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1.
Journal of Regional Anatomy and Operative Surgery ; (6): 10-15, 2019.
Article in Chinese | WPRIM | ID: wpr-744539

ABSTRACT

Objective To investigate the role of microRNA-10b (miR-10b) in the proliferation and invasion potential of osteosarcoma cell lines MG-63 and the exact underlying mechanism.Methods The expression level of miR-10b in human osteosarcoma tissue samples and adjacent normal bone tissues were detected by relative quantitative real-time PCR (qRT-PCR).miR-10b mimic and siRNA against Twist (Twist siRNA) were transfected into human osteosarcoma cell lines MG-63 respectively using lipofactamine 2000, and RT-PCR was used to detect the mRNA expression levels of miR-10b and Twist, and Twist protein expression level was detected by Western blot.The effect of miR-10b mimic and Twist siRNA on proliferation of MG-63 were detected by MTT[3- (4, 5-dimethylthiazol-2-yl) -5- (3-carboxymethoxyphenyl) -2- (4-sulfophenyl) -2 H-tetrazolium].The in-vitro cell invasion ability was determined by Transwell invasion assays after up-regulating miR-10b or knocking down of Twist.Results The expression levels of miR-10b was higher in human osteosarcoma tissue samples compared with adjacent normal bone tissues, the differences were extremely statistical significance (P<0.01).miR-10b directly up regulated the mRNA and protein expression levels of Twist, the differences were significant (P<0.05).In addition, miR-10b had enhanced the cell invasion and the proliferation (P<0.05), whereas the proliferation and invasion ability of MG-63 which transfected by both miR-10b mimic and Twist siRNA were significantly reduced than that transfected by miR-10b mimic (P<0.05).Conclusion miR-10b in MG-63 promotes the proliferation and invasion potential of human osteosarcoma cell lines MG-63, at least partly through the upregulation of Twist gene.

2.
Chinese Journal of Clinical and Experimental Pathology ; (12): 10-13, 2019.
Article in Chinese | WPRIM | ID: wpr-743331

ABSTRACT

Purpose To detect the expression of N-Myc and p53 in the tissues of prostate cancer (PCa) patients and to explore the relationship between them and their significance.Methods A total of 63 patients with PCa and 50 patients with benign prostatic hyperplasia (BPH) who underwent prostate surgery at the First Affiliated Hospital of Anhui Medical University were recruited in 2015-2016. The expression of N-Myc and p53 in pathological tissues were detected by immunohistochemistry of MaxVision method. Results The expression of N-Myc and p53 in PCa tissues was increased (P < 0.05). The expression of N-Myc and p53 in PCa tissues was correlated with bone metastases and TNM stage (P < 0.05), but not related to patient age, preoperative PSA level and other factors (P> 0.05). In addition, the expression of p53 was also correlated with Gleason score.Conclusion The high expression of N-Myc and p53 in PCa may involved in the malignant progression and metastasis of prostate cancer, and it is expected to become a new target for detecting PCa metastasis.

3.
China Journal of Chinese Materia Medica ; (24): 2807-2813, 2015.
Article in Chinese | WPRIM | ID: wpr-337886

ABSTRACT

WRKY transcription factors are novel transcriptional regulatory factors, which play an important role in regulating plant development, metabolism and other physiological processes. In this study, a new Dendrobium officinale WRKY transcription factor, designated as DoWRKY1 was cloned by using RT-PCR and RACE (GenBank Accession No. KF953910). Bioinformatic analysis demonstrated that, the full-length cDNA of DoWRKY1 was 1,704 bp. And DoWRKY1 contained a 1,629 bp open reading frame (ORF) that encoding a peptide of 542 amino acid residues. The putative DoWRKY1 protein contained two conserved WRKY domains and it belonged to the group I WRKY family protein. Yeast one-hybrid experiment showed that DoWRKY1 had transcriptional activation ability in yeast, and it could activate the expression of downstream report genes (His3 and Ade2). Semi-quantitative RT-PCR experiment showed that DoWRKY1 expressed in roots, stems, leaves and protocorm-like bodies. Real-time qRT-PCR proved that DoWRKY1 could be induced by methyl jasmonate (MeJA) and chitosan (Chitosan), and the expression level of this gene can reach the expression peak at 2 h and 1 h, respectively. These results are useful for further determination of the regulation function of this gene in secondary metabolism of D. officinale.


