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1.
China Journal of Chinese Materia Medica ; (24): 4055-4061, 2018.
Article in Chinese | WPRIM | ID: wpr-775379

ABSTRACT

This research preliminarily discusses the relations of Dendrobium system growth through chloroplast gene rbcL, matK and the nuclear genome ITS2. The DNA barcoding universal sequence for authentication of the Dendrobium medical plants was slected and the possibility concerning utilizing the DNA barcoding to distinguish the D. huoshanenseand its adulterants was analyzed. Using the universal primer pair of ITS2, rbcL and matK, series of extended sequencing in the Dendrobium were conducted. Meanwhile, considering the different index about amplification and sequencing success rate of each sequence, the intraspecific and interspecific aberrance, the employment of BioEdit and MEGA 5.0 software were applied to establish the systematic tree of the NJ molecular and evaluate the diversified authentication capability of various sequences. The consequence demonstrates that the sequence of ITS2 is not only the largest one both in the intraspecific and interspecific aberrance of the Dendrobium but also has obvious barcoding gap. Considering the few overlap between the intraspecific and interspecific aberrance and the highest percentage regarding the formation of unilateral branch in diverse Dendrobium which have different ITS2 sequences, it can differentiate the species of Dendrobium. Furthermore, due to the inferior success rate of the rbcL and thematK and the lower reliability of NJ systematic tree, the percentage of the unilateral species which are generated by the systematic tree of rbcL and matK sequences is deficient. Therefore, the sequence of ITS2 can serves as DNA barcoding to distinguish the D. huoshanense, the D. moniliform and the D. officinale.


Subject(s)
DNA Barcoding, Taxonomic , DNA, Plant , Genetics , Dendrobium , Classification , Drug Contamination , Plant Preparations , Reference Standards , Plants, Medicinal , Classification , Reproducibility of Results
2.
Journal of Experimental Hematology ; (6): 477-483, 2018.
Article in Chinese | WPRIM | ID: wpr-690963

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of bortezomib(BTZ) and thalidomide(TM) on peripheral blood memory T-cells (T) and regulatory T cells(Tregs) in patients with multiple myeloma(MM).</p><p><b>METHODS</b>Eighty-six MM patients received 2 courses of chemotherapy were divided into effective (partial response at least) group (63 cases) and ineffective (no partial response) group (17 cases) according to therapeutic efficacy; these 80 patients were divided into BTZ group (38 cases) and TM group (42 cases) yet according to therapeutic regimens, 20 newly diagnosed MM patients were used as baseline group, 30 healthy volunteers were used as healthy control group. The T subsets and Treg in peripheral blood of each groups were detected by flow cytometry.</p><p><b>RESULTS</b>The CD4 central memory T cells (CD4 T) percentage of CD4 T, the CD18 T percentage of CD18T and ratio of CD8 T and CD8 effector memory T cells (T) (CD8 T/T) in baseline group were all significantly lower than those in healthy control group (P<0.05). After treatment with BTZ regimen or TM regimen, the CD8T percentage of CD8 T in effective group significantly increased to level of healthy control group (P<0.05); the Treg cell level in effective and in effective groups was not significantly different from that in baseline group(P>0.05), but the Treg percentage of CD4 cells ineffective group was significantly higher than that in baseline group and ineffective group (P<0.05). According to ROC curve, the critical value of CD8T/T for predicting chemotherapeutic response was 0.27 with sensitivity of 57.1% and specificity of 94.1%.</p><p><b>CONCLUSION</b>When MM patients are in an immuno-exhanstive status, the treatment with BTZ or TM both can reverse the immuno-inhibitory status of MM patients, moreover, does not affect the Treg cell count; the Treg percentage in BTZ and TM effective groups both are significantly higher than that in baseline group and ineffective group. The ratio of CD8T/T contributes to evaluating the chemotherapeutic efficacy.</p>


Subject(s)
Humans , Bortezomib , Flow Cytometry , Multiple Myeloma , T-Lymphocyte Subsets , T-Lymphocytes, Regulatory , Thalidomide
3.
Chinese Journal of Current Advances in General Surgery ; (4): 515-517,521, 2017.
Article in Chinese | WPRIM | ID: wpr-660395

