MMP9、FeNO以及血清IgE与儿童哮喘急性发作严重程度的相关性分析

目的研究呼出气一氧化氮(FeNO)、血清免疫球蛋白E(IgE)和基质金属蛋白酶9(MMP9)的水平与儿童哮喘急性发作之间的关系,为儿童哮喘的预防及治疗提供依据。方法选取沈阳市妇婴医院于2020年11月至2022年11月收治的98例支气管哮喘急性发作期儿童作为急性组,按照病情程度分成轻度组(n=32)、中度组(n=38)和重度组(n=28),按照2∶1的比例选出49例同期在门诊治疗的处于支气管哮喘缓解期的儿童作为缓解组,随机选取健康体检儿童49例作为健康对照组,分别对他们进行FeNO、MMP9和血清IgE及肺功能[用力肺活量(FVC)、1秒用力呼气量(FEV_(1))、FEV_(1)/FVC%、最大呼气流量(PEF)]检测。应用Pearson相关分析探讨哮喘急性发作期FeNO、MMP9及血清IgE和肺功能之间的联系,并对三者在支气管哮喘急性发作中的预测价值进行分析。结果急性组、缓解组和对照组的年龄、性别、体重指数和病程的比较,差异无统计学意义(P>0.05)。急性组FeNO、MMP9、血清IgE分别为(59.95±12.65)ppb、(4.87±1.44)pg/ml、(330.63±74.88)IU/ml,缓解组分别为(25.23±8.23)ppb、(1.21±0.02)pg/ml、(152.23±32.12)IU/ml,均高于对照组的(12.43±4.09)ppb、(0.53±0.24)pg/ml、(126.34±57.33)IU/ml,差异具有统计学意义(P<0.05)。急性期和缓解期FVC、FEV1、FEV1/FVC%、PEF均低于对照组,差异具有统计学意义(P<0.05)。支气管哮喘急性发作中度组FeNO、MMP9、血清IgE水平分别为(49.23±6.23)ppb、(1.21±0.02)pg/ml、(282.61±59.83)IU/ml,重度组分别为(67.43±10.09)ppb、(0.53±0.24)pg/ml、(356.49±70.82)IU/ml,均高于轻度组的(34.62±10.65)ppb、(4.87±1.44)pg/ml,(189.21±14.33)IU/ml,差异具有统计学意义(P<0.05)。在轻度组中FeNO、MMP9和血清IgE水平均较低,而在中度组中这些指标均较高,其中FVC、FEV_(1)、FEV_(1)/FVC%和PEF均较低,差异具有统计学意义(P<0.05)。FeNO以及MMP9与血清IgE水平呈正相关(P<0.05),FeNO、MMP9以及血清IgE水平与FVC、FEV_(1)、FEV_(1)/FVC%、PEF均呈负相关(P<0.05)。MMP9在支气管哮喘的诊断中表现出了显著的优势,当达到最大约登指数时,对应的截断值为1.17,曲线下面积(Area under curve,AUC)为0.83,敏感度和特异性也分别达到了90.13%和86.5%。结论支气管哮喘急性发作的儿童血清中的FeNO、MMP9以及血清IgE水平显著增高,随肺部功能恶化程度加重而上升,可能与支气管哮喘急性发作患儿肺功能损害程度有关。

Knock-out of GhPDCT with the CRISPR/Cas9 system increases the oleic acid content in cottonseed oil

Cotton is a pivotal economic crop for natural textile fibers that also serves as an important source of edible oil(Long et al.2023).Cottonseed oil contains approximately14%oleic acid and 59%linoleic acid.An increase in monounsaturated fatty acids,particularly oleic acid,enhances the oxidative stability and nutritional value of edible oil(Chen et al.2021).

