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Evaluation of encapsulated cell movement in a heterogeneous,sedimentary aquifer
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《Global Geology》 1998年第1期84-85,共2页
关键词 cell Evaluation of encapsulated cell movement in a heterogeneous sedimentary
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Cortactin mediated morphogenic cell movements during zebrafish (Danio rerio) gastrulation 被引量:1
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作者 YU Dan1,2, ZHANG Peijun1 & ZHAN Xi3 1. Experimental Marine Biology Lab, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China 2. Graduate School of the Chinese Academy of Sciences, Beijing 100039, China 3. Greenebaum Cancer Center, Department of Cancer Center, University of Maryland School of Medicine, MD 20855, USA 《Science China(Life Sciences)》 SCIE CAS 2005年第6期601-607,共7页
Cell migration is essential to direct embryonic cells to specific sites at which their developmental fates are ultimately determined. However, the mechanism by which cell motility is regulated in embryonic development... Cell migration is essential to direct embryonic cells to specific sites at which their developmental fates are ultimately determined. However, the mechanism by which cell motility is regulated in embryonic development is largely unknown. Cortactin, a filamentous actin binding protein, is an activator of Arp2/3 complex in the nucleation of actin cytoskeleton at the cell leading edge and acts directly on the machinery of cell motility. To determine whether cortactin and Arp2/3 mediated actin assembly plays a role in the morphogenic cell movements during the early development of zebrafish, we initiated a study of cortactin expression in zebrafish embryos at gastrulating stages when massive cell migrations occur. Western blot analysis using a cortactin specific monoclonal antibody demonstrated that cortactin protein is abundantly present in em-bryos at the most early developmental stages. Immunostaining of whole-mounted embryo showed that cortactin immunoreactivity was associated with the embryonic shield, predominantly at the dorsal side of the embryos during gastrulation. In addition, cortactin was detected in the convergent cells of the epiblast and hypoblast, and later in the central nervous system. Im-munofluorescent staining with cortactin and Arp3 antibodies also revealed that cortactin and Arp2/3 complex colocalized at the periphery and many patches associated with the cell-to-cell junction in motile embryonic cells. Therefore, our data suggest that cortactin and Arp2/3 medi-ated actin polymerization is implicated in the cell movement during gastrulation and perhaps the development of the central neural system as well. 展开更多
关键词 cortactin Arp2/3 complex zebrafish cell movements morphogenesis gastrulation neurulation.
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Gold Alloy Dental Inlay for Preventing Involuntary Body Movements Caused by Electromagnetic Waves Emitted by a Cell Phone 被引量:1
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作者 Yoshiro Fujii 《Open Journal of Antennas and Propagation》 2014年第4期37-43,共7页
Cell phone and personal computer use has increased considerably in recent years, particularly in developed countries. These devices have facilitated communication on a global scale. However, there have been a number o... Cell phone and personal computer use has increased considerably in recent years, particularly in developed countries. These devices have facilitated communication on a global scale. However, there have been a number of reports of health problems related to the electromagnetic waves emitted by such electronic devices. A long list of both general and severe symptoms, including headaches, fatigue, tinnitus, dizziness, memory loss, irregular heartbeat and whole-body skin le-sions, have been reported. These are reportedly associated with the condition known as electro-magnetic hypersensitivity (EHS). This report shows how a subject’s abnormal involuntary body movements, caused by electromagnetic waves emitted by a cell phone, are prevented by placing a gold alloy inlay in the subject’s mouth. It appears that the subject’s involuntary movements are the result of balance dysregulation resulting from EHS. The subject’s various symptoms improve after the specific dental treatment. However, the underlying mechanism of the symptoms and the rea-sons why this treatment is so successful remain unknown. Further research is required to clarify these issues. 展开更多
关键词 Balance DYSREGULATION cell PHONE Electromagnetic HYPERSENSITIVITY Involuntary Body movement
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Alterations in metastatic properties of hepatocellular carcinoma cell following H-ras oncogene transfection 被引量:48
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作者 Qing Wang~1 Zhi Ying Lin~2 Xiao Li Feng~3 ~1Department of Microbiology,Medical Center of Fudan University.the former Shanghai Medical University,Shanghai 200032,China ~2Liver Cancer Institute,Zhongshan Hospital,Shanghai 200032,China ~3Shanghai Institute of Biochemistry,Academy Sinica,Shanghai 200031,ChinaQing Wang earned master degree from Shanghai Medical University in 1996,now a senior lecturer of microbiology,specialized in the role of oncogcncs on tumor metastasis,having 8 papers published. 《World Journal of Gastroenterology》 SCIE CAS CSCD 2001年第3期335-339,共5页
