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ID:33734355
大小:366.37 KB
页数:42页
时间:2019-02-28
《重组人血管内皮抑制素yh-16联合放射治疗对肺腺癌a549移植瘤的抑制作用与机制分析》由会员上传分享,免费在线阅读,更多相关内容在行业资料-天天文库。
1、华中科技大学硕士学位论文(12.20±1.11)%、(14.75±0.91)%、(16.48±0.85)%、(20.52±1.89)%、(24.45±1.48)%,(P<0.01)。放疗+Endostar组bFGFmRNA表达水平和VEGF表达水平明显低于对照组、Endostar组和放疗组。结论1.Endostar明显提高了放射治疗对肺腺癌A549移植瘤的疗效,其机制与Endostar通过下调bFGF转录水平和VEGF表达水平抑制肿瘤新生血管的形成、协同-1放射治疗促进肿瘤细胞凋亡相关。2.DDP(3mg·kg
2、,d3)联合放射治疗治疗肺腺癌-1-1A549移植瘤和Endostar(10mg·kg·d,d1-14)联合放射治疗疗效相当。关键词肺肿瘤;重组人血管内皮抑制素;放射治疗;移植瘤;人肺腺癌细胞系A549;碱性成纤维细胞生长因子;血管内皮生长因子4华中科技大学硕士学位论文TheInhibitionofRh-endostatin(YH-16)inCombinationwithRadiotherapyonLungAdenocarcinomaA549inMiceanditsMechanismsGraduateWuHui
3、-TaSupervisorProf.ChenYuanTongjiHospitalCancerCenter,TongjiMedicalCollege,HuazhongUniversityofScienceandTechnology,Wuhan430030ABSTRACTObjectiveThemajorgoalofthisstudywastoevaluatetheinhibitoryeffectofEndostarincombinationwithradiotherapyonlungadenocarcinomaA
4、549inBALB/cnudemice.Meanwhile,theratesoftumorcellapoptosisandthelevelsofbFGFmRNAandVEGFexpressionweredetectedtoresearchtheinteractionmechanismsofcombinedtherapy.Inaddition,acomparisonbetweentheeffectofEndostarplusradiotherapyandcisplatinplusradiotherapyonA54
5、9lungadenocarcinomamodelswascarriedout.MethodsThetransplantationtumormodelsofA549lungadenocarcinomawereestablished.Allmicewererandomizedinto5groups(n=6)whenthelargestdiameterof-1tumorreachesat1.0cm.Endostargroup:miceweregiven10mg·kgofEndostardailybyperitonea
6、linjectionfor14days.Controlgroup:miceweregivenbyequalvolumesofnormalsodiumfor14day.Radiotherapygroup:miceweretreatedby10Gyelectronbeamirradiationatthethirdday.Endostarplusradiotherapygroup:miceweregivendailyby-1peritonealinjectionwith10mg·kgofEndostarfor14da
7、y,inaddition,theyweregiven10Gyelectronbeamirradiationatthethirdday.DDPplusradiotherapygroup:twohoursbeforemiceweregiven10Gyelectronbeamirradiationatthethirdday,theyweregiven-13mg·kgcisplatinbyperitonealinjection.Wemeasuredthelargestdiameterandthevertical5华中科
8、技大学硕士学位论文thdiameteroftumoratdifferenttimepoints.Atthe16day,allmicewereexecuted.Thetumorswereappliedtoanalysisofratesoftumorcellapoptosis,andtheexpressionlevelsofbFGFmRNAbyRT-PCRandVEGFbyIHCwerea
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