微种植体支抗用于骨性错牙合畸形患者的疗效及对血清MMP-8、MMP-9、NO、IGF-1水平的影响

目的观察微种植体支抗用于骨性错牙合畸形患者的疗效及对血清基质金属蛋白酶8(MMP-8)、基质金属蛋白酶9(MMP-9)、一氧化氮(NO)、胰岛素样生长因子-1(IGF-1)水平的影响。方法前瞻性选取2022年2月至2023年12月在沧州市中心医院进行诊治的骨性错牙合畸形患者84例作为研究对象,按照随机数字表法将其分为观察组(n=42)和对照组(n=42)。观察组采用微种植体支抗治疗,对照组采用口外弓支抗治疗,统计两组治疗前和治疗6个月后的口腔结构、上下颌骨角度[上齿槽座角(SNA)、下齿槽座角(SNB)、上齿槽座点及鼻根点与下齿槽座点形成角(ANB)]、血清MMP-8、MMP-9、NO、IGF-1水平,记录两组美学满意度及并发症发生情况。结果在口腔结构方面,观察组磨牙移位为(3.21±0.84)mm,显著低于对照组[(5.32±1.11)mm],上中切牙凸距差、中切牙倾角差分别为(4.24±1.66)mm、(26.42±4.38)°,均显著高于对照组[(2.45±1.21)mm、(12.44±3.05)°],差异均有统计学意义(P<0.05)。治疗6个月后,观察组SNA、ANB分别为(72.01±2.19)°、(4.68±0.78)°,显著低于对照组[(76.49±2.21)°、(5.37±0.82)°],SNB为(78.65±2.36)°,显著高于对照组[(76.07±2.44)°],差异均有统计学意义(P<0.05)。治疗6个月后,观察组血清MMP-8、MMP-9、NO、IGF-1水平分别为(94.16±10.84)μmol/L、(74.49±9.87)pg/mL、(55.72±8.03)μmol/L、(643.85±26.32)ng/mL,显著低于对照组[(112.51±11.02)μmol/L、(86.52±10.01)pg/mL、(67.96±8.41)μmol/L、(703.36±26.96)ng/mL],差异均有统计学意义(P<0.05)。在美学满意度方面,观察组总满意度为92.86%,明显高于对照组(76.19%),差异有统计学意义(P<0.05)。在并发症方面,观察组总发生率为9.52%,明显低于对照组(30.95%),差异有统计学意义(P<0.05)。结论微种植体支抗治疗骨性错牙合畸形疗效较好,可以有效改善患者口腔结构和上下颌骨角度,调节血清MMP-8、MMP-9、NO、IGF-1水平,且美学满意度高,并发症少,值得临床推广应用。

基于CRISPR/Cas9技术建立Lepr与eNos双基因敲除的糖尿病肾病小鼠模型

目的基于CRISPR/Cas9基因编辑技术建立瘦素受体基因(leptin receptor,Lepr)与血管内皮一氧化氮合酶基因(endothelial nitric oxide synthase,eNos)双基因敲除(double-knockout,DKO)小鼠模型,构建晚期糖尿病肾病小鼠模型。方法根据eNos基因制备对应的gRNA,将CRISPR-Cas9体系显微注射于C57BL/Ks(BKS)背景小鼠的受精卵内。将受精卵转移至有假孕状态雌性小鼠的输卵管内部。幼鼠出生后经聚合酶链反应(polymerase chain reaction,PCR)鉴定及测序分析分选出为eNos^(+/-)基因型的F0代阳性小鼠,获得BKS背景下的Lepr基因杂合小鼠,即基因型为Lepr^(db/m)的Lepr-F0代杂合子小鼠。将eNos-F0与Lepr-F0代小鼠杂交,获得eNos^(+/-)/Lepr^(db/m)双杂合F1代小鼠,将双杂合F1代小鼠进一步交配,筛选得到Lepr与eNos双基因敲除小鼠。采用PCR法鉴定小鼠基因型,按基因鉴定结果分为野生型(wild-type,WT)组与DKO组小鼠。监测各组小鼠体质量、血糖与饮水进食量;采用酶联免疫吸附法(enzyme-linked immunosorbent assay,ELISA)检测小鼠尿白蛋白与尿肌酐水平,并计算尿白蛋白排泄率;苏木精-伊红(hematoxylin-eosin,HE)与过碘酸六胺银(periodic acid-silver metheramine,PASM)染色检查各组小鼠肾组织病理改变。结果PCR检测结果显示,成功构建lepr^(db/db)/eNos^(-/-)DKO小鼠。与同窝对照组相比,DKO小鼠的体质量、血糖水平与饮水进食量均显著高于同窝对照小鼠。DKO小鼠的尿白蛋白与尿白蛋白排泄率显著高于WT小鼠。病理学结果显示,DKO小鼠的肾小球体积明显增大,系膜基质增生明显。结论基于CRISPR/Cas9基因编辑技术可成功构建lepr^(db/db)/eNos^(-/-)DKO小鼠,DKO小鼠可反映糖尿病肾病的典型表现,为深入研究糖尿病肾病的作用机制提供动物模型。

