1.Establishment and evaluation of an orthotopic transplantation tumor model derived from transgenic mouse with spontaneous pancreatic cancer
Qingling AN ; Dengxu TAN ; Ya ZHAO ; Caiqin ZHANG ; Changhong SHI
Acta Laboratorium Animalis Scientia Sinica 2024;32(1):1-8
		                        		
		                        			
		                        			Objective To establish an orthotopic transplantation tumor model of pancreatic cancer derived from transgenic LSL-KrasG12D/+ LSL-Trp53R172H/+ Pdx1-Cre(KPC)mice.To provide a stable and reliable drug preclinical research animal model to study the developmental mechanism and treatment strategies of pancreatic cancer.Methods Tumor tissue derived from KPC transgenic mice with spontaneous pancreatic cancer was transplanted into the C57BL/6J mouse pancreas.Ultrasound was used to monitor tumor growth.HE and immunofluorescence staining was used to evaluate the pathological characteristics of this model.Results The tumor derived from KPC mice grew steadily on the pancreas of C57BL/6J mice.Tumor cell proliferation index Ki67,matrix fibrosis marker αSMA,and immune cell markers CD45 and CD206 were all stably expressed in the tumor.The model stably retained the pathological features of primary pancreatic cancer.Widespread tumor metastases,which were similar to those observed in patients with pancreatic cancer,developed in this model.Conclusions An orthotopic transplantation model derived from a transgenic mouse with spontaneous pancreatic cancer was established successfully.The model simulates the stromal environment and immune cell infiltration of pancreatic cancer and retains strong stability and uniformity with the original tumor.It can be used as an effective drug preclinical research model to study pancreatic cancer progression and treatment strategies.
		                        		
		                        		
		                        		
		                        	
2.Predictive value of color Doppler ultrasound parameters for fetal growth restriction induced by gestational hypertension in high-altitude regions
Yongfeng ZHAO ; Guocai GAN ; Xue WANG ; Xu ZHAO ; Shumei MA ; Caiqin LI ; Cheng ZHANG
Journal of Clinical Medicine in Practice 2024;28(20):112-118
		                        		
		                        			
		                        			Objective To investigate the predictive value of color Doppler ultrasound parameters for fetal growth restriction (FGR) induced by hypertensive disorders of pregnancy in high-altitude regions. Methods Pregnant women with gestational hypertension who were treated between July 2020 and June 2022 at the Affiliated Hospital of Qinghai University (with altitude of 2, 300 meters, were divided into group A1 with 19 cases and group A2 with 51 cases according to occurrence of FGR), Yushu People's Hospital (with altitude of 3, 700 meters, were divided into group B1 with 25 cases and group B2 with 47 cases according to occurrence of FGR), and Civil Aviation Clinical Medical College of Peking University (plain region, control group with 71 cases) were enrolled in this study. All pregnant women in each group underwent fetal color Doppler ultrasound examination of the middle cerebral artery (MCA) and umbilical artery (UA) blood flow parameters, including pulsatility index (PI), resistance index (RI), systolic/diastolic ratio (S/D), peak systolicvelocity (PSV), and cerebroplacental ratio (CPR) at 28 weeks of gestation were detected. Multivariate Logistic regression analysis was performed to identify independent risk factors for FGR in pregnant women with gestational hypertension. Receiver operating characteristic (ROC) curves were plotted to analyze the predictive value of color Doppler parametersfor FGR. Results The UA blood flow parameters (PI, RI, S/D, PSV) of the fetuses in groups A1, A2, B1, and B2 were significantly higher than those in the control group, while the MCA blood flow parameters (PI, RI, S/D, PSV) and CPR were significantly lower (
		                        		
		                        	
3.Characterisation of the dynamics of MAOA/FOXA1 in the progression of neuroendocrine differentiation in prostate cancer
Hao HAN ; Hui LI ; Caiqin ZHANG ; Jumei ZHAO ; Xiaoli WEI ; Changhong SHI
Acta Laboratorium Animalis Scientia Sinica 2024;32(6):683-690
		                        		
