbodiimide (DCC). The characteristic heterocyclic ring system of 5-(3'-indolyl)-oxazoles was constructed by oxidative cyclization of amide, using dicholorodicyanoquinone (DDQ). Their antioxidative activity in vitro was tested using DPPH system. RESULTS: Eleven 2-substituted phenyl-5-(3'-indolyl)-oxazoles were prepared, the compounds 21 and 22 have shown antioxidative activity 3-4 times stronger than that of Vit E, and the compound 29 showed antioxidative activity almost as same as Vit E. CONCLUSION: Three 5-(3'-indoyl)-oxazole compounds synthesized showed potent antioxidative effect and they would be a good antioxidants.


Assuntos
Antioxidantes/síntese química , Indóis/isolamento & purificação , Oxazóis/isolamento & purificação , Antioxidantes/química , Indóis/química , Estrutura Molecular , Oxazóis/química
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