A review of the literature on the use of CRISPR/Cas9 gene therapy to treat hepatocellular carcinoma

Noncoding RNAs instruct the Cas9 nuclease to site speifillyl cleave DNA in the CRISPR/Cas9 system.Despite the high incidence of hepatocellular carcinoma(HCC),the patient's outcome is poor.As a result of the emergence of therapeutic resistance in HCC patients,dlinicians have faced difficulties in treating such tumor.In addition,CRISPR/Cas9 screens were used to identify genes that improve the dlinical response of HCC patients.It is the objective of this article to summarize the current understanding of the use of the CRISPR/Cas9 system for the treatment of cancer,with a particular emphasis on HCC as part of the current state of knowledge.Thus,in order to locate recent developments in oncology research,we examined both the Scopus database and the PubMed database.The ability to selectively interfere with gene expression in combinatorial CRISPR/Cas9 screening can lead to the discovery of new effective HCC treatment regimens by combining clinically approved drugs.Drug resistance can be overcome with the help of the CRISPR/Cas9 system.HCC signature genes and resistance to treatment have been uncovered by genome-scale CRISPR activation screening although this method is not without limitations.It has been extensively examined whether CRISPR can be used as a tool for disease research and gene therapy.CRISPR and its applications to tumor research,particularly in HCC,are examined in this study through a review of the literature.

On the Impairment of Stress-Induced Changes in Triglyceride Levels via a Sub-Toxic Dose of Unmethylated Cytidine Phosphate Guanosine Oligodinucleotide (a Toll-Like Receptor 9 Ligand)

Changes in lipid metabolism have been implicated in protection against infectious diseases. In the first experiment of this study, we measured clinical lipid parameters in a murine model where the unmethylated cytidine phosphate guanosine (CpG) oligodinucleotide (ODN1826), a Toll-like receptor 9 (TLR9) agonist was administered in combination with D-galactosamine (GalN) that caused relatively liver-specific inflammation and toxicity. In the control mice group injected with phosphate-buffered saline (PBS) (acute psychological stress model associated with blood sampling), the serum triglyceride (TG) levels showed a rapid decrease followed by a rebound at 24 h as we have recently reported. However, such a TG rebound was impaired in the CpG/GalN- and solely CpG-treated groups of mice despite an absence of liver injury based on serum alanine aminotransferase levels in the latter group. Thus, the stress-associated serum TG rebound was abrogated by the injection of a sub-hepatotoxic CpG dose. In the second experiment, we simply measured the hepatic CD36 and SACRB1 (the gene for scavenger receptor B1 (SR-B1)) transcripts after the i.p. administration of PBS, CpG or CpG/GalN. There was a remarkable elevation of hepatic CD36 transcript expression in both the CpG- and CpG/GalN-treated mice at 8 h post-CpG injection whereas the increase in the PBS-treated mice was slower than the former two groups, suggesting that hepatic CD36 transcript expression is more pronounced in the combined stress models than under psychological stress alone. The individual mice data showed that the increase in CD36 expression was accompanied by a reduction in SCARB1 mRNA, showing reciprocal regulation between these two genes. Together with our previously reported findings, these data suggest that, in a murine model combining psychological stress with TLR-triggered hepatic inflammation, the psychological stress facilitates liver uptake of plasma TG (and its components fatty acids), but the subsequent re-esterification and/or release of TG-rich lipoproteins from the liver is impaired due to the concomitant TLR-signaling. We hypothesize that lipid metabolism during acute stress shifts toward an elevated hepatic uptake of lipids due to concomitant TLR signaling, facilitating the clearance of bacterial lipids by the liver.