AIM: To demonstrate the relationship between H-ras oncogene and hepatocellular carcinoma (HCC) metastasis. METHODS: Activated H-ras oncogene was transfected into SMMC 7721, a cell line derived from human HCC, by calci... AIM: To demonstrate the relationship between H-ras oncogene and hepatocellular carcinoma (HCC) metastasis. METHODS: Activated H-ras oncogene was transfected into SMMC 7721, a cell line derived from human HCC, by calcium phosphate transfection method. Some metastasis-related parameters were detected in vitro, including adhesion assay, migration assay, expression of collagenase IV(c IV ase) and epidermal growth factor receptor (EGFR). RESULTS: The abilities of H-ras-transfected cell clones in adhesion to laminin (LN) or fibronectin (FN), migration, c IV ase secretion increased markedly, and the expression of EGFR elevated moderately. More importantly, these alterations were consistent positively with the expression of p21, the protein product of H-ras oncogene. CONCLUSION: H-ras oncogene could induce the metastatic phenotype of HCC cell in vitro to raise its metastatic potential. 展开更多
关键词 Carcinoma Hepatocellular cell Adhesion cell movement Gelatinase A Gelatinase B Gene Expression Regulation Neoplastic Genes ras Humans In Vitro Liver Neoplasms PHENOTYPE Predictive Value of Tests Receptor Epidermal Growth Factor TRANSFECTION
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Effect of a nitric oxide synthase inhibitor NG-nitro-L-arginine methyl ester on invasion of human colorectal cancer cell line SL-174T 被引量:5
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作者 Li-Bo YU Xin-Shu Dong +2 位作者 Wen-Zhou sun Dong-Lu Zhao Yue Yang 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第40期6385-6388,共4页
AIML To investigate the effect and mechanism of action of the nitric oxide synthase (NOS) inhibitor NG-nitro-L-arginine methyl ester (L-NAME) on invasion and metastasis of human colorectal cancer cell line SL-174T... AIML To investigate the effect and mechanism of action of the nitric oxide synthase (NOS) inhibitor NG-nitro-L-arginine methyl ester (L-NAME) on invasion and metastasis of human colorectal cancer cell line SL-174T. METHODS: Human colorectal cancer cel4 line SL-174T was cultured and treated separately with four different dosages of L-NAME for 72 h, Nitric oxide (NO) production was measured with Griess reagent, The effect of L-NAME on invasion and migration of SL-174T cells were evaluated by using Transwell chambers attached with polycarbonate filters and reconstituted basement membrane (Matrigel), RT-PCR was performed to determine the mRNA levels of matrix metalloproteinase-2 (MMP-2) and tissue inhibitor metalloproteinase-2 (TIMP-2),RESULTS: L-NAME could significantly inhibit NO production of SL-174T in a dose-dependent manner. After being treated for 72 h with 0.2, 0.4, 0.8, and 1.0 mmol/L L- NAME, respectively, the ability of the L-NAME treated SL- 174T cells to invade the reconstituted basement membrane decreased significantly (t = 8.056, P〈0.05; t= 14.467, P〈0.01; t= 27.785, P〈0.01; and t= 29.405, P〈0.01, respectively) and the inhibition rates were 10.29%, 19.62%, 34.08%, and 42.23%, respectively. Moreover, L-NAME could inhibit migration of SL-174T cells, and the inhibition rates were 20.76%, 24.95%, 39.43%, and 46. 85% for L-NAME at 0.2, 0.4, 0.8, and 1.0 mmol/L, respectively (t = 15.116, P〈0.01). In addition, after treatment with L-NAME, expression of MMP-2 mRNA was significantly decreased (t = 71.238, P〈0.01) and that of TIMP-2 mRNA was markedly increased (t = -13.020, P〈0.01). CONCLUSION: L-NAME exerts anti-invasive and anti- metastatic effects on SL-174T cell line via downregulating MNP-2 mRNA expression and upregulating TIMP-2 mRNA expression. 展开更多
关键词 Colorectal Neoplasms Neoplasm Invasiveness cell Line Tumor cell movement Dose-Response Relationship Drug FEMALE Gelatinase A Humans Male NG-Nitroarginine Methyl Ester Nitric Oxide Nitric Oxide Synthase INHIBITORS Tissue Inhibitor of Metalloproteinase-2
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Effects on Proliferation and Migration of the Human Colon Carcinoma Cell Line SW620 by Silencing of Hepatocyte Growth Factor Expression
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作者 Yi-tao JIA Lei ZHANG +4 位作者 Yan LI Ya-di WANG Wei GUO Lei CAO Zhong-xin LI 《Clinical oncology and cancer researeh》 CAS CSCD 2010年第5期277-283,共7页
OBJECTIVE Hepatocyte growth factor (HGF) expression is closely related to the progression and poor prognosis of colorectal cancer patients. In this study, we investigated the effects on proliferation and migration o... OBJECTIVE Hepatocyte growth factor (HGF) expression is closely related to the progression and poor prognosis of colorectal cancer patients. In this study, we investigated the effects on proliferation and migration of the human colon carcinoma cell line SW620 by silencing HGF expression. METHODS HGF was silenced using specific HGF a/f3 siRNA. The proliferation, migration, cell cycle and ultrastructure of SW620 cells were examined. RESULTS The transfection efficiency was 70%-80%. The expression rate of HGF in the experimental group was significantly lower than that in the negative and blank control groups (P 〈 0.05). The proliferation inhibition rate in the experimental group at 24, 48, 72 and 96 h after transfection was 14.2%, 50.2%, 39.5% and 23.2%, respectively. The migratory ability of cells in the experimental group was significantly inhibited compared with that in the negative control or blank control groups (58.2% vs. 2.1% or 0%, P 〈 0.05). CONCLUSION The application of RNA interference to silence the expression of HGF in the colon carcinoma cell line SW620 effectively inhibits the proliferation and migration of tumor cells. 展开更多
关键词 RNA interference HGF protein human cellular proliferation cell movement colorectal neoplasms.