Subject(s)
Cloning, Molecular , Dendrobium , Genetics , Gene Expression Regulation, Plant , Plant Proteins , Genetics , Transcription Factors , Genetics
4.
China Journal of Chinese Materia Medica ; (24): 6-10, 2008.
Article in Chinese | WPRIM | ID: wpr-324311

ABSTRACT

<p><b>OBJECTIVE</b>To study the genetic diversity of medicinal Dendrobium by SRAP.</p><p><b>METHOD</b>The genetic diversity of 9 spices Dendrobium was studied by using the optimized SRAP reaction system. The NTSYS software was used to analyze the markers.</p><p><b>RESULT</b>Forty primer pairs were selected from 88 amplified 1 782 polymorphic bands with an average of 44.55 polymorphic bands per primer pair. Cluster analysis using UPGMA method based on the data of SRAP amplified bands by 40 primer pairs showed that 9 spices of could be distinguished into two main groups. Jaccard's similarity coefficient ranged from 0.330 2-0.789 2.</p><p><b>CONCLUSION</b>The results of this research indicate that SRAP molecular marker is efficient to study the medical Dendrobium genetic diversity.</p>


Subject(s)
Dendrobium , Classification , Genetics , Genetic Variation , Genetics , Nucleic Acid Amplification Techniques , Methods , Phylogeny , Plants, Medicinal , Classification , Genetics , Polymerase Chain Reaction
5.
China Journal of Chinese Materia Medica ; (24): 1401-1404, 2006.
Article in Chinese | WPRIM | ID: wpr-316039

ABSTRACT

<p><b>OBJECTIVE</b>To compare the hybrid between species of Dendrobium huoshanense and its parents on growing, physiologic indexes and content of medicinal components, and provide theoretical basis for species quality improvement.</p><p><b>METHOD</b>The chlorophyll content, the photosynthesis rate, the polysaccharides content and the alkaloids content were measured by anhydrous ethanol method, Cl-310 photosynthesis determination system, colorimetry of concentrated sulphuric acid-phenol and acid dyes colorimetry respectively.</p><p><b>RESULT</b>The growth of hybrid was close to D. moniliforme, and apparently higher than D. huoshanense. The chlorophyll content and the photosynthesis rate of one-year-hybrid were markedly higher than its parents. The content of polysaccharides and alkaloids in two-year-stem and three-year-stem of hybrid were close to that of D. huoshanense.</p><p><b>CONCLUSION</b>The hybrid integrates superiority of parents on growth and accumulation of medicinal components opens vast vistas for development and utilization.</p>


Subject(s)
Alkaloids , Chlorophyll , Dendrobium , Chemistry , Classification , Genetics , Hybridization, Genetic , Photosynthesis , Plants, Medicinal , Chemistry , Classification , Genetics , Polysaccharides
6.
China Journal of Chinese Materia Medica ; (24): 1064-1068, 2005.
Article in Chinese | WPRIM | ID: wpr-358030

ABSTRACT

<p><b>OBJECTIVE</b>Through a comparison between F1 and its' parents on the growth, chemical components and physiology, this study aims to find the possibility of selecting new dendrobium hybrids with high yield and good quality.</p><p><b>METHOD</b>To determinate the growth, chemical components, photosynthesis, hormones and isoenzyme in the plants.</p><p><b>RESULT</b>Photosynthetic area, content of chlorophyll, net photosynthesis and yield of F1 generation are higher than those of the parents; chla/b rate is lower; growth is almost the same as in Dendrobium moniliforme; content of chemical components are the same as in D. huoshanense. F1 is approaching of advantages of parents.</p><p><b>CONCLUSION</b>Physiological characters, yield and quality of F1 are greatly improved by hybridization.</p>


Subject(s)
Alkaloids , Chlorophyll , Dendrobium , Chemistry , Classification , Genetics , Hybridization, Genetic , Photosynthesis , Plant Growth Regulators , Plant Proteins , Plants, Medicinal , Chemistry , Classification , Genetics , Polysaccharides
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