Generation of double knockout cattle via CRISPR-Cas9 ribonucleoprotein(RNP)electroporation

Background Genome editing has been considered as powerful tool in agricultural fields.However,genome editing progress in cattle has not been fast as in other mammal species,for some disadvantages including long gestational periods,single pregnancy,and high raising cost.Furthermore,technically demanding methods such as microinjection and somatic cell nuclear transfer(SCNT)are needed for gene editing in cattle.In this point of view,electroporation in embryos has been risen as an alternative.Results First,editing efficiency of our electroporation methods were tested for embryos.Presence of mutation on embryo was confirmed by T7E1 assay.With first combination,mutation rates for MSTN and PRNP were 57.6%±13.7%and 54.6%±13.5%,respectively.In case of MSTN/BLG,mutation rates were 83.9%±23.6%for MSTN,84.5%±18.0%for BLG.Afterwards,the double-KO embryos were transferred to surrogates and mutation rate was identified in resultant calves by targeted deep sequencing.Thirteen recipients were transferred for MSTN/PRNP,4 calves were delivered,and one calf underwent an induction for double KO.Ten surrogates were given double-KO embryos for MSTN/BLG,and four of the six calves that were born had mutations in both genes.Conclusions These data demonstrated that production of genome edited cattle via electroporation of RNP could be effectively applied.Finally,MSTN and PRNP from beef cattle and MSTN and BLG from dairy cattle have been born and they will be valuable resources for future precision breeding.

Inactivated H9N2 vaccines developed with early strains do not protect against recent H9N2 viruses:Call for a change in H9N2 control policy

H9N2 virus has been widely distributed in wild birds and poultry around the world since its first emergence in the United States of America in 1966(Gu et al.2017;Carnaccini and Perez 2020).The virus appeared in chickens in China in the early 1990s,and over the last two decades has gradually become the dominant epidemic subtype(Sun and Liu 2015;Bi et al.2020).Although H9N2 virus infection alone cannot cause severe disease or death in poultry,H9N2 virus-infected birds experience a degree of egg production drop and can be easily infected by other pathogens,thus causing economic losses for poultry industry.

A simple and efficient CRISPR/Cas9 system permits ultra-multiplex genome editing in plants

The development and maturation of the CRISPR/Cas genome editing system provides a valuable tool for plant functional genomics and genetic improvement.Currently available genome-editing tools have a limited number of targets,restricting their application in genetic research.In this study,we developed a novel CRISPR/Cas9 plant ultra-multiplex genome editing system consisting of two template vectors,eight donor vectors,four destination vectors,and one primer-design software package.By combining the advantages of Golden Gate cloning to assemble multiple repetitive fragments and Gateway recombination to assemble large fragments and by changing the structure of the amplicons used to assemble sg RNA expression cassettes,the plant ultra-multiplex genome editing system can assemble a single binary vector targeting more than 40 genomic loci.A rice knockout vector containing 49 sg RNA expression cassettes was assembled and a high co-editing efficiency was observed.This plant ultra-multiplex genome editing system advances synthetic biology and plant genetic engineering.

CRISPR/Cas9-mediated knockout of E4 gene promotes maturation in soybean

Soybean is a broadly popular and extensively cultivated crop,however,many high-yield and high-quality varieties require specific growth conditions,restricting their widespread adoption.The appropriate light conditions and photoperiod must be attained for these varieties to thrive in new environments.In this study,we employed CRISPR/Cas9 to design two sgRNAs aimed at knocking out the maturity-related gene E4 in a major American soybean variety called''Jack'',which belongs to maturity group MGII.E4 gene is primarily involved in the photoperiodic flowering and maturity in soybean,making it an ideal candidate for genetic manipulation.We successfully obtained 1 homozygous E4-SG1 mutant type with 1-bp insertion,and 4 homozygous E4-SG2 mutants type with 2-bp deletion,7-bp deletion,61-bp deletion,and 1-bp insertion,respectively.The homozygous e4 mutant plants contained early termination codons devoid of transgenic elements.Additionally,no potential offtarget sites of the E4 gene were detected.A comparative analysis revealed that,unlike the wild-type,the maturity time of homozygous e4 mutants was early under both short-day and long-day conditions.These mutants offer novel germplasm resources that may be used to modify the photoperiod sensitivity and maturity of soybean,enhancing its adaptability to high-latitude regions.

