1.The discussion of teaching quality monitoring operating mechanism in medical college under the new situation
Bing JIA ; Fengyan JIANG ; Yunfei CAO
Chinese Journal of Medical Education Research 2003;0(04):-
With clinical medical professional certification as a background and combining Guangxi Medical University Teaching Quality Monitoring System of practical experiences,the author pointed out that internal teaching quality monitoring system problems during the operation,discussed the constraints of issues affecting the effective functioning of the teaching quality monitoring,and proposed corresponding suggestions.
2.Adiponectin reduces apoptosis by improving myocardial anti-oxidative activity after myocardial ischemia/reperfusion injury in diabetic rats
Jia GUO ; Yunfei BIAN ; Chuanshi XIAO ; Zhidong LI
Chinese Pharmacological Bulletin 2014;(5):623-627
Aim To study the effect of adiponectin ( APN) on myocardial ischemia reperfusion( IR) injury in diabetic rats and to explore the role of oxidation-an-tioxidation system. Methods Male Sprague Dawley rats were randomly divided into control group( NS) , IR group ( NIR ) , diabetes group ( DS ) , DS + IR group (DIR), DS +APN +IR group(APN). Experimental diabetes was induced in the animals by a single intrap-eritoneal injection of streptozotocin at a dose of 55 mg ·kg-1 . The IR and NIR group were subjected to myo-cardial I/R injury. APN group was administered APN through intravenous injection 10 min before the reper-fusion, the others were administered normal saline. The rats were considered diabetic and used for the study only if their glucose levels were higher than 15 mmol·L-1. Results All the diabetic rats exhibited increased levels of blood glucose and reduction of body weight ( P <0. 05 ) . Compared with those of NS and DS groups, the myocardial infarct size, cardiomyocyte apoptosis, MDA concentration and ROS in NIR and DIR groups were remarkably increased, activities of SOD and NO were decreased(P<0. 05 or P<0. 01). APN decreased oxidative stress product generation and myocardial apoptosis induced by diabetic myocardial I/R injury ( P <0. 05 ) . Conclusion APN exerts pro-tective effect on myocardial I/R injury in diabetic rats through anti-oxidative mechanism.
3.Clinical study on treatment of patients with upper digestive tract malignant tumors of middle and late stage with Ginkgo biloba exocarp polysaccharides capsule preparation
Huasheng CHEN ; Fan ZHAI ; Yunfei CHU ; Fang XU ; Aihua XU ; Linchang JIA
Journal of Integrative Medicine 2003;1(3):189-91
OBJECTIVE: To observe the clinical efficacy of Ginkgo biloba exocarp polysaccharides (GBEP) capsule preparation in treating upper digestive tract malignant tumors of middle and late stage. METHODS: Eighty-six patients of the upper digestive tract malignant tumors were treated with GBEP capsule preparation taken orally. The clinical symptoms and the qualities of life of the patients with single GBEP and combined with operation, radiotherapy or intervention chemotherapy were observed. The tumor size was measured by electronic gastroscope before and after treatment with single GBEP. Objective response rate (RR) of the tumor was calculated. The survival period of patient was observed. The changes of blood routine examination in the patients treated with radiotherapy were observed. RESULTS: GBEP preparation could markedly improve the patients'clinical symptoms. Karnofsky scoring of the patients markedly increased after treatment. There were 2 CR (complete response, 6.3%), 22 PR (partial response, 68.8%)and 5 SD (stable disease, 15.6%) of 32 cases with single GBEP preparation. The survival periods of the 32 cases were markedly prolonged. The preparation could relieve the inhibited hematopietic function and the weight loss due to radiotherapy. CONCLUSION: GBEP capsule preparation has some definite therapeutic effects on upper digestive tract malignant tumors of middle and late stage.
4.Gene cloning, expression and activity detection of porcine interleukin-18 mature protein in Escherichia coli.
Lanlan ZHENG ; Yunfei JIA ; Baoan CUI ; Hongying CHEN ; Zhanyong WEI ; Ruiliang CHEN
Chinese Journal of Biotechnology 2008;24(2):214-219
Porcine interleukin-18 mature protein gene was amplified from porcine spleen cells by RT-PCR. PCR product was cloned into the T vector pGEM-T for sequencing. The nucleotide sequence of this gene was 474 bp. Then, it was subcloned into the prokaryotic expressing plasmid vector pGEX6P-1 and transformed into host E. coli strain BL21 for expression. The expression of pIL-18 mature protein gene was identified by SDS-PAGE .The expression product was fusion protein with molecular weight of 45 kD and the percentage of expression protein in E. coil protein was 28%. The protein was purified by washing of inclusion bodies and the activity was measured by methyl thiazolyl tetrazolium (MTT).