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Effect of WFDC 2 silencing on the proliferation,motility and invasion of human serous ovarian cancer cells in vitro 被引量:12
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作者 Ya-Fei Zhu Guo-Lan Gao +2 位作者 Sheng-Bo Tang Zhen-Dong Zhang Qing-Shui Huang 《Asian Pacific Journal of Tropical Medicine》 SCIE CAS 2013年第4期265-272,共8页
Objective:To investigate effect and possible mechanisms of silencing human WFDC2(HE4) gene on biological behavior changes as cell proliferation,apoplosis,movement and invasion of human serous ovarian cancer cell lin... Objective:To investigate effect and possible mechanisms of silencing human WFDC2(HE4) gene on biological behavior changes as cell proliferation,apoplosis,movement and invasion of human serous ovarian cancer cell line SKOV3.Methods:Lentiviral WFDC2 gene sequence of small interfering siRNA was stablely transfected into SKOV3 identified by Q-PCR and western-blot. Obtained SKOV3 stable strains with silenced HE4 were measured by proliferation,apoplosis, migration,and invasion.Results:Gene sequencing showed that the oligonucleotides were successfully inserted into the expected site.After silencing HE4 in the SKOV3,proliferation was significandy inhibited(P【0.05).G<sub>0</sub>/G<sub>1</sub> phase was arrested by the cell cycle(P【0.01) and capacity of the migration and invasion decreased significandy(P【0.01).Slight early apoptosis ratio and no change of late apoplosis were found without change of Caspase-3 or Bcl-2 protein.Proteins involed in ERK pathway as phosphorylated protein as p-EGFR,p- ERK decreased and protease protein involved in tissue remoding as matrix metalloproteinases MMP-9,MMP-2 and cathepsin B decreased compared with control group.Conclusions:HE4 gene plays an important role in regulating proliferation,apoptosis,migration,invasion of serous ovarian cancer cells by ERK pathway and protease system.Its role in apoptosis needs to be further explored,and it may be a potential target for serous ovarian cancer. 展开更多
关键词 WFDC2 PROTEIN HUMAN epididymal secretory PROTEIN 4 Ovarian neoplasms cell PROLIFERATION cell movement INVASION
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Study on incisional implantation of tumor cells by carbon dioxide pneumoperitoneum in gastric cancer of a murine model 被引量:2
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作者 Wang H Zheng MH +8 位作者 Zhang HB Zhu J He JR Lu AG Ji YB Zhang MJ Jiang Y Yu BM Li HW 《World Journal of Gastroenterology》 SCIE CAS CSCD 1999年第6期544-546,共3页
关键词 STOMACH NEOPLASMS COLONIC NEOPLASMS cell movement carbon dioxide PNEUMOPERITONEUM murine model
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Model acupuncture point:Bone marrow-derived stromal stem cells are moved by a weak electromagnetic field 被引量:2
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作者 Artem N Emelyanov Marina V Borisova Vera V Kiryanova 《World Journal of Stem Cells》 SCIE CAS 2016年第10期342-354,共13页