Knock-in of exogenous sequences based on CRISPR/Cas9 targeting autosomal genes and sex chromosomes in the diamondback moth,Plutella xylostella

Genetic pest control strategies based on precise sex separation and only releasing sterile males can be accomplished by site-specific genome editing.In the current study,we showed that the mutation of single-allele Pxfl(2)d can significantly impair the normal mating behavior and testis development in male adults of the notorious cruciferous insect pest Plutella xylostella,in addition to its known functions in the ovarian development in female adults and egg hatching.Subsequent CRISPR/Cas9-based knock-in experiments revealed that site-specific integration of an exogenous green fluorescent protein(GFP)gene into autosomal Pxfl(2)d for labelling mutants could be achieved.However,this gene is not a suitable target for GFP insertion to establish a genetically stable knock-in strain because of the severe decline in reproductive capacity.We further screened for the W-chromosome-linked and Z-chromosome-linked regions to test the knock-in efficiency mediated by CRISPR/Cas9.The results verified that both types of chromosomes can be targeted for the site-specific insertion of exogenous sequences.We ultimately obtained a homozygous knock-in strain with the integration of both Cas9 and cyan fluorescent protein(CFP)expression cassettes on a Z-linked region in P.xylostella,which can also be used for early sex detection.By injecting the sgRNA targeting Pxfl(2)d alone into the eggs laid by female adults of the Z-Cas9-CFP strain,the gene editing efficiency reached 29.73%,confirming the success of expressing a functional Cas9 gene.Taken together,we demonstrated the feasibility of the knock-in of an exogenous gene to different genomic regions in P.xylostella,while the establishment of a heritable strain required the positioning of appropriate sites.This study provides an important working basis and technical support for further developing genetic strategies for insect pest control.

Combining prognostic value of serum carbohydrate antigen 19-9 and tumor size reduction ratio in pancreatic ductal adenocarcinoma

BACKGROUND Pancreatic ductal adenocarcinoma(PDAC)is a common cancer with increasing morbidity and mortality due to changes of social environment.AIM To evaluate the significance of serum carbohydrate antigen 19-9(CA19-9)and tumor size changes pre-and post-neoadjuvant therapy(NAT).METHODS This retrospective study was conducted at the Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment,Chongqing University Cancer Hospital.This study specifically assessed CA19-9 levels and tumor size before and after NAT.RESULTS A total of 156 patients who completed NAT and subsequently underwent tumor resection were included in this study.The average age was 65.4±10.6 years and 72(46.2%)patients were female.Before survival analysis,we defined the post-NAT serum CA19-9 level/pre-NAT serum CA19-9 level as the CA19-9 ratio(CR).The patients were divided into three groups:CR<0.5,CR>0.5 and<1 and CR>1.With regard to tumor size measured by both computed tomography and magnetic resonance imaging,we defined the post-NAT tumor size/pre-NAT tumor size as the tumor size ratio(TR).The patients were then divided into three groups:TR<0.5,TR>0.5 and<1 and TR>1.Based on these groups divided according to CR and TR,we performed both overall survival(OS)and disease-free survival(DFS)analyses.Log-rank tests showed that both OS and DFS were significantly different among the groups according to CR and TR(P<0.05).CR and TR after NAT were associated with increased odds of achieving a complete or near-complete pathologic response.Moreover,CR(hazard ratio:1.721,95%CI:1.373-3.762;P=0.006),and TR(hazard ratio:1.435,95%CI:1.275-4.363;P=0.014)were identified as independent factors associated with OS.CONCLUSION This study demonstrated that post-NAT serum CA19-9 level/pre-NAT serum CA19-9 level and post-NAT tumor size/pre-NAT tumor size were independent factors associated with OS in patients with PDAC who received NAT and subsequent surgical resection.