		                        			
		                        			Objective To explore the dynamic changes in monoamine oxidase A(MAOA)and forkhead box A1(FOXA1)levels during neuroendocrine differentiation(NED)in prostate cancer,providing new strategies for the treatment of neuroendocrine prostate cancer.Methods Cell models and mouse transplantation models of NED were established through long-term sustained induction with enzalutamide(ENZ).Dynamic expression of MAOA and FOXA1 in NED was detected by Western Blot and Real-time PCR.GEO database data were selected to analyze the dynamic trends in MAOA and FOXA1 levels in multiple NED models.We constructed a mouse transplantation model of human prostate cancer cell lines and analyzed the dynamic expression of MAOA and FOXA1 in the in vivo NED model by immunohistochemistry.MAOA expression was disrupted with lentiviral transfection,and the impact on FOXA1 was detected.Results Both MAOA and FOXA1 concentrations showed dynamic characteristics,increasing and then decreasing during the NED process.Knockdown of MAOA in prostate cancer cells led to decreased expression of FOXA1.This MAOA may play different roles at different stages of NED by acting through FOXA1.Conclusions Both MAOA and FOXA1 levels showed increasing,then decreasing,trends during NED.The expression of MAOA affected the level of FOXA1,and MAOA/FOXA1 may play a dynamic regulatory role in the NED process.
		                        		
		                        		
		                        		
		                        	
4.Comparison of efficacy of single-port laparoscopic and multi-port laparoscopic lesion resection in patients with adenomyosis
Baoshuang GU ; Caiqin ZHAO ; Fangfang XU
Journal of Xinxiang Medical College 2024;41(11):1070-1074
		                        		
		                        			
		                        			Objective To investigate the efficacy of single-port laparoscopic versus multi-port laparoscopic lesion removal in patients with adenomyosis(AM).Methods Eighty patients with AM who were treated at Nanyang First People's Hospital from March 2020 to March 2023 were selected as the research subjects and divided into single-port group(n=40)and multi-port group(n=40).The patients in the single-port group underwent single-port laparoscopic lesion resection,and the patients in the multi-port group received multi-port laparoscopic lesion resection.The uterine volume,lesion area,pain degree,menstrual blood volume,levels of carbohydrate antigen 125(CA125),carbohydrate antigen 153(CA153)and sex hormone indexes[anti-Müllerian hormone(AMH)and estradiol(E2)],and clinical efficacy of treatment were compared in the two groups.Results There was no statistically significant difference in the uterine volume and lesion area of patients between the two groups before treatment(P>0.05).The uterine volume and lesion area of the patients in the two groups after treatment were lower than those before treatment(P<0.05);the uterine volume and lesion area of patients in the multi-port group were significantly lower than those in the single-port group after treatment(P<0.05).The visual analogue scale(VAS)scores and pictorial blood loss assessment chart(PBAC)scores of patients in the two groups before treatment had no significant difference(P>0.05).The VAS and PBAC scores of patients in the two groups after treatment were significantly lower than those before treatment(P<0.05);the VAS scores of patients in the multi-port group were significantly higher than those in the single-port group after treatment(P<0.05),and the PBAC scores in the multi-port group were significantly lower than those in the single-port group(P<0.05).There was no statistically significant difference in the serum CA125 and CA153 levels between the two groups before treatment(P>0.05).The serum CA125 and CA153 levels of patients in the two groups after treatment were significantly lower than those before treatment(P<0.05),and the CA125 and CA153 levels of patients in the multi-port group were significantly lower than those in the single-port group after treatment(P<0.05).There was no statistically significant difference in AMH and E2 levels between the two groups before treatment(P>0.05).After surgery,the AMH levels of patients in the two groups were significantly higher than those before surgery(P<0.05),and the E2 levels were significantly lower than those before surgery(P<0.05);the AMH levels of patients in the multi-port group were significantly higher than those in the single-port group(P<0.05),and the E2 levels were significantly lower than those in the single-port group(P<0.05).The overall effective rate of patients in the multi-port group and the single-port group was 85.00%(34/40)and 62.50%(25/40),respectively after surgery;the overall effective rate of patients in the multi-port group was significantly higher than that in the single-port group(x2=5.230,P<0.05).Conclusion Compared with single-port laparoscopic lesion excision,multi-port laparoscopic lesion excision for AM can effectively reduce uterine volume and lesion area and improve menstrual blood volume,CA125 and CA153 levels,and sex hormone level with superior efficacy;however,due to the number of surgical incisions,the degree of pain of patients after the operation is more serious.
		                        		