AIM To show the existence of a structural formative role of magnetic fields(MFs) with respect to biological objects by using our proposed model of an acupoint.METHODS We introduced a magnetised 10-100 μT metal rod(ne... AIM To show the existence of a structural formative role of magnetic fields(MFs) with respect to biological objects by using our proposed model of an acupoint.METHODS We introduced a magnetised 10-100 μT metal rod(needle) into culture dishes with a negatively charged working surface and observed during 24 h how cells were arranged by MFs and by electrical fields(EFs) when attached. Rat and human bone marrow-derived stromal stem cells(r BMSCs and h BMSCs), human nonadherent mononuclear blood cells, NCTCs and A172 cells, and Escherichia coli(E. coli) were evaluated. The dish containing BMSCs was defined as the model of an acupoint. r BMSCs proliferative activity affected by the needle was investigated. For investigating electromagnetic field structures, we used the gas discharge visualisation(GDV) method.RESULTS During 24 h of incubation in 50-mm culture dishes, BMSCs or the nonadherent cells accumulated into a central heap in each dish. BMSCs formed a torus(central ring) with an inner diameter of approximately10 mm only upon the introduction of the needle in the centre of the dish. The cells did not show these effects in 35- or 90-mm culture dishes or hydrophobic dishes or rectangular cuvettes. NCTCs and A172 cells showed unstable the effects and only up to two weeks after thawing. Moreover, we observed that the appearance of these effects depended on the season. In winter, BMSCs showed no the effects. GDV experiments revealed that the resonant annular illumination gradually formed from 10 to 18-20 s in polar solutions with and without cell suspension of BMSCs, NCTCs and E. coli when using circular 50-mm dishes, stimulation at 115 V and switching of the electrode poles at 1 kH z. All these data demonstrate the resonant nature of the central ring. Significant influence of MFs on the rB MSC proliferation rate was not observed.CONCLUSION BMSCs can be moved by MFs when in the presence of a constant EF and MF, when the cells are in the responsive functional state, and when there is a resonant relationship between them. 展开更多
关键词 Stem cell movement Magnetic targeting Acupuncture MODEL ACUPOINT Frizzled-related protein Biology resonance CYTOPLASM movement GLYCOCALYX
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乳腺癌细胞条件培养基对骨髓间充质干细胞生物学行为的影响
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作者 刘丹阳 李永涛 +3 位作者 张海燕 李林 刘洋 沈雷 《天津医药》 CAS 2024年第5期454-458,共5页
