搜索到655篇“ LYN“的相关文章
Aspartoacylase suppresses prostate cancer progression by blocking LYN activation
2024年
Background:Globally,despite prostate cancer(PCa)representing second most prevalent malignancy in male,the precise molecular mechanisms implicated in its pathogenesis remain unclear.Consequently,elucidating the key molecular regulators that govern disease progression could substantially contribute to the establishment of novel therapeutic strategies,ultimately advancing the management of PCa.Methods:A total of 49 PCa tissues and 43 adjacent normal tissues were collected from January 2017 to December 2021 at Zhongnan Hospital of Wuhan University.The advanced transcriptomic methodologies were employed to identify differentially expressed mRNAs in PCa.The expression of aspartoacylase(ASPA)in PCa was thoroughly evaluated using quantitative real-time PCR and Western blotting techniques.To elucidate the inhibitory role of ASPA in PCa cell proliferation and metastasis,a comprehensive set of in vitro and in vivo assays were conducted,including orthotopic and tumor-bearing mouse models(n=8 for each group).A combination of experimental approaches,such as Western blotting,luciferase assays,immunoprecipitation assays,mass spectrometry,glutathione S-transferase pulldown experiments,and rescue studies,were employed to investigate the underlying molecular mechanisms of ASPA's action in PCa.The Student‘s t-test was employed to assess the statistical significance between two distinct groups,while one-way analysis of variance was utilized for comparisons involving more than two groups.A two-sided P<0.05 was deemed to indicate statistical significance.Results:ASPA was identified as a novel inhibitor of PCa progression.The expression of ASPA was found to be significantly down-regulated in PCa tissue samples,and its decreased expression was independently associated with patients’prognosis(HR=0.60,95%CI 0.40–0.92,P=0.018).Our experiments demonstrated that modulation of ASPA activity,either through gain-or loss-of-function,led to the suppression or enhancement of PCa cell proliferation,migration,and invasion,respectively.The inhib
Hong WengKang-Ping XiongWang WangKai-Yu QianShuai YuanGang WangFang YuJun LuoMeng‑Xin LuZhong‑Hua YangTao LiuXing HuangHang ZhengXing-Huan Wang
关键词:LYNAP-1C-JUNPHOSPHORYLATION
短周期相接双星LX Lyn和V0853 Aur的周期变化研究
统计研究表明,宇宙中大部分的恒星以双星或聚星的形式存在。双星的观测研究能够帮助我们更好地理解恒星的形成和演化规律,有助于深入了解宇宙的发展史。其中,W UMa型相接双星(contact binaries,CBs)是密近双...
张旭
关键词:光变曲线
一种基于LYN基因鉴定鸭体重性状的分子标记和应用
本发明涉及一种基于LYN基因鉴定鸭体重性状的分子标记和应用,属于分子标记检测技术领域,所述分子标记的核苷酸序列由SEQ ID NO.1所示的LYN基因序列的第1279位多态性位点及其上下游碱基组成,SEQ ID NO.1...
金四华邱桂如孙娜何云侠耿照玉郭立平王玮琪陈文静唐嘉欣
Periodic Variation Studies of the Two Short Period W UMa-type Eclipsing Binaries: LX Lyn and V0853 Aur
2024年
In this paper,new light curves(LCs) of contact eclipsing binary(CEB) systems LX Lyn and V0853 Aur are presented and analyzed by using the 2015 version of the Wilson-Devinney(W-D) code.In order to explain their asymmetric LCs,cool starspots on the components were employed.It is suggested that their fill-out degrees are f=12.0%(LX Lyn) and f=26.3%(V0853 Aur).At the same time,we found that LX Lyn is a W-type eclipsing binary(EB) with an orbital inclination of i=84°.88 and a mass ratio of q=2.31.V0853 Aur is also a W-type CEB with a mass ratio of q=2.77 and an orbital inclination of i= 79°.26.Based on all available times of light minimum,their orbital period changes are studied by using the O-C method.The O-C diagram of LX Lyn reveals a cyclic oscillation with a period of about 14.84 yr and an amplitude of 0.0019 days,which can be explained by the light-travel time effect(LTTE) due to the presence of a third body with a minimum mass of0.06M_⊙.For V0853 Aur,it is discovered that the O-C diagram of the system also shows a cyclic oscillation with a period of 9.64 yr and an amplitude of 0.03365 days.The cyclic oscillation of V0853 Aur can be attributed to the LTTE by means of a third body with a mass no less than 3.77M_⊙.The third body may play an important role in the formation and evolution of these systems.