		                        		
		                        		
		                        	
5.Construction and Evaluation of Theranostic Near-infrared Fluorescent Probe for Targeting Inflammatory Brain Edema
Jing QIN ; Yong ZHAO ; Caiqin ZHANG ; Bing BAI ; Changhong SHI
Laboratory Animal and Comparative Medicine 2024;44(3):243-250
		                        		
		                        			
		                        			Objective A novel compound based on near-infrared fluorescence(NIRF)probe was prepared to achieve dynamic monitoring of an inflammatory brain edema model in mice and real-time evaluation of therapeutic effects through in vivo imaging.Methods The NIRF probe IR-783 was chemically linked with clinical brain edema therapeutic drug furosemide(FSM)to obtain the new compound,IR-783-FSM.The ultraviolet fluorescence properties of the compound were evaluated using an ultraviolet spectrophotometer.The uptake of the compound by mouse macrophage cells RAW 264.7 was detected with in vitro cellular experiments.Its cytotoxicity was evaluated through CCK8 assays.A brain edema model was established in BALB/c mice via intraperitoneal injection of lipopolysaccharide(LPS),confirmed by HE staining and dry-wet weight methods for brain tissues.The mice in the brain edema model were divided into control group,IR-783,and IR-783-FSM treatment groups,receiving intraperitoneal injections of PBS,IR-783,and IR-783-FSM,respectively.Real-time in vivo fluorescence imaging was then performed.The mice in each group were euthanized after 10 hours.Ex vivo brain imaging and dry-wet weight measurements were performed to observe the NIRF imaging characteristics and therapeutic effects of IR-783-FSM on brain edema model.Results The newly synthesized compound,IR-783-FSM,retained the excellent near-infrared fluorescence characteristics of IR-783.It could target mouse macrophages with an IC50 of 48.82 μmol/L.A brain edema model could be successfully constructed with intraperitoneal injection of LPS,with significantly higher brain tissue water content compared to the control group(P<0.01).In vivo imaging showed that IR-783-FSM had a significantly stronger fluorescence signal in the brain edema model than IR-783.Compared to the control group,the brain water content was significantly reduced in the 2,5,and 8 mmol/L IR-783-FSM treatment groups(P<0.01).Conclusion The newly synthesized NIRF probe IR-783-FSM facilitates dynamic monitoring of brain edema and real-time evaluation of therapeutic effects.
		                        		
		                        		
		                        		
		                        	
6.Diagnostic value of ultrasound diagnosis of fetal intrauterine distress in high-risk puerperae in plateau areas
Yongfeng ZHAO ; Guocai GAN ; Xue WANG ; Xu ZHAO ; Shumei MA ; Caiqin LI ; Cheng ZHANG
Tianjin Medical Journal 2023;51(12):1374-1378
		                        		
		                        			
		                        			Objective To explore the diagnostic value of color Doppler ultrasound for fetal intrauterine distress(FIUD)in high-risk puerperae in plateau areas.Methods A total of 130 puerperae in plateau areas and 130 puerperae in plain areas were enrolled.According to presence or absence of FIUD in different areas,they were divided into the plateau distress group(47 cases),the plateau normal group(83 cases),the plain distress group(31 cases)and the plain normal group(99 cases).All cases underwent blood flow detection of middle cerebral artery(MCA)and umbilical artery(UA)before delivery,and cerebral-placental ratio(CPR)was calculated.The incidence of FIUD was compared between high-risk puerperae in plateau area and in plain area.Gestational age,birth weight,cesarean section rate and blood spectrum parameters of MCA and UA were compared between the four groups.The predictive value of color Doppler ultrasound parameters for FIUD was analyzed by receiver operating characteristic(ROC)curves.Results The incidence rates of FIUD and severe FIUD were higher in patients of plateau areas than those in plain areas(36.15%,13.85%vs.23.85%,4.62%,P<0.05).Compared with the plateau distress group,gestational age and birth weight were increased in the plateau normal group and the plain distress group(P<0.05).Compared with the plateau distress group,PI,RI,S/D and CPR of MCA were increased,while PI,RI and S/D of UA were decreased in the plateau normal group and the plain distress group(P<0.05).Results of ROC curve analysis showed that overall performance advantage of S/D of UA was the most obvious in the diagnosis of FIUD in high-risk puerperae in plateau areas.The diagnostic sensitivity of RI of MCA was the highest,and the diagnostic specificity of CPR was the highest(P<0.05).Conclusion Color Doppler ultrasound has good diagnostic value for FIUD in high-risk puerperae in plateau areas,which can be applied as an effective clinical screening means for FIUD.
		                        		