Two-dimensional layered In_(2)P_(3)S_(9): A novel superior anode material for sodium-ion batteries

Developing reliable and efficient anode materials is essential for the successfully practical application of sodium-ion batteries.Herein,employing a straightforward and rapid chemical vapor deposition technique,two-dimensional layered ternary indium phosphorus sulfide(In_(2)P_(3)S_(9)) nanosheets are prepared.The layered structure and ternary composition of the In_(2)P_(3)S_(9) electrode result in impressive electrochemical performance,including a high reversible capacity of 704 mA h g^(-1) at 0.1 A g^(-1),an outstanding rate capability with 425 mA h g^(-1) at 5 A g^(-1),and an exceptional cycling stability with a capacity retention of88% after 350 cycles at 1 A g^(-1).Furthermore,sodium-ion full cell also affords a high capacity of 308 and114 mA h g^(-1) at 0.1 and 5 A g^(-1).Ex-situ X-ray diffraction and ex-situ high-resolution transmission electron microscopy tests are conducted to investigate the underlying Na-storage mechanism of In_(2)P_(3)S_(9).The results reveal that during the first cycle,the P-S bond is broken to form the elemental P and In_(2)S_(3),collectively contributing to a remarkably high reversible specific capacity.The excellent electrochemical energy storage results corroborate the practical application potential of In_(2)P_(3)S_(9) for sodium-ion batteries.

In silico evaluation of kuwanon compounds as antiviral agents targeting H9N2 influenza virus

Background:The threat of avian influenza a subtype avian influenza A(H9N2)virus remains a significant concern,necessitating the exploration of novel antiviral agents.This study employs network pharmacology and computational analysis to investigate the potential of kuwanons,a natural compounds against H9N2 influenza virus.Methods:Leveraging comprehensive databases and bioinformatics tools,we elucidate the molecular mechanisms underlying Kuwanons pharmacological effects against H9N2 influenza virus.Network pharmacology identifies H9N2 influenza virus targets and compounds through integrated protein-protein interaction and Kyoto Encyclopedia of Genes and Genomes analyses.Molecular docking studies were performed to assess the binding affinities and structural interactions of Kuwanon analogues with key targets,shedding light on their potential inhibitory effects on viral replication and entry.Results:Compound-target network analysis revealed complex interactions(120 nodes,163 edges),with significant interactions and an average node degree of 2.72.Kyoto Encyclopedia of Genes and Genomes analysis revealed pathways such as Influenza A,Cytokine-cytokine receptor interaction pathway in H9N2 influenza virus.Molecular docking studies revealed that the binding free energy for the docked ligands ranged between-5.2 and-9.4 kcal/mol for the human interferon-beta crystal structure(IFNB1,Protein Data Bank:1AU1)and-5.4 and-9.6 kcal/mol for Interleukin-6(IL-6,PDB:4CNI).Conclusion:Our findings suggest that kuwanon exhibits promising antiviral activity against H9N2 influenza virus by targeting specific viral proteins,highlighting its potential as a natural therapeutic agent in combating avian influenza infections.

MAP3K9通过上调Notch-1促进胰腺癌细胞的增殖与迁移

目的:探讨MAP3K9通过调控Notch-1促进胰腺癌细胞增殖、迁移的机制。方法:在胰腺癌细胞中分别转染MAP3K9过表达质粒和siRNA,RT-qPCR检测MAP3K9 mRNA表达水平,MTT实验检测转染后细胞增殖能力的改变,流式细胞术检测细胞凋亡能力的变化,划痕试验检测细胞迁移能力的变化,Transwell实验检测细胞的迁移与侵袭能力,Western Blot检测MAP3K9、Notch-1及EMT相关蛋白的表达情况。结果:RT-qPCR和Western Blot显示,PaTu-8988和PANC-1细胞的MAP3K9表达水平低于BXPC-3细胞;RT-qPCR结果表明,转染MAP3K9过表达质粒可以显著提高PaTu-8988和PANC-1细胞MAP3K9 mRNA表达水平,而转染siRNA MAP3K9可明显下调BXPC-3细胞MAP3K9 mRNA表达水平;上调胰腺癌细胞MAP3K9表达,可提高胰腺癌细胞增殖、迁移与侵袭能力,并抑制细胞凋亡;在胰腺癌细胞中过表达MAP3K9,可上调Notch-1、Vimentin、N-cadherin以及slug蛋白表达水平,并降低E-cadherin表达水平。结论:MAP3K9能够激活Notch-1,进而促进胰腺癌细胞的上皮—间充质转化(EMT)过程,增强胰腺癌细胞增殖及迁移能力。