目的探讨MCF-7乳腺癌细胞条件培养基对骨髓间充质干细胞(BMSC)增殖、凋亡和迁移的影响及分子机制。方法正常环境下培养的BMSC为对照组,以MCF-7细胞条件培养基培养的BMSC为MCF-7条件培养基组,向MCF-7条件培养基组添加10 nmol/L GSK690693... 目的探讨MCF-7乳腺癌细胞条件培养基对骨髓间充质干细胞(BMSC)增殖、凋亡和迁移的影响及分子机制。方法正常环境下培养的BMSC为对照组,以MCF-7细胞条件培养基培养的BMSC为MCF-7条件培养基组,向MCF-7条件培养基组添加10 nmol/L GSK690693(Akt抑制剂)为Akt抑制剂组,向MCF-7条件培养基组添加10µmol/L Reparixin(CXCR1/2抑制剂)为CXCR1/2抑制剂组。MTT实验检测各组BMSC增殖情况,Annexin V-FITC/PI双标记流式细胞凋亡实验检测各组BMSC凋亡率,Transwell细胞迁移实验检测各组BMSC的迁移能力,酶联免疫吸附试验检测两种细胞培养上清液和MCF-7细胞条件培养基中白细胞介素(IL)-8蛋白含量,Western blot检测各组BMSC的蛋白激酶B(Akt)/磷酸化Akt(p-Akt)和哺乳动物雷帕霉素靶蛋白(mTOR)/磷酸化mTOR(p-mTOR)蛋白表达。结果与对照组相比,MCF-7条件培养基组BMSC的细胞增殖水平、迁移数目以及p-Akt和p-mTOR蛋白相对表达量均增高,细胞凋亡率降低(P<0.05);与MCF-7条件培养基组相比,CXCR1/2抑制剂组和Akt抑制剂组BMSC的细胞增殖水平、迁移数目以及p-Akt和p-mTOR蛋白相对表达量均降低,细胞凋亡率增加(P<0.05);MCF-7细胞条件培养基和MCF-7培养上清液中IL-8蛋白含量均较BMSC培养上清液中IL-8蛋白含量高(P<0.05)。结论MCF-7细胞条件培养基通过激活Akt-mTOR信号通路促进BMSC增殖和迁移,抑制BMSC凋亡,其中IL-8-CXCR1/2轴发挥关键作用。 展开更多
关键词 乳腺肿瘤 肿瘤微环境 细胞增殖 细胞凋亡 细胞运动 骨髓间充质干细胞
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miR-107对口腔鳞癌细胞系CAL27增殖、侵袭及迁移的影响
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作者 张晋玮 王燕 王通 《天津医药》 CAS 2024年第9期897-900,共4页
目的探讨miR-107在口腔鳞癌细胞系CAL27中的表达及其对CAL27细胞增殖、凋亡、侵袭和迁移的影响。方法采用实时荧光定量PCR检测miR-107在口腔鳞癌细胞株CAL27和人口腔上皮细胞HOEC细胞中的表达情况;脂质体转染法将miR-107 mimic和miR-107... 目的探讨miR-107在口腔鳞癌细胞系CAL27中的表达及其对CAL27细胞增殖、凋亡、侵袭和迁移的影响。方法采用实时荧光定量PCR检测miR-107在口腔鳞癌细胞株CAL27和人口腔上皮细胞HOEC细胞中的表达情况;脂质体转染法将miR-107 mimic和miR-107 NC质粒分别转染进入CAL27细胞,并分为对照(miR-107 NC)组和miR-107过表达(miR-107 mimic)组;MTT细胞增殖实验检测细胞增殖能力,流式细胞术检测细胞凋亡率,Transwell小室实验检测细胞迁移和侵袭能力。结果CAL27细胞系中miR-107的表达低于HOEC细胞。miR-107 mimic组细胞转染后24、48、72 h光密度(OD)值均低于miR-107 NC组,凋亡细胞比例高于miR-107 NC组,而侵袭和迁移细胞数少于miR-107 NC组(P<0.05)。结论上调miR-107可抑制CAL27细胞的增殖、侵袭和迁移,并促进其凋亡。 展开更多
关键词 口腔肿瘤 RNA干扰疗法 细胞增殖 肿瘤浸润 细胞运动 miR-107
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CDC20在肺腺癌组织中的表达及对肺腺癌细胞增殖和侵袭的影响研究 被引量:1
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作者 周雪芹 栾艳超 +2 位作者 赵莉 戎超超 杨娜 《中国癌症杂志》 CAS CSCD 北大核心 2024年第5期460-472,共13页
背景与目的:肺腺癌具有早期发现难、肿瘤进展快及晚期手术切除率低等特点。尽管单药免疫治疗和免疫治疗联合化疗的相关研究在改善预后、克服耐药方面已初显成效,但是大部分肺腺癌患者从中获益仍有限。因此,迫切需要寻找具有相对较高灵... 背景与目的:肺腺癌具有早期发现难、肿瘤进展快及晚期手术切除率低等特点。尽管单药免疫治疗和免疫治疗联合化疗的相关研究在改善预后、克服耐药方面已初显成效,但是大部分肺腺癌患者从中获益仍有限。因此,迫切需要寻找具有相对较高灵敏度和特异度的新型生物标志物,以改善肺腺癌患者的预后。细胞分裂周期蛋白20(cell division cycle protein 20,CDC20)参与多种肿瘤的发生、发展,但在肺腺癌中的生物学作用及机制尚未明确。本研究旨在探究CDC20在肺腺癌中的表达情况及其对肺腺癌患者预后的预测价值,并分析CDC20对肺腺癌细胞增殖和侵袭能力的影响。方法:采用免疫组织化学(immunohistochemistry,IHC)检测CDC20在肺腺癌中的表达情况并结合生物信息学和临床病理学参数分析其与预后不良的相关性。采用Kaplan-Meier生存曲线描述CDC20对肺腺癌患者术后生存率的影响,采用COX多因素回归分析影响肺腺癌患者术后生存率的独立预后因素。通过受试者工作特征曲线分析CDC20表达在肺腺癌患者中的诊断价值。采用实时荧光定量聚合酶链反应(real-time fluorescence quantitative polymerase chain reaction,RTFQ-PCR)和蛋白质印迹法(Western blot)检测人正常肺上皮细胞系BEAS-2B、人肺腺癌细胞系A549和H1299中CDC20的表达水平。细胞实验中,通过敲低肺腺癌细胞中的CDC20,分为si-NC(对照组)、si-CDC20#1(敲低组1)和si-CDC20#2(敲低组2)3个组。采用细胞计数试剂盒-8(cell counting kit-8,CCK-8)、克隆形成、transwell和划痕实验检测细胞增殖、迁移和侵袭能力。通过基因本体论(Gene Ontology,GO)功能和京都基因与基因组百科全书(Kyoto Encyclopedia of Genes and Genomes,KEGG)通路富集分析CDC20在肺腺癌中的生物学作用。通过基因集富集分析(gene set enrichment analysis,GSEA)CDC20在肺腺癌中可能的调控通路。本研究经河北省胸科医院伦理委员会批准(编号:2022051)。结果:生物信息学及IHC结果均显示,CDC20在肺腺癌组织中显著高表达(P<0.05)。生物信息学与临床参数分析结果均显示,CDC20高表达与患者预后不良相关。Kaplan-Meier生存分析和COX回归分析均显示,CDC20表达情况与患者术后生存率呈显著负相关(P<0.05)。敲低CDC20能抑制肺腺癌细胞增殖、迁移和侵袭(P<0.05)。GO功能、KEGG通路和GSEA结果均显示,CDC20与细胞周期相关。结论:CDC20在肺腺癌中高表达,CDC20高表达是肺腺癌患者不良预后的独立危险因素。CDC20能促进肺腺癌细胞增殖、迁移和侵袭。 展开更多