Amino Acid Sequence
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Animals
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Base Sequence
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Cloning, Molecular
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Escherichia coli
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genetics
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metabolism
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Interleukin-18
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biosynthesis
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genetics
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Molecular Sequence Data
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Recombinant Fusion Proteins
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biosynthesis
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genetics
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immunology
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Swine
5.Reproductive system recurrence after hematopoietic stem cell transplantation for acute myeloid leukemia: a report two cases
Yunfei GAO ; Xin ZHAO ; Yehui TAN ; Fei SONG ; Jia LI ; Sujun GAO ; Xiaoliang LIU
Chinese Journal of Organ Transplantation 2024;45(2):115-118
For two young female patients with extramedullary recurrence of reproductive system after allogeneic hematopoietic stem cell transplantation for acute myeloid leukemia. And the characteristics of extramedullary relapse of reproductive system are summarized for exploring possible effective treatments.
6.Challenges and suggestions for human genetic resource management in international cooperation of medical institutions caused by the Implementation Rules of the Regulations on the Management of Human Genetic Resources: A case study of Peking University Cancer Hospital
Shuanglei KONG ; Yunfei GENG ; Luopei WEI ; Lingling BAI ; Shuqin JIA
Chinese Journal of Medical Science Research Management 2024;37(1):18-21
Objective:According to the international cooperation project of Peking University Cancer Hospital on human genetic resource management practices, combined with the development direction of human genetic resource management laws and regulations, and propose reference suggestions for medical institutions to strengthen human genetic resource management.Methods:Sort out the projects that Peking University Cancer Hospital obtained international cooperation approval on the government platform of the Ministry of Science and Technology from July 2019 to June 2023, analyze the current situation of human genetic resource management in the hospital, summarize the challenges brought by the implementation of new regulations on human genetic resource management in medical institutions, and propose corresponding suggestions.Results:A total of 1276 international cooperation projects on human genetic resources have been approved, including 345 initial declarations and 931 change declarations. Involving 453 studies, including 286 clinical trials of drugs or devices on the market, accounting for 63.13%, and 100 clinical trials of Phase I drugs, accounting for 34.97% of the market studies. On average, there are 3.14 changes per project for listed research, and 1.56 changes per project for non listed research.Conclusions:Regulations on the Management of Human Genetic Resources ( short for Rules) limit the management scope of international cooperation projects involving human genetic resources and delegate management authority to medical institutions. Adjusting the scope of application for international cooperative clinical trial filing may result in some administrative approval projects being transferred to filing. The approval process for international cooperative scientific research projects on human genetic resources has been adjusted. Suggest medical institutions to strengthen the management of samples and intellectual property outside the scope of application of Rules.Strengthen the entire process management of international cooperation in scientific research. Pay attention to and timely communicate the dynamics of human genetic resource management.
7.Discussion on acceptance limit of drug metabolites in quality standard
Yunfei LIU ; Lingbo WANG ; Xiulan WU ; Jia YU ; Hao ZHOU ; Lihong YANG
Drug Standards of China 2024;25(5):526-528
This paper discussed how to set the limit of impurities in the quality standard when the impurities in small-molecular innovative drugs were metabolites.Firstly,through the analysis and interpretation of each relevant guideline,in combination with the review cases of FDA and EMA,found out the conditions for qualification of im-purity,and then establ ish the acceptable limit of impurities based on the test results of multiple batches,the incre-ments of production process and storage process.