ABSTRACT

Objective:To investigate the role of Notch signaling pathway in the migration of hepatocellular carcinoma cells and its related mechanisms.Methods:HepG2 was cultured in vitro,which was HL-7702,Huh-7.The migration ability of Transwell cells was detected,Notch,Snail,Westernblot to detect the expression of E-cadherin protein.1 mol/L DAPT and 5 mol/L DAPT were used to block the Notch signaling pathway,and compared the effects of different concentrations on cell migration and the expression of Snail and E-cadherin protein in hepatocellular carcinoma cells.Results:The invasion and migration ability of HCC cell lines was significantly higher than that of normal non neoplastic liver cells (P<0.05).The invasion and migration ability of HepG2 was slightly higher than that of Huh-7,but the difference was not statistically significant (P>0.05).Used Western blot method to detect protein imprinting cells Notch,SnaiI,E-cadherin protein expression,results showed that the expression of Notch and Snail in liver cancer cells than normal cells,the expression of E-cadherin was significantly lower than that of normal cells.Blocking the Notch signaling pathway by 1 mol/L DAPT and 5 mol/L DAPT results showed that compared with the control group,the expression of 1 mol/L DAPT and 5 mol/L DAPT can significantly reduce Snail,increased the expression of E-cadherin,and with the increase of the concentration of strengthening effect (P<0.05).Conclusion:Notch signaling pathway plays an important role in the invasion and migration of hepatocellular carcinoma cells.It is believed that the expression of Snail and E-cadherin may be related to the expression.

4.
Chinese Journal of Current Advances in General Surgery ; (4): 515-517,521, 2017.
Article in Chinese | WPRIM | ID: wpr-657886

ABSTRACT

Objective:To investigate the role of Notch signaling pathway in the migration of hepatocellular carcinoma cells and its related mechanisms.Methods:HepG2 was cultured in vitro,which was HL-7702,Huh-7.The migration ability of Transwell cells was detected,Notch,Snail,Westernblot to detect the expression of E-cadherin protein.1 mol/L DAPT and 5 mol/L DAPT were used to block the Notch signaling pathway,and compared the effects of different concentrations on cell migration and the expression of Snail and E-cadherin protein in hepatocellular carcinoma cells.Results:The invasion and migration ability of HCC cell lines was significantly higher than that of normal non neoplastic liver cells (P<0.05).The invasion and migration ability of HepG2 was slightly higher than that of Huh-7,but the difference was not statistically significant (P>0.05).Used Western blot method to detect protein imprinting cells Notch,SnaiI,E-cadherin protein expression,results showed that the expression of Notch and Snail in liver cancer cells than normal cells,the expression of E-cadherin was significantly lower than that of normal cells.Blocking the Notch signaling pathway by 1 mol/L DAPT and 5 mol/L DAPT results showed that compared with the control group,the expression of 1 mol/L DAPT and 5 mol/L DAPT can significantly reduce Snail,increased the expression of E-cadherin,and with the increase of the concentration of strengthening effect (P<0.05).Conclusion:Notch signaling pathway plays an important role in the invasion and migration of hepatocellular carcinoma cells.It is believed that the expression of Snail and E-cadherin may be related to the expression.

5.
Journal of Experimental Hematology ; (6): 1576-1579, 2017.
Article in Chinese | WPRIM | ID: wpr-301685

ABSTRACT

Over the last decade, bortezomib(BTZ) has been extensively applied in the treatment of hematological malignancies, particularly in multiple myeloma and mantle cell lymphoma, however, the appearence of secondary resistance to BTZ has brought a huge challenge in MM treatment. In the present review, the mechanisms of resistance to bortezomib in MM are summarized, focusing on the action of ubiquitin-proteasome system(UPS), endoplasmin reticulum stress, antophagy, inducible pro-survival signalling and bone marrow microenvironment as well as exploration of the potential therapeutic strategies in the clinical perspective. With the understanding of the molecular mechanisms for resistance to BTZ, the novel histone deacetylase inhibitors(HDACi) have been approved for the treatment of replased/refractory MM and AKT inhibitor in the clinical trials. These novel combined therapies can enhance BTZ efficiency and improve the outcome of the patients.