Xu ZhangBin Zhang
鞋底(LYN-23006)
1.本外观设计产品的名称:鞋底(LYN‑23006)。;2.本外观设计产品的用途:本外观产品设计用于鞋底。;3.本外观设计产品的设计要点:在于形状。;4.最能表明设计要点的图片或照片:立体图。
吴敏
miR-496通过调控 LYN对胃癌细胞增殖和凋亡的影响
2023年
目的研究miR-496在胃癌细胞中的表达情况, 并探讨其在胃癌细胞增殖和凋亡过程中的作用及机制。方法实时荧光定量PCR(qPCR)检测miR-496在正常胃上皮细胞株和胃癌细胞系AGS、MKN45中的的表达情况。在表达水平最低的AGS细胞中敲低miR-496, 同时设置阴性对照组和空白对照组。分别用CCK8实验和流式细胞仪检测细胞增殖和凋亡。使用生物信息学软件筛选出miR-496的靶基因LYN, QPCR检测转染miR-496对LYN表达的影响, 随后进行了Rescure拯救实验, 进一步研究miR-496通过调控LYN对胃癌细胞的作用机制。利用GraphPad Prism 9软件进行数据分析, 计量资料以均数±标准差(±s)表示, 组间比较采用t检验。结果 miR-496在AGS、MKN45中表达显著低于胃正常上皮细胞(P<0.05)。通过转染过表达miR-496后, 可以抑制AGS细胞的增殖, 同时可以使AGS细胞的凋亡比例明显升高(P<0.05)。qPCR结果显示, miR-496过表达组能够抑制LYN的表达(P<0.05)。生物信息学分析显示, miR-496与LYN激酶(LYN) 3’UTR区域结合, 通过过表达miR-496可抑制AGS细胞中LYN的表达, 而CCK8拯救实验显示过表达LYN能够解除miR-496对细胞增殖的抑制作用;流式凋亡检测显示表达LYN能够解除miR-496对细胞凋亡的促进作用(P<0.05)。结论 miR-496在胃癌细胞中低表达, 其通过靶向胃癌细胞中LYN的表达抑制胃癌细胞的增殖, 促进胃癌细胞的凋亡。
苏锐李英健朱志达赵恩宏
关键词:胃肿瘤细胞增殖细胞凋亡
IP Lyn:A Totally Eclipsing Contact Binary with an Extremely Low Mass Ratio
2023年
We present the first photometric and orbital period investigations for a neglected totally eclipsing contact binary IP Lyn.The photometric solutions derived from both ground-based and several surveys'observations suggest that it is a shallow contact binary with an extremely low mass ratio of 0.055.The weak asymmetry observed in our multiple band light curves can be interpreted as a result of an active cool spot on the primary.The absolute physical parameters were determined with the Gaia-distance-based method and checked by an empirical relation.Combining the eclipse timings collected from the literature and those derived from our and variable surveys'observations,we find that IP Lyn has been undergoing a secular orbital period increase for the past two decades,implying a mass transfer from the less massive secondary to the primary.By comparing the current parameters with the critical instability ones,we infer that IP Lyn is currently stable in spite of its relatively low mass ratio and orbital angular momentum.Finally,from a catalog of 117 extremely low mass ratio contact binaries,we find that their orbital angular momenta are significantly lower than those of the contact binaries with a relatively high mass ratio,suggesting they should be at the late evolutionary stage of a contact binary.