关键词 细胞分裂周期蛋白20 肺腺癌 细胞增殖 细胞周期 细胞运动
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Applications of stem cells in orthodontics and dentofacial orthopedics:Current trends and future perspectives 被引量:6
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作者 Shiva Safari Arezoo Mahdian Saeed Reza Motamedian 《World Journal of Stem Cells》 SCIE CAS 2018年第6期66-77,共12页
A simple overview of daily orthodontic practice involves use of brackets, wires and elastomeric modules. However, investigating the underlying effect of orthodontic forces shows various molecular and cellular changes.... A simple overview of daily orthodontic practice involves use of brackets, wires and elastomeric modules. However, investigating the underlying effect of orthodontic forces shows various molecular and cellular changes. Also, orthodontics is in close relation with dentofacial orthopedics which involves bone regeneration. In this review current and future applications of stem cells(SCs) in orthodontics and dentofacial orthopedics have been discussed. For craniofacial anomalies, SCs have been applied to regenerate hard tissue(such as treatment of alveolar cleft) and soft tissue(such as treatment of hemifacial macrosomia). Several attempts have been done to reconstruct impaired temporomandibular joint. Also, SCs with or without bone scaffolds and growth factors have been used to regenerate bone following distraction osteogenesis of mandibular bone or maxillary expansion. Current evidence shows that SCs also have potential to be used to regenerate infrabony alveolar defects and move the teeth into regenerated areas. Future application of SCs in orthodontics could involve accelerating tooth movement, regenerating resorbed roots and expanding tooth movement limitations. However, evidence supporting these roles is weak and further studies are required to evaluate the possibility of these ideas. 展开更多
关键词 Alveolar bone grafting Dentofacial DEFORMITIES Distraction osteogenesis Guided tissue regeneration ORTHODONTICS ORTHODONTIC tooth movement ORTHOGNATHIC surgery Periodontitis Root RESORPTION Stem cells
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基质金属蛋白酶7在肝癌细胞迁移及免疫细胞浸润中的作用与预后价值
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作者 刘淑岩 杨其昌 +2 位作者 沈屹 周虹 钱金锋 《临床肝胆病杂志》 CAS 北大核心 2024年第7期1420-1427,共8页
目的评估基质金属蛋白酶7(MMP7)在肝癌细胞迁移及免疫细胞浸润中的作用及预后价值。方法分别构建下调或上调靶基因MMP7的MMP7_siRNA、pMMP7转染肝癌细胞株(MHCC97H)。采用RT-qPCR、Western Blot分别检测细胞中靶基因mRNA及蛋白的表达水... 目的评估基质金属蛋白酶7(MMP7)在肝癌细胞迁移及免疫细胞浸润中的作用及预后价值。方法分别构建下调或上调靶基因MMP7的MMP7_siRNA、pMMP7转染肝癌细胞株(MHCC97H)。采用RT-qPCR、Western Blot分别检测细胞中靶基因mRNA及蛋白的表达水平。扫描电镜和Transwell小室实验分别观察细胞伪足和迁移能力的变化,并采用生物信息学的方法,在TCGA、TIMER数据库分析MMP7与免疫细胞及肝癌患者免疫浸润评分之间的相关性,并进一步研究MMP7与肝癌患者预后的相关性。相关性分析采用Spearman方法。Sanger Box在线工具评估MMP7在肝癌总体生存期、疾病特异性生存期方面的意义。Kaplan-Meier法绘制生存曲线,Log-rank检验评估不同组样本之间的预后差异。