8.Effects of long non-coding RNA C10orf25 targeting miRNA-671-5p on the proliferation and invasion of prostate cancer cells
Yunfei ZHAO ; Xiaoying WANG ; Fang XIE ; Geng HUANG ; Hong WANG ; Jia LIU
Cancer Research and Clinic 2024;36(7):509-514
Objective:To explore the effect of long non-coding RNA (lncRNA) C10orf25 on the proliferation and invasion ability of prostate cancer cells and the possible role of miRNA-671-5p (miR-671-5p).Methods:Data from the Gene expression omnibus (GEO) database (data updated in January 2023) were used to analyze the differences in the expression levels of C10orf25 in 137 cases of prostate cancer tissues and paracancerous tissues. Prostate cancer C4-2B, DU-145, 22Rv1, PC-3, LNCaP cell lines and immortalized prostate epithelial RWPE-1 cell lines were selected, and then real-time quantitative fluorescence polymerase chain reaction (qRT-PCR) was used to detect the relative expression levels of C10orf25 in cell lines. The 22Rv1 cells with the lowest relative expression level of C10orf25 were selected and divided into the control group (transfected with negative plasmid) and the C10orf25 group (transfected with C10orf25 plasmid); the CCK-8 method was used to detect the proliferation activity of 22Rv1 cells in both groups at day 1, 2, 3, 4, 5 (expressed as absorbance value); the Transwell method was used to detect the invasion ability of 22Rv1 cells. Linc2GO software was used to predict miR-671-5p with binding sites for C10orf25. Dual luciferase reporter gene assay was used to verify the targeting relationship between C10orf25 and miR-671-5p. qRT-PCR was used to detect the relative expression levels of C10orf25 and miR-671-5p. Western blot was used to detect the expression of proteins related to the NF-κB signaling pathway of 22Rv1 cells in the both groups.Results:In the GEO database, the relative expression level of C10orf25 in prostate cancer tissues was lower than that in paracancerous tissues ( P < 0.01). The relative expression levels of C10orf25 in immortalized prostate epithelial cell line RWPE-1 and prostate cancer cell lines C4-2B, DU-145, 22Rv1, PC-3, and LNCaP were 1.00±0.05, 0.63±0.04, 0.42±0.03, 0.18±0.04, 0.81±0.02, 0.50±0.07, and the difference was statistically significant ( F = 43.29, P < 0.05). The proliferation ability of 22Rv1 cells in C10orf25 group was lower than that in the control group from the second day, and the differences were statistically significant (all P < 0.05). The number of invasive cells in the control group and C10orf25 group were (97±11) and (36±9), respectively, and the difference was statistically significant ( t = 4.15, P < 0.01). Linc2GO software prediction results showed that C10orf25 had a binding site for miR-671-5p. The dual luciferase reporter gene assay showed that the relative luciferase activity of miR-671-5p and C10orf25 wild plasmid co-transfecting 22Rv1 cells was lower than that of miR-NC and C10orf25 wild plasmid co-transfecting 22Rv1 cells, and the difference was statistically significant ( P < 0.01); when miR-671-5p or miR-NC was co-transfected with C10orf25 mutant plasmid, the difference in the luciferase activity of 22Rv1 cells was not statistically significant ( P > 0.05). The relative expression levels of miR-671-5p in 22Rv1 cells were 7.33±0.99 and 0.98±0.16, respectively in the control group and C10orf25 group, and the difference was statistically significant ( t = 6.32, P < 0.01). The results of Western blot showed that the expression levels of NF-κB signaling pathway protein p50, matrix metalloproteinase 9, c-myc, and vascular endothelial growth factor protein in 22Rv1 cells in C10orf25 group were lower than those in the control group. Conclusions:The overexpression of C10orf25 may inhibit the proliferation and invasion of prostate cancer cells through the miR-671-5p-NF-κB axis.