Zi-Xuan YinZi-Bin MengPei-Ru WuXu-Dong ZhangYun-Xia YuKe HuFu-Yuan Xiang
苦参碱通过抑制Lyn/Syk信号通路治疗大鼠过敏性哮喘被引量:2
2023年
目的探讨苦参碱(Mat)调节Lyn/Syk信号通路对过敏性哮喘大鼠免疫功能的影响。方法随机取12只SD大鼠作为对照组(NC组),其余大鼠参考先前文献通过卵清蛋白(OVA)造模。将造模成功的过敏性哮喘大鼠随机平分为Model组、Mat组(100 mg/kg Mat)、MLR-1023组(30 mg/kg Lyn/Syk信号通路激活剂MLR-1023)、Mat+MLR-1023组(100 mg/kg Mat+30 mg/kg MLR-1023),每组12只。NC组、Model组给予等量的生理盐水,每天1次,持续4周。收集支气管肺泡灌洗液(BALF)并进行嗜酸粒细胞计数;ELISA试剂盒检测血清和BALF液中细胞因子水平;HE染色检测肺组织病理变化;测定肺组织中组胺水平;Western blot检测Lyn/Syk通路相关蛋白水平。结果NC组大鼠肺组织染色清晰,结构正常。Model组出现大量炎性细胞浸润现象,支气管周围嗜酸粒细胞增多,上皮细胞增大、脱落。Model组较NC组血清中TNF-α、IL-4、IL-5、IL-1β和LTD-4水平,BALF中IgE、OVA sIgE、嗜酸粒细胞数量以及肺组织p-Lyn/Lyn、p-Syk/Syk、组胺水平均显著增加(P<0.05);与Model组相比,Mat组嗜酸粒细胞数量、TNF-α、IL-4、IL-5、IL-1β和LTD-4水平、IgE、OVA sIgE、组胺、p-Lyn/Lyn、p-Syk/Syk水平均显著降低(P<0.05),而MLR-1023组结果与Mat组趋势相反;MLR-1023消除了Mat对过敏性哮喘大鼠的治疗效果。结论Mat可能通过下调Lyn/Syk信号通路对过敏性哮喘大鼠免疫功能起到改善作用。
范爱欣袁菲唐科毅
关键词:苦参碱过敏性哮喘免疫功能
茯苓酸调节Lyn/Syk信号通路对哮喘大鼠气道炎症的影响
2023年
目的探讨茯苓酸对支气管哮喘大鼠气道炎症及酪氨酸蛋白激酶(Lyn)/脾酪氨酸激酶(Syk)信号通路的影响及其机制。方法建立支气管哮喘大鼠模型,将大鼠分为对照组、哮喘组、Lyn抑制剂PP2组、茯苓酸5 mg/kg组及茯苓酸10 mg/kg组,观察大鼠肺组织病理学变化,并进行炎症评分。ELISA法检测支气管肺泡灌洗液(BALF)与血清TNF-α、IFN-γ、IL-4水平,Giemsa染色法检测BALF炎症细胞,qRT-PCR法检测肺组织Lyn、Syk、STAT3 mRNA表达水平,Western blot检测肺组织Lyn、Syk、p-STAT3蛋白表达。结果哮喘组大鼠支气管黏膜水肿,管腔内容物增多,微血管渗漏,并伴有大量炎性细胞浸润。与对照组比较,哮喘组大鼠支气管炎症评分、BALF中炎性细胞数目、血清及BALF中TNF-α、IL-4水平及肺组织Lyn、Syk、STAT3mRNA及蛋白表达水平显著升高,BALF中IFN-γ水平显著降低(P<0.05);与哮喘组比较,PP2组、茯苓酸5 mg/kg组与茯苓酸10 mg/kg组的上述改变均得以减轻(P<0.05),且茯苓酸10 mg/kg组比茯苓酸5 mg/kg组效果为明显(P<0.05)。结论茯苓酸可抑制支气管哮喘大鼠气道炎症反应,其机制可能与抑制Lyn/Syk信号通路有关。
王艳梅甘德堃赵润杨梁彦昌
关键词:茯苓酸气道炎症
Lyn对支气管哮喘早期气道重塑的影响及作用机制研究
研究目的:支气管哮喘(以下简称哮喘)是儿童呼吸系统最常见疾病之一。随着全球气候环境的变化,哮喘发病率逐年增高,成为严重危害社会公共健康的重大问题。哮喘由各种环境因素和变应原诱发,逐渐形成慢性气道炎症,且伴随黏液高分泌、不...
张琴珍
关键词:LYNPI3K/AKT

相关作者

邵建国
作品数:169被引量:496H指数:10
供职机构:南通大学
研究主题:表达及意义 非酒精性脂肪性肝病 基因多态性 原发性肝癌 肝细胞癌
李民
作品数:102被引量:262H指数:7
供职机构:南通市第三人民医院
研究主题:胃肠激素 加味瓜蒌散 中医药疗法 退高黄汤 门静脉压力
陈琳
作品数:116被引量:254H指数:6
供职机构:南通大学
研究主题:注意缺陷多动障碍 事件相关电位 原发性肝癌 肝细胞肝癌 肝癌
何红梅
作品数:12被引量:16H指数:3
供职机构:南通市第三人民医院
研究主题:LYN 非酒精性脂肪性肝炎 护肝 HCK SSECKS
苏锐
作品数:32被引量:59H指数:4
供职机构:承德医学院附属医院
研究主题:大肠腺癌 大肠癌组织 GALECTIN-3 免疫组织化学 CLUSTERIN