		                        		
		                        		
		                        	
7.Exploration of Laboratory Animal Science Teaching Practice from Perspectives of Curriculum Ideology and Politics
Ya ZHAO ; Caiqin ZHANG ; Han MENG ; Jing QIN ; Bing BAI ; Yong ZHAO ; Xu GE ; Changhong SHI
Laboratory Animal and Comparative Medicine 2023;43(6):641-646
		                        		
		                        			
		                        			The ideological and political content of the laboratory animal science degree course with the basic task of "cultivating morality and cultivating people" is organically integrated into the teaching system of laboratory animal science. It can have a subtle influence on students' thoughts and behaviors. Combined with the curriculum design and professional characteristics of laboratory animal science, this article discussed the ideological and political elements contained in this course, proposed the forms and methods of integrating ideological and political elements into the curriculum design in each chapter. Additionally, the typical cases and characteristic practices of the organic connection of ideological and political education in the teaching system of laboratory animal science were summarized. Practice has proved that integrating the ideological and political elements into the teaching system of laboratory animal science can enhance teacher's awareness and ability of politics, thus effectively improving the compre-hensive quality of students and enhancing the effectiveness of ideological and political education in laboratory animal science. 
		                        		
		                        		
		                        		
		                        	
8.Establishing a Genetic Detection Protocol of Single Nucleotide Polymorphisms Panels in Inbred Rats Based on Multiplex PCR-LDR
Liya ZHAO ; Liju NI ; Caiqin ZHANG ; Jianping TANG ; Yangzheng YAO ; Yanyan NIE ; Xiaoxue GU ; Ying ZHAO
Laboratory Animal and Comparative Medicine 2023;43(5):548-558
		                        		
		                        			
		                        			ObjectiveTo establish a set of single nucleotide polymorphisms (SNP) detection protocol for inbred rats based on multiplex PCR-ligase detection reaction (LDR). MethodsA total of 40 rats SNP sites were selected on chromosomes 1-20 and X of rats among 5 inbred strains of rats, and the 40 SNP sites were randomly divided into four groups. A genetic detection protocol for 4 groups of SNP in inbred rats based on multiplex PCR-LDR technology was constructed. 9 commonly used rat strains from two other domestic rat suppliers were detected by this protocol. Finally, the feasibility of this protocol was verified by comparing the amplification effects of different DNA polymerases by a third-party laboratory. ResultsWhen using the constructed SNP detection protocol for inbred rats to test 5 rat strains, all sites in each sample obtained good amplification results. The 9 commonly used rat strains from two other rat suppliers in china were also well amplified by this SNP detection protocol, and 40 SNPs were homozygous in each Inbred strain. The results of detection of the same rat DNA samples with three different DNA polymerases showed that the Multiplex PCR Kit, AmpliTaq Gold 360 DNA polymerase and Platinum II Taq hot start DNA polymerase had electrophoretic peaks of amplification products at all SNP sites in groups 1 to 3, and Platinum II Taq hot start DNA polymerase had one less electrophoretic peak of the amplification products at the SNP sites in group 4. In addition, inter-laboratory comparisons showed consistent results for the same amplification system. ConclusionBased on multiplex PCR-LDR technology, this study successfully established a SNP detection protocol for rats covering all autosomes and X chromosomes with the excellent stability and repeatability. 
		                        		