The combined detection of carcinoembryonic antigen,carcinogenic antigen 125,and carcinogenic antigen 19-9 in colorectal cancer patients

BACKGROUND Hepatic metastases are common and difficult to treat after colorectal cancer(CRC)surgery.The predictive value of carcinoembryonic antigen(CEA),cancer antigen(CA)125 and CA19-9 combined tests for liver metastasis is unclear.AIM To evaluate predictive value of combined tests for CEA,CA125,and CA19-9 levels in patients with liver metastases of CRC.METHODS The retrospective study included patients with CRC alone(50 cases)and patients with CRC combined with liver metastases(50 cases)who were hospitalized between January 2021 and January 2023.Serum CEA,CA125 and CA19-9 levels were compared between the two groups,and binary logistic regression was used to analyze the predictive value of the combination of these tumor markers in liver metastasis.In addition,we performed receiver operating characteristic(ROC)curve analysis to assess its diagnostic accuracy.RESULTS The results showed that the serum CEA,CA125 and CA19-9 levels in the CRC with liver metastasis group were significantly higher than those in the CRC alone group.Specifically,the average serum CEA level in the CRC with liver metastasis group was 162.03±810.01 ng/mL,while that in the CRC alone group was 5.71±9.76 ng/mL;the average serum CA125 levels were 43.47±83.52 U/mL respectively.and 13.5±19.68 U/mL;the average serum CA19-9 levels were 184.46±473.13 U/mL and 26.55±43.96 U/mL respectively.In addition,binary logistic regression analysis showed that CA125 was significant in predicting CRC liver metastasis(P<0.05).ROC curve analysis results showed that the areas under the ROC curves of CEA,CA125 and CA19-9 were 0.607,0.692 and 0.586.CONCLUSION These results suggest that combined detection of these tumor markers may help early detection and intervention of CRC liver metastasis,thereby improving patient prognosis.

Long non-coding RNA VPS9D1-AS1对乳腺癌细胞恶性行为的影响和机制

目的探讨长链非编码RNA(LncRNA)VPS9D1-AS1对乳腺癌细胞恶性行为的影响和机制。方法收集49例接受手术的乳腺癌患者的乳腺癌组织和癌旁组织,体外培养人正常乳腺上皮细胞MCF-10A和乳腺癌细胞系MCF-7、T47D、BT549,采用实时荧光定量PCR(RT-qPCR)检测miR-4695-5p及LncRNA VPS9D1-AS1表达水平;选择MCF-7细胞分别转染si-NC、si-LncRNA VPS9D1-AS1、pcDNA、pcDNA-LncRNA VPS9D1-AS1、miR-NC、miR-4695-5p模拟物、anti-miR-NC+si-LncRNA VPS9D1-AS1、anti-miR-4695-5p+si-LncRNA VPS9D1-AS1,采用RT-qPCR检测MCF-7细胞中LncRNA VPS9D1-AS1、miR-4695-5p表达水平,CCK-8和Transwell实验评估细胞存活率和迁移侵袭数,蛋白质印记法检测IL-6、MMP2、MMP9蛋白水平;双荧光素酶实验证实LncRNA VPS9D1-AS1与miR-4695-5p的靶向关系。结果LncRNA VPS9D1-AS1在乳腺癌组织和MCF-7、T47D、BT549细胞系中表达上调(P<0.05),miR-4695-5p表达下调(P<0.05),MCF-7细胞中LncRNA VPS9D1-AS1、miR-4695-5p变化最明显,选择MCF-7细胞进行后续实验;转染LncRNA VPS9D1-AS1后,MCF-7细胞存活率、细胞迁移和侵袭数以及IL-6、MMP2、MMP9蛋白水平降低(P<0.05);转染miR-4695-5p模拟物后,miR-4695-5p表达升高(P<0.05),MCF-7细胞存活率、细胞迁移和侵袭数及IL-6、MMP2、MMP9蛋白水平降低(P<0.05);转染pcDNA-LncRNA VPS9D1-AS1后,MCF-7细胞中miR-4695-5p表达下降(P<0.05);共转染anti-miR-4695-5p+si-LncRNA VPS9D1-AS1后,MCF-7细胞存活率、迁移数和侵袭数及IL-6、MMP2、MMP9蛋白水平升高(P<0.05)。结论干扰LncRNA VPS9D1-AS1通过靶向上调miR-4695-5p抑制促炎因子IL-6表达,进而抑制乳腺癌MCF-7细胞增殖、迁移及侵袭。