结果构建的MMP7_siRNA、pMMP7转染MHCC97H细胞后均能有效下调或上调靶基因MMP7的表达,在MHCC97H细胞中MMP7被干扰后细胞伪足明显减少,并且变短,但是过表达MMP7之后细胞表面丝状伪足数量明显增多,并且伪足长度变长,放射状排列。Transwell小室结果发现,MMP7_siRNA2能够显著降低细胞迁移能力(P<0.05),而转染pMMP7后,细胞迁移能力显著增加(P<0.05)。MMP7的表达与B淋巴细胞(r=0.37)、CD4+T淋巴细胞(r=0.40)、中性粒细胞(r=0.49)、巨噬细胞(r=0.49)、树突状细胞(r=0.47)显著相关(P值均<0.05)。在TCGA数据库中,基于总体生存期最佳截断值将肝癌患者分成MMP7高表达组(n=267)和MMP7低表达组(n=146),结果发现,MMP7高表达组的总体生存期明显低于MMP7低表达组(P<0.05);基于疾病特异性生存期最佳截断值将肝癌患者分成MMP7高表达组(n=257)和MMP7低表达组(n=145),结果发现,MMP7高表达组的疾病特异性生存期也低于MMP7低表达组(P<0.05)。结论MMP7促进了肝癌细胞的迁移,并在免疫细胞浸润中发挥主要作用,MMP7的表达也与肝癌的预后具有明显相关性。 展开更多
关键词 肝肿瘤 基质金属蛋白酶7 细胞运动
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CXCL12通过CXCR4/AKT诱导自噬对肺癌细胞迁移的作用
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作者 张一帆 万里新 +1 位作者 李慧 孙晓 《青岛大学学报(医学版)》 CAS 2024年第5期669-672,共4页
目的探究外源性趋化因子配体12(CXCL12)通过激活趋化因子受体4(CXCR4)/蛋白激酶B(AKT)信号通路对肺癌细胞迁移的作用。方法用外源性CXCL12处理肺癌细胞,通过Western blot实验对自噬相关蛋白LC3B以及CXCR4/AKT信号通路蛋白进行检测,通过... 目的探究外源性趋化因子配体12(CXCL12)通过激活趋化因子受体4(CXCR4)/蛋白激酶B(AKT)信号通路对肺癌细胞迁移的作用。方法用外源性CXCL12处理肺癌细胞,通过Western blot实验对自噬相关蛋白LC3B以及CXCR4/AKT信号通路蛋白进行检测,通过划痕实验对细胞的迁移进行检测。结果与对照组相比较,加入外源性CXCL12组细胞的迁移能力增强(t=3.949,P<0.05),自噬相关蛋白LC3BⅡ的表达水平显著增高(t=3.051,P<0.05),CXCR4的表达和AKT的磷酸化水平也明显增高(t=2.974、4.307,P<0.05)。结论CXCL12可能通过CXCR4/AKT信号通路诱导自噬进而促进肺癌细胞的迁移。 展开更多
关键词 趋化因子CXCL12 受体 CXCR4 肺肿瘤 自噬 细胞运动
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LINC01140过表达对肺腺癌细胞H1975增殖和侵袭的影响
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作者 崔玉洁 张洁 +3 位作者 张立晓 魏亚红 刘苗苗 陈连刚 《临床误诊误治》 CAS 2024年第21期73-78,共6页
目的探讨LINC01140过表达对肺腺癌细胞H1975增殖及侵袭的影响,以为靶向药物的选择和预后评估提供依据。方法基于生物信息学结果,选取表皮生长因子受体(EGFR)T790M突变阳性的肺腺癌细胞株H1975,通过转染技术构建LINC01140过表达细胞系,... 目的探讨LINC01140过表达对肺腺癌细胞H1975增殖及侵袭的影响,以为靶向药物的选择和预后评估提供依据。方法基于生物信息学结果,选取表皮生长因子受体(EGFR)T790M突变阳性的肺腺癌细胞株H1975,通过转染技术构建LINC01140过表达细胞系,分为对照组(H1975/NC)、高表达组(H1975/LINC01140),RT⁃PCR检测细胞系中LINC01140的表达水平。对2组细胞进行培养,用MTS检测细胞的增殖能力,平板划痕试验检测细胞迁移能力,Transwell试验检测细胞侵袭能力。结果通过数据库得知LINC01140在肺癌组织中的表达低于癌旁组织,且与临床特征及生存均有关(P<005)。同时,本研究结果证实成功构建LINC01140过表达H1975细胞系。与H1975/NC比较,H1975/LINC01140中LINC01140表达水平升高,细胞吸光度、迁移率增高,穿膜细胞数增多(P<005)。结论LINC01140过表达可促进肺腺癌细胞H1975的增殖、迁移和侵袭,检测其表达水平可指导临床靶向药物的选择,提高疗效,从而改善预后。 展开更多
关键词 肺肿瘤 LINC01140 H1975 细胞增殖 细胞运动 肿瘤侵润
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基于改进RRT的清扫机器人全覆盖路径规划 被引量:1
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作者 孔滕广 高焕兵 陈修贤 《计算机工程与应用》 CSCD 北大核心 2024年第13期311-318,共8页
针对钢筋轧制车间中大型非结构化环境下清扫机器人在全覆盖路径规划时所面临的算法运行成本高、避障性能差和区域覆盖率低等问题,提出了一种利用单元分解法分区覆盖和融合跳点搜索法的RRT区域转移的全覆盖路径规划算法。利用MCD(movemen... 针对钢筋轧制车间中大型非结构化环境下清扫机器人在全覆盖路径规划时所面临的算法运行成本高、避障性能差和区域覆盖率低等问题,提出了一种利用单元分解法分区覆盖和融合跳点搜索法的RRT区域转移的全覆盖路径规划算法。利用MCD(movement cell decomposition)算法实现自由区域覆盖,为了解决区域间路径规划时的避障问题,引入融合跳点搜索策略的RRT算法,通过增加节点扩展的导向性,使其更偏向目标区域进行搜索,并利用贪婪算法裁剪冗余点修正路径以及三次B样条曲线法平滑处理。通过仿真与实验验证了算法在不同环境下的可行性和有效性,相比于其他方法所规划的路径更短且大大降低了路径重复率,提高了机器人避障效率的同时实现了全区域路径覆盖。 展开更多
关键词 单元分解 融合改进RRT算法 清扫机器人 MCD局部覆盖算法 全覆盖路径规划
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盐酸双吗啡肽对耐药食管癌细胞迁移和侵袭能力的影响