		                        		
		                        		
		                        	
9.Prenatal diagnosis and postnatal follow-up of 27 cases with 15q11.2 BP1-BP2 microdeletion syndrome
Yu CUI ; Jianping XIAO ; Lan YANG ; Minya SUN ; Li ZHAO ; Caiqin GUO ; Xin ZHAO ; Heng ZHANG
Chinese Journal of Perinatal Medicine 2022;25(4):271-277
		                        		
		                        			
		                        			Objective:To summarize the prenatal diagnosis and postnatal follow-up of 15q11.2 BP1-BP2 microdeletion syndrome (Burnside-Butler syndrome, BBS), and provide a reference for the management of BBS.Methods:A retrospective analysis was performed on 27 singleton pregnancies with fetal BBS that were prenatally diagnosed by single nucleotide polymorphism(SNP) array of amniotic fluid in Wuxi Maternity and Child Health Care Hospital from January 2017 to September 2021. Prenatal diagnosis indications, serological screening, prenatal ultrasound features, SNP array results, and postnatal growth and development were described and summarized.Results:(1) Of the 27 cases, the indications of prenatal diagnosis in 14 cases were abnormal sonographic findings, including eight cases with increased nuchal translucency, two with cleft lip and palate/alveolar process cleft, one with fetal multiple joint contracture syndrome, one with fetal right diaphragmatic hernia and single umbilical artery, one with suspected fetal duodenal atresia and one with nasal bone absence. Other indications included high risk of Down syndrome by serological screening in six cases, history of adverse pregnancy in six cases, and advanced age in one case. (2) Karyotyping of amniotic fluid in these 27 BBS fetuses showed normal results and SNP array indicated the deletion range of 311.8-855.3 kb. Parental verification of 23 cases confirmed one was a new mutation, seven were inherited from the father and 15 from the mother. (3) Five pregnancies were terminated in the second trimester and the remaining 22 cases were live births. (4) The median follow-up of the 22 children was 1 year 8 months (range 0.5 months to 4 years 3 months), which found low body weight and/or growth retardation in six cases, low body weight with language retardation in one case, low body weight with growth retardation and hyperactive behavior in one case, language retardation with left ear appendage in one case, cleft palate accompanied by duodenum/cleft lip and alveolar cleft in two cases without abnormal development after surgical treatment, and no abnormal growth in the remaining 11 cases.Conclusion:For BBS fetuses, the proportion of ultrasound abnormalities is high but with a low specificity in prenatal diagnosis, and the risk of abnormal postnatal growth and development/behavior is high, which requires continuous monitoring.
		                        		
		                        		
		                        		
		                        	
10.Prenatal diagnosis of Jacobsen syndrome in a fetus carried by a pregnant woman with intellectual disability.
Caiqin GUO ; Junfeng WANG ; Ye TANG ; Hao SHI ; Jun LIU ; Li ZHAO
Chinese Journal of Medical Genetics 2019;36(8):826-288
		                        		
		                        			OBJECTIVE:
		                        			To assess the value of combined cytogenetic and molecular techniques for the prenatal diagnosis of a pregnant woman with intellectual disability (ID).
		                        		
		                        			METHODS:
		                        			The fetus and its parents were subjected to G-banding karyotyping analysis, single nucleotide polymorphism array (SNP-array) and fluorescence in situ hybridization (FISH) analysis.
		                        		
		                        			RESULTS:
		                        			G-banding karyotype analysis revealed that the woman has carried a chromosomal microdeletion 46,XX,del(11)(q24), and the fetus was a carrier of 46,XN,del(11)(q24)mat. Subsequent SNP-array and FISH analysis of the pregnant woman indicated that the microdeletion has mapped to 11q24.1-q25. Both the pregnant woman and her fetus were diagnosed with Jacobsen syndrome.
		                        		
		                        			CONCLUSION
		                        			Combined use of cytogenetic and molecular genetic techniques can facilitate diagnosis of patients with intellectual disability.
		                        		
		                        		
		                        		
		                        			Chromosome Deletion
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		                        			Female
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		                        			Fetus
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		                        			Humans
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		                        			In Situ Hybridization, Fluorescence
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		                        			Intellectual Disability
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		                        			Jacobsen Distal 11q Deletion Syndrome
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		                        			diagnosis
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		                        			Karyotyping
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		                        			Polymorphism, Single Nucleotide
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		                        			Pregnancy
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		                        			Prenatal Diagnosis
		                        			
		                        		
		                        	
            

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