Serum tumor markers (carcinoembryonic antigen, carbohydrate antigen 19-9, carbohydrate antigen 72-4, carbohydrate antigen 24-2, ferritin) and gastric cancer prognosis correlation

BACKGROUND Gastric cancer is a kind of malignant tumor which is prevalent all over the world.Although some progress has been made in the treatment of gastric cancer,its prognosis is still not optimistic,so it is of great significance to find reliable prog-nostic indicators to guide the treatment and management of patients with gastric cancer.AIM To explore the relationship between serum levels of five biomarkers[carcinoem-bryonic antigen(CEA),carbohydrate antigen(CA)19-9,CA72-4,CA24-2,and ferritin]and prognosis in patients with gastric cancer.METHODS This study included 200 patients with gastric adenocarcinoma,and conducted an in-depth analysis of their baseline characteristics,relationship between tumor markers and staging,and prognosis.The study found that CA19-9 has a signi-ficant correlation with tumor stage,the average levels of CA24-2,CEA,CA72-4 and ferritin were slightly increased disregarding the stage of tumor.Survival analysis showed that increases in CEA,CA19-9,CA24-2,and ferritin were all associated with shortened overall survival of patients.Further multivariate ana-lysis revealed that elevated serum CA72-4 levels were an inde-pendent adverse prognostic factor.RESULTS This study reveals that there is a significant correlation between the expression levels of serum tumor markers CEA,CA19-9,CA72-4,CA24-2 and ferritin in patients with gastric cancer and prognosis,and can be used as important indicators for prognostic evaluation of gastric cancer.In particular,markers that appear abnormally elevated initially may help identify gastric cancer patients with poor prognosis.CONCLUSION Serum CEA and CA19-9 play an important role in the prognosis assessment of gastric cancer,and are effective tools to guide clinical practice and optimize individualized treatment strategies for gastric cancer patients.

薄皮甜瓜新品种“蜜脆9号”的选育

“蜜脆9号”是以‘HC3’作母本,‘PI6’作父本杂交育成的优质抗病丰产薄皮甜瓜新品种。植株长势强健,果实直筒形,平均单果质量500~550 g,果面灰白覆有墨绿条带,果肉绿色,中心可溶性固形物含量14%~16%,耐贮运。全生育期103~108 d,果实发育期30~35 d,抗病、抗逆性较强。适于陕西、河北、山东、内蒙古等地区保护地栽培。

耐热型西番莲品种“钦蜜9号”花器官发育特征与繁育系统研究

为明确耐热型黄果西番莲品种“钦蜜9号”花器官发育进程特性和繁育系统类型,测定其花器官表型性状、花粉活性、柱头可授性、异交指数和花粉胚珠比。结果表明,“钦蜜9号”花器官发育进程为现蕾期—花冠发育期—雌雄蕊发育期—裂蕾期—开花授粉期—谢花期,时间持续25~27 d,开花时间为下午13:00—15:00,单花开放时长约24 h,开花前3 d左右(花药即将开裂时)至裂蕾时柱头可授性最强;花粉数量为7.94×10^(5)个/花药,活性为90.11%,繁育系统类型为异交型,自交亲和,异交需要传粉者。这些特征为“钦蜜9号”35℃以上高温还能正常开花结果提供重要参考条件。