缺氧导致的病理性血管再生与肿瘤迁移.ppt

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1、Hypoxia-induced pathological angiogenesis mediates tumor cell dissemination,invasion,and metastasis in a zebrafish tumor model,HypoxiaVEGFAngiogenesisMetastasis,概要Mechanisms underlying pathological angiogenesis in relation to hypoxia in tumor invasion and metastasis remain elusive.Tumor microvascula

2、r networks possess several unique pathological features including extremely high densities of leaky,tortuous,and primitive microvessels that usually lack pericyte coverage,base-ment membrane,and arteriole-venule distinctions.Although hypoxia often results in necrosis of the central core of a fast-gr

3、owing tumor,it could potentially persuade tumor cells to invade neighboring healthy vasculatures for survival,eventually leading to metastasis,which is one of the hallmarks for cancer therapy.,A clinical detectable metastatic mass often represents an ultimate consequence of several distinctive steps

4、 of the metastatic cascade,including dissemination of malignant cells from the primary site,transport of tumor cells via the circulation or lymphatic system,adhesion of tumor cells in distal tissues/organs,and re-growth of tumor cells into a detectable mass.Clinical detection of a metastasis does no

5、t reveal early events of tumor cell dissemination and intimate interactions between tumor cells and microvessels.So the the cancer therapy is difficult.,We have developed a zebrash tumor model that allows us to study the role of pathological angiogenesis under normoxia and hypoxia in arbitrating ear

6、ly events of the metastatic cascade at the single cell level.Hypoxia and VEGF signaling pathway significantly contribute to early events of the metastatic cascade.The ndings also shed light on molecular mechanisms of benecial effects of clinically available anti-VEGF drugs for cancer therapy.,方法和结果1

7、 Hypoxic Metastasis Model in ZebrafishThe Tg(fli1:EGFP)zebrafish embryos Murine T241 tumor cells were labeled with DiI dye in vitro and labeled cells were injected into the perivitelline cavity of 48 h post-fertilization embryos.Tumor-bearing zebrafish embryos were placed in either normoxic or hypox

8、ic water(7.5%air saturation),and monitor daily in living zebrafish embryos.,At day 3 after implantation,murine T241 tumor cells under hypoxia were significantly disseminated away from primary sites.the sizes of primary tumors in both groups remained similar.The border of primary tumors under hypoxia

9、 was irregular and invasive fronts were often present.A substantial number of tumor cells under hypoxia were disseminated to distal parts of the fish body,including the head and tail regions.Consistent with increase of tumor cell dissemination,hypoxia significantly stimulated neovascularization and

10、tortuosity of the tumor vasculature.,we also studied hypoxia induced tumor cell dissemination and metastasis in another murine tumor cell line,Lewis lung carcinoma(LLC).Increasing of tumor dissemination was well correlated with enhanced tumor neovascularization,2 Dissemination and Metastasis of Huma

11、n Tumor Cells we selected highly metastatic MDAMB-231 breast cancer and lowly metastaticOVCAR8 ovarian cancer cell lines.Implantation of MDA MB-231breast cancer cells in zebrafish embryos resulted in widespread tumor cell dissemination and metastasis at day 6 post-injection.all MDA MB-231 tumor cell

12、s were spread away from the primary site.,The difference of metastatic potentials between these two cell lines is due to their different capacities of dissemination.Thus,this zebrafish model might be used to discriminate highly and lowly metastatic potentials of human cancers and to predict prognosi

13、s.,3 Tumor-Derived VEGF Facilitates Dissemination and MetastasisT241 tumor cells were stably transfected to express VEGF at a high level.Total numbers of disseminated tumor cells and the maximal distance of metastasis in the T241-VEGF group were significantly greater than those in controls.Microvess

14、el density in T241-VEGF tumors was significantly higher relative to control tumors.At day 2 after implantation,a significant number of tumor cells invaded the neighboring tissues around primary tumors.At day 4,increasing numbers of invasive tumor cells were detected and were disseminated to distal p

15、arts of the fish body.,To generalize these findings to other tumor types,murine LLC were also stably transfected with VEGF.Similar to T241 fibrosarcoma,implantation of LLC-VEGF tumors resulted in marked increase of tumor cell dissemination,invasion and distal metastasis compared with vector controls

