000142883 001__ 142883 000142883 005__ 20240229112533.0 000142883 0247_ $$2doi$$a10.3389/fnins.2018.01004 000142883 0247_ $$2pmid$$apmid:30686972 000142883 0247_ $$2pmc$$apmc:PMC6335617 000142883 0247_ $$2ISSN$$a1662-453X 000142883 0247_ $$2ISSN$$a1662-4548 000142883 0247_ $$2altmetric$$aaltmetric:54070040 000142883 037__ $$aDKFZ-2019-00513 000142883 041__ $$aeng 000142883 082__ $$a610 000142883 1001_ $$0P:(DE-He78)5ba5b48bd126214d9cb66291fa4ae303$$aBreckwoldt, Michael$$b0$$eFirst author 000142883 245__ $$aCorrelated MRI and Ultramicroscopy (MR-UM) of Brain Tumors Reveals Vast Heterogeneity of Tumor Infiltration and Neoangiogenesis in Preclinical Models and Human Disease. 000142883 260__ $$aLausanne$$bFrontiers Research Foundation$$c2019 000142883 3367_ $$2DRIVER$$aarticle 000142883 3367_ $$2DataCite$$aOutput Types/Journal article 000142883 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1613568432_15951 000142883 3367_ $$2BibTeX$$aARTICLE 000142883 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000142883 3367_ $$00$$2EndNote$$aJournal Article 000142883 520__ $$aDiffuse tumor infiltration into the adjacent parenchyma is an effective dissemination mechanism of brain tumors. We have previously developed correlated high field magnetic resonance imaging and ultramicroscopy (MR-UM) to study neonangiogenesis in a glioma model. In the present study we used MR-UM to investigate tumor infiltration and neoangiogenesis in a translational approach. We compare infiltration and neoangiogenesis patterns in four brain tumor models and the human disease: whereas the U87MG glioma model resembles brain metastases with an encapsulated growth and extensive neoangiogenesis, S24 experimental gliomas mimic IDH1 wildtype glioblastomas, exhibiting infiltration into the adjacent parenchyma and along white matter tracts to the contralateral hemisphere. MR-UM resolves tumor infiltration and neoangiogenesis longitudinally based on the expression of fluorescent proteins, intravital dyes or endogenous contrasts. Our study demonstrates the huge morphological diversity of brain tumor models regarding their infiltrative and neoangiogenic capacities and further establishes MR-UM as a platform for translational neuroimaging. 000142883 536__ $$0G:(DE-HGF)POF3-314$$a314 - Tumor immunology (POF3-314)$$cPOF3-314$$fPOF III$$x0 000142883 588__ $$aDataset connected to CrossRef, PubMed, 000142883 7001_ $$0P:(DE-HGF)0$$aBode, Julia$$b1 000142883 7001_ $$0P:(DE-He78)a1f4b408b9155beb2a8f7cba4d04fe88$$aSahm, Felix$$b2 000142883 7001_ $$0P:(DE-He78)d9984bb7c7ce85fffd8c63899fb1d7fa$$aKrüwel, Thomas$$b3 000142883 7001_ $$0P:(DE-He78)aceff95b461bf57aaa3c92ea45b28233$$aSolecki, Gergely$$b4 000142883 7001_ $$aHahn, Artur$$b5 000142883 7001_ $$0P:(DE-He78)7f9dda5a1b9a9ffc384598e80ade05f9$$aWirthschaft, Peter$$b6 000142883 7001_ $$0P:(DE-He78)5b87d282e810365cc9599b1384318145$$aBerghoff, Anna S$$b7 000142883 7001_ $$aHaas, Maximilian$$b8 000142883 7001_ $$0P:(DE-HGF)0$$aVenkataramani, Varun$$b9 000142883 7001_ 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