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作者 石晓丽 苏治国 +4 位作者 张英 杨国帅 彭温暖 王晨 马霖 《精准医学杂志》 2024年第6期547-551,共5页
目的 探讨骨形态发生蛋白(BMP)小分子抑制剂盐酸双吗啡肽(Dorsomorphin)对耐药食管癌EC109/PTX细胞迁移和侵袭能力的影响。方法 MTT实验检测不同浓度盐酸双吗啡肽对EC109/PTX细胞增殖的影响并确定后续实验的浓度。以筛选出的1μmol/L盐... 目的 探讨骨形态发生蛋白(BMP)小分子抑制剂盐酸双吗啡肽(Dorsomorphin)对耐药食管癌EC109/PTX细胞迁移和侵袭能力的影响。方法 MTT实验检测不同浓度盐酸双吗啡肽对EC109/PTX细胞增殖的影响并确定后续实验的浓度。以筛选出的1μmol/L盐酸双吗啡肽的浓度作为试验组,同时设立空白对照组,处理EC109/PTX细胞48 h。采用流式细胞仪检测盐酸双吗啡肽对EC109/PTX细胞凋亡的影响。采用划痕实验和Transwell实验检测两组EC109/PTX细胞的迁移和侵袭能力。采用Western blotting实验检测两组EC109/PTX细胞中Vimentin、E-cadherin、N-cadherin蛋白相对表达水平。结果 1μmol/L盐酸双吗啡肽对EC109/PTX细胞的细胞抑制率为(9.89±1.12)%。培养第48小时时,对照组和实验组EC109/PTX细胞的凋亡率比较差异无显著性(P>0.05)。划痕实验和Transwell实验显示,与对照组相比,实验组EC109/PTX细胞的迁移率和细胞穿膜率显著降低(t=85.42、19.65,P<0.05)。Western blotting实验显示,与对照组相比,实验组细胞中Vimentin、N-cadherin蛋白相对表达量显著降低(t=19.40、41.79,P<0.05),N-cadherin蛋白表达量显著增高(t=58.12,P<0.05)。结论 BMP抑制剂盐酸双吗啡肽能影响耐药食管癌细胞中EMT相关蛋白表达,从而抑制耐药肿瘤细胞的迁移和侵袭。 展开更多
关键词 骨形态发生蛋白质4 Dorsomorphin 抗药性 肿瘤 食管肿瘤 细胞运动 肿瘤浸润 上皮-间质转化 基因表达调控 肿瘤
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慢性饥饿应激通过增强ITGB1表达促进结直肠癌细胞迁移 被引量:1
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作者 李思雨 曹静桦 王凤伟 《肿瘤防治研究》 CAS 2024年第4期240-248,共9页
目的探讨慢性饥饿应激对结直肠癌细胞增殖、迁移能力的影响及其机制。方法采用长期血清饥饿法模拟肿瘤细胞慢性饥饿环境,通过梯度降低血清浓度构建结直肠癌SW480、DLD-1低血清耐受亚株并观察细胞形态的改变;利用CCK-8和Transwell实验检... 目的探讨慢性饥饿应激对结直肠癌细胞增殖、迁移能力的影响及其机制。方法采用长期血清饥饿法模拟肿瘤细胞慢性饥饿环境,通过梯度降低血清浓度构建结直肠癌SW480、DLD-1低血清耐受亚株并观察细胞形态的改变;利用CCK-8和Transwell实验检测长期血清饥饿后细胞增殖、迁移能力的改变;对SW480细胞正常血清培养株和血清饥饿细胞亚株进行转录组测序,并对差异基因进行GO功能、KEGG通路富集分析;利用String数据库和Metascape软件构建迁移相关核心蛋白关联网络,并选取16个核心基因进行RT-qPCR验证;检测ITGB1及其相关通路关键分子在蛋白水平的表达;敲降ITGB1和使用STAT3抑制剂后利用Transwell实验检测血清饥饿组和对照组SW480细胞迁移能力的变化。结果长期血清饥饿减弱了SW480细胞的增殖能力,但增强其迁移能力;而对DLD-1细胞的增殖和迁移能力均产生抑制作用。SW480细胞转录组数据分析发现长期血清饥饿诱导细胞中3016个基因表达上调,其中迁移相关差异基因有283个;Metascape 分析发现ITGB1、CD44、TNS1、STAT3等潜在核心基因相 互关联;经验证,长期血清饥饿导致SW480细胞中VTN、 TNS1、VEGFA、STAT3、ITGB1等基因的mRNA水平显著上 调,同时导致ITGB1、MMP2等的蛋白水平和JAK2、STAT3 的磷酸化水平显著上调;敲降ITGB1和使用STAT3抑制剂 均能减弱长期血清饥饿SW480细胞的迁移能力。结论 结 直肠癌细胞可耐受慢性饥饿应激,并且该种应激可通过上 调ITGB1表达促进结直肠癌细胞的迁移能力。 展开更多
关键词 饥饿 结直肠瘤 细胞运动 整合素Β1 STAT3转录因子
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顺铂联合衣霉素对神经母细胞瘤的抑制作用及其机制
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作者 张腾龙 孙文静 +1 位作者 宋军莹 侯琳 《精准医学杂志》 2024年第4期283-288,共6页
目的探究顺铂(DDP)联合衣霉素(TM)对人神经母细胞瘤SH-SY5Y及SK-N-SH细胞的抑制作用及其机制。方法将人神经母细胞瘤SH-SY5Y及SK-N-SH细胞分为对照组、TM组(0.4mg/LTM处理24h)、DDP组(4mg/LDDP处理24h)和DDP+TM组(0.4mg/LTM+4mg/LDDP共... 目的探究顺铂(DDP)联合衣霉素(TM)对人神经母细胞瘤SH-SY5Y及SK-N-SH细胞的抑制作用及其机制。方法将人神经母细胞瘤SH-SY5Y及SK-N-SH细胞分为对照组、TM组(0.4mg/LTM处理24h)、DDP组(4mg/LDDP处理24h)和DDP+TM组(0.4mg/LTM+4mg/LDDP共处理24h)。采用CCK-8实验、平板克隆实验、划痕实验、Transwell实验分别检测各组细胞的细胞活力、增殖能力、迁移能力和侵袭能力,采用免疫印迹法检测各组细胞中JAK2-STAT3-HIF1α通路相关蛋白JAK-2、p-JAK2、STAT3、p-STAT3和HIF1α的表达水平。结果实验结果显示,DDP+TM组两种细胞的细胞活力、增殖能力、侵袭能力、第12及24小时时的迁移能力及JAK2-STAT3-HIF1α通路各蛋白表达水平均显著低于其他三组(tLSD=2.14~78.95,P<0.05)。结论DDP联合TM可通过JAK2-STAT3-HIF1α通路抑制神经母细胞瘤的增殖和迁移,该结果为神经母细胞瘤的治疗提供了新思路。 展开更多
关键词 神经母细胞瘤 顺铂 衣霉素 JANUS激酶2 STAT3转录因子 缺氧诱导因子1 Α亚基 细胞运动 细胞增殖
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