9.Stasis-removing phlegm-resolving formula reduces hepatic lipid deposition in rabbits with atherosclerosis through regulating mitochondrial autophagy related proteins
Si CHEN ; Lianqun JIA ; Nan SONG ; Jian WANG ; Ning CHEN ; Yunfei GAO ; Simeng XIE
Journal of Beijing University of Traditional Chinese Medicine 2018;41(4):310-315
Objective To observe the effect of stasis-removing phlegm-resolving formula (Huayu Qutan Fang, HYQTF) on liver mitochondrial autophagy related proteins, and to investigate the effects of mitochondrial autophagy on liver lipid deposition in rats with atherosclerosis (AS). Methods Rabbits (60-SPF-grade Zelanian purebred males) were randomly divided into normal group,model group,HYQTF group and simvastatin group. Normal group was fed with normal diet; model group, HYQTF group and simvastatin group were fed with high-fat diet. 8 weeks after the modeling, HYQTF group and simvastatin group received corresponding medicinal intervention while normal group and model group were administered with the same volume of saline. After 4 weeks,the serum contents of total cholesterol (TC),triglyceride (TG), low-density lipoprotein-cholesterol (LDL-C) and high-density lipoprotein-cholesterol (HDL-C) were measured whereas the morphological changes of rabbit liver tissue were observed by using stained HE. Accumulation of lipid droplets was evaluated with oil red O staining, and the relative expression of autophagy relating protein FUNDC1,P62 and LC3 in rabbit liver tissue were detected with Western blotting method. Results Compared with normal group,TC,TG and LDL-C levels of serum increased significantly (P<0.01) whereas HDL-C level decreased (P<0.05) in the model group. Compared with the model group,serum TC,TG and LDL-C levels in the HYQTF group and simvastatin group decreased significantly (P<0.05),and the content of HDL-C increased significantly(P<0.05). HE staining results:The liver tissue of model group rabbits became apparently swollen and formed fatty vacuolization. Fatty vacuoles in HYQTF group and simvastatin group significantly decreased or disappeared. Normal morphology of liver tissue fully or partially recovered. Oil Red O staining results: In the model group, liver cell became swollen and round,with the loose cytoplasm and obvious accumulation of intracellular lipid droplets. The degree of steatosis decreased in HYQTF group and simvastatin group, with the number of lipid vacuoles decreased. Western blotting results:Compared with normal group,the relative expression of mitochondrial autophagy relating proteins LC3 and FUNDC1 in liver tissue of rabbits significantly increased in the model group (P <0.05), and the relative expression level of P62 decreased significantly (P <0.05) in the model. Compared with the normal group, mitochondrial autophagy relating protein LC3, FUNDC1 expression in model group increased significantly (P <0.05), while mitochondrial autophagy relating protein LC3,FUNDC1 expression in HYQTF group and simvastatin group decreased significantly,and the relative expression level of P62 increased significantly (P<0.05). Conclusion Stasis-removing phlegm-resolving formula may reduce lipid deposition in liver tissue of AS rabbits by regulating mitochondrial autophagy related proteins,thereby slowing the formation and development of atherosclerosis.
10.Mining and analysis of adverse drug reaction signals of melphalan based on FAERS
Panpan DI ; Hai LIANG ; Jie WANG ; Yunfei HU ; Shuyun JIA
China Pharmacy 2023;34(12):1493-1497
OBJECTIVE To mine the adverse drug reaction (ADR) signals of melphalan, so as to provide reference for clinically safe drug use. METHODS Using OpenVigil 2.1 data platform, relative ADR reports of melphalan from the first quarter of 2004 to the second quarter of 2022 in FAERS database were collected; data mining was conducted using the reported odds ratio (ROR) method and Medicines and Healthcare Products Regulatory Agency (MHRA) method of disproportional method. ADR reports were described and classified according to the system organ class (SOC) and preferred term (PT) in Medical Dictionary for Regulatory Activities (24.0 edition). RESULTS A total of 17 046 ADR reports related to the target drug melphalan were retrieved, and the number of ADR reports showed a fluctuating upward trend; the majority of patients were male (43.28%), and were concentrated between the ages of 50-<75 (35.09%), with the main reporting country being the United States (23.97%); ADR report involved a total of 22 842 severe outcomes, mainly including hospitalization or extended hospitalization (24.45%). Totally 403 ADR signals were detected, involving 23 SOC, mainly including blood and lymphatic system diseases (801 cases, 13.77%), followed by eye organ diseases (755 cases, 12.97%) and infectious and invasive diseases (716 cases, 12.30%). The ADR signals ranked high in the number of reported cases included febrile neutropenia, diarrhea, fever and mucositis and other PT; PT such as pneumonia, sepsis, vitreous hemorrhage, chorioretinal atrophy, myelodysplastic syndrome were not recorded in drug instructions. The ADR signals with high signal strength ranking included choroidal dystrophy, chorioretinal atrophy, eyeball atrophy and other PT, and above three types of PT were not included in the drug instructions. CONCLUSIONS ADRs caused by melphalan mainly include blood and lymphatic system diseases, eye organ diseases, and infectious and invasive diseases; before using melphalan, it is necessary to evaluate the drug use of patients, and pay close attention to the patient’s blood indicators and eye toxicity reaction, so as to guarantee the safety of treatment.