16、.,4 VEGF Blockade Inhibits VEGF-Tumor Cell Invasion,Dissemination,and MetastasisT241-VEGF tumor-bearing embryos were treated with sunitinib,a known VEGFR blockadeIt showed that tumor cell dissemination,metastasis and vessel density in primary tumors were significantly inhibited by sunitinib in a dos

17、e-dependent manner.the average size of primary tumors was also significantly reduced by sunitinib treatment.sunitinib effectively inhibited tumor cell dissemination and metastasis in LLC tumors,5 Inhibition of Tumor Cell Invasion,Dissemination,and Metastasis by VEGFR-2 MorpholinosA specific morpholi

18、no against VEGFR-2,a functional receptor for VEGF-induced angiogenesis,was microinjected into developing zebrafish embryos.Administration of high dosages of VEGFR-2 morpholinos resulted in early death of zebrafish embryos owing to the essential role of VEGF in development of embryonicvasculatures as

19、 seen in mice.At a relatively low concentration(0.1 mM),the VEGFR-2 morpholino selectively blocked tumor angiogenesis without significantly impairing development of physiological vascular networks,suggesting that the tumor vasculature was more susceptible to VEGF inhibition.,6 VEGFR Blockade Effecti

20、vely Blocks Hypoxia-Induced Tumor Angiogenesis and Metastasis Sunitinib virtually completely blocked the hypoxia-induced T241 tumor cell invasion,dissemination and metastasis,inhibited tumor neovascularizationHypoxia-induced malignant cell invasion,dissemination,and metastasis are mediated by VEGF-i

21、nduced pathological blood vessels.,讨论Early detection of malignant tumors is essential for curative therapy.However,cancer metastasis can occur at the very early stage of malignant diseases and in a substantial number of cases metastatic disease is the first sign of cancer whereas primary tumors rema

22、in undetectableMolecular mechanisms underlying the early onset of cancer metastasis are complex,The role of angiogenesis in tumor cell dissemination has not been well-described in mammalian tumor models.To recapitulate early steps of clinical metastasis,we develop a zebrafish metastatic model that a

23、llows us to monitor dissemination of single tumor cells from primary sites in the living body.The transparent nature of zebrafish embryos allows us to monitor tumor development and dissemination in vivo without any invasive operation;,EGFP positive vasculature in fli1:EGFPzebrafish embryos further p

24、ermit us to study tumor cell dissemination in relation to development of angiogenic vessels;Zebrafish could easily be placed in hypoxic water to study the role of tissue hypoxia in facilitating tumor cell dissemination and metastasis;Assessment of anti-metastatic effects of orally active drugs;Morph

25、olino for reverse genetics by silencing host gene functions involving angiogenesis and metastasis,How does VEGF-induced angiogenesis facilitate tumor cell invasion and metastasis?One possibility is that VEGF induces disorganized,leaky and tortuous vasculatures,which are susceptible for malignant cel

26、l invasion.In support of this hypothesis,increases of vascular density and tortuosity have been observed in our zebrafish model.The other possible mechanism is that outgrowth of blood vessels in tumors promotes intimate interactions between malignant and endothelial cells and the latter provides nic

27、hes for tumor cell invasion and metastasis.Additionally,perfusion of VEGF-induced vessels could act as a chemoattractant for tumor cell migration and eventually lead to tumor cell invasion along the vascular system.,Inhibition of tumor angiogenesis might prevent metastasis.Inversely,recent reports s

28、how that antiangiogenic drugs for treatment of established animal tumors lead to invasion and metastasis.The difference between these findings and our data could be due to the sizes of primary tumors.In an established tumor,anti-VEGF drugs could generate tissue hypoxia,leading to an invasive and met

29、astatic phenotype.In zebrafish tumor model,primary tumors remain in situ as tiny nodules and antiangiogenic drugs would not result in significant hypoxia as in a well-established tumor.Thus,tumor sizes might be a key determinant for antiangiogenic drug-produced therapeutic benefits or tumor cell inv

30、asion and metastasis.,A substantial number of patients are diagnosed for malignant diseases owing to metastasis as the first sign of cancer.Primary tumors remain undetectable using conventional techniques,suggesting that dissemination of tumor cells occurs at the very early stage.Thus,our results shed light on early metastatic processes by visualizing single cell invasion and metastasis in the living body without invasive procedures.,