| Literature DB >> 27866851 |
Anna Rita Cantelmo1, Lena-Christin