6.
Chinese Journal of Experimental and Clinical Virology ; (6): 127-129, 2008.
Article in Chinese | WPRIM | ID: wpr-254122

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the characteristics of seroconversion of HBV NAT screening-positive crowd from blood donors in Dongguan city and provide reference for the safety of blood transfusion and disease prevention.</p><p><b>METHODS</b>With retrospective survey, Nucleic acid testing (NAT) was used to analyze 28800 HBsAg-negative samples by ELISA from blood donors in Dongguan city from August, 2006 to August, 2007 with Roche Cobas AmpliScreen systems; and follow-up research including NAT for HBV-DNA, ELISA for HBsAg and multiple factors analysis for HBV infection was carried out on HBV NAT screening-positive crowd.</p><p><b>RESULTS</b>10 positive pooling were screened from 28800 samples; after further detection, 2 of these positive pooling were HBV-DNA negative and 8 HBV-DNA positive samples were found.The 10-week follow-up research on these 8 blood donors showed that 6 were HBV-DNA positive and HBsAg-negative at 2 weeks, 4 weeks, 6 weeks, 8 weeks, 10 weeks respectively, 1 was not HBsAg positive until 2 weeks and was positive on follow-up, and considered in "window period", 1 was HBV-DNA negative, HBsAg-negative on follow-up. Of these 8,7 were not only migrant laborers with poor condition of work, life and health but also in high risk of secondary infection for HBV, in addition they had little idea of therapy or prevention measures of HBV infection and the other 1 was HBV-DNA negative, HBsAg-negative on follow-up, who was in better condition than the above 7 donors.</p><p><b>CONCLUSION</b>NAT is more sensitive than ELISA in screening HBV, but the probability of being false positive of NAT can not be ignored at the same time. On the hand, only screening HBsAg for HBV is relative limitation in high infection region of China. Some factors would have effect on the serum conversion of blood donors including the quality of work and life, therapy or prevention measures.</p>


Subject(s)
Adult , Female , Humans , Male , Young Adult , Blood Donors , DNA, Viral , Blood , Genetics , Enzyme-Linked Immunosorbent Assay , Follow-Up Studies , Hepatitis B , Blood , Diagnosis , Hepatitis B e Antigens , Blood , Hepatitis B virus , Genetics , Allergy and Immunology , Mass Screening , Methods , Nucleic Acid Amplification Techniques , Methods , Reproducibility of Results , Sensitivity and Specificity
7.
Chinese Journal of Medical Genetics ; (6): 466-469, 2006.
Article in Chinese | WPRIM | ID: wpr-285097

ABSTRACT

<p><b>OBJECTIVE</b>To understand the genetic polymorphism of DC-SIGN's and DC-SIGNR's neck regions in normal Chinese Han population, and to obtain the genetic data of the two loci in Chinese Han population.</p><p><b>METHODS</b>The genotypes and alleles of repeat sequences of DC-SIGN and DC-SIGNR neck region were typed by PCR, agarose gel electrophoresis and sequencing. Polymorphism information content (PIC) of DC-SIGNR was calculated.</p><p><b>RESULTS</b>DC-SIGN genetic polymorphism was rare. Allele 7 was most and its frequency was 0.9808. 4-, 5-, 6- and 8- alleles were also found, although their frequencies were very low. Caucasians had only 6- and 8- allele mutants; DC-SIGNR genetic polymorphism was high, its PIC was 0.5312, 4-,5-,6-,7-,8-,9- alleles and 16 genotypes were found in normal Chinese Han population. The differences of 6/5,7/4,7/5,7/6,7/7,9/5,9/7,9/9 genotypes distribution and 5-,6-,7-,9- alleles frequency between normal Chinese Han population and Caucasian population were all extremely distinct (P<0.01). The inserted mutation seemed more in Chinese Hans than Caucasian population.</p><p><b>CONCLUSION</b>DC-SIGN and DC-SIGNR genotypes and alleles distribution in Chinese Han population are significantly different from Caucasian population and with Chinese own population genetic characteristics, compared with Caucasians.</p>


Subject(s)
Adolescent , Adult , Female , Humans , Male , Young Adult , Alleles , Asian People , Genetics , Cell Adhesion Molecules , Genetics , China , Gene Frequency , Genotype , Lectins, C-Type , Genetics , Polymerase Chain Reaction , Polymorphism, Genetic , Genetics , Receptors, Cell Surface , Genetics
8.
National Journal of Andrology ; (12): 296-298, 2005.
Article in Chinese | WPRIM | ID: wpr-323372

ABSTRACT

Chlamydia trachomatis may cause trachoma, pneumonia, urogenital infection, conjunctivitis and lymphogranuloma venereum, etc. This paper reviews the effects of monotherapy, combined antibiotic regimens, and drug resistance during the treatment of Chlamydia trachomatis infection.


Subject(s)
Female , Humans , Male , Pregnancy , Anti-Bacterial Agents , Pharmacology , Therapeutic Uses , Chlamydia Infections , Drug Therapy , Chlamydia trachomatis , Drug Resistance, Bacterial , Drug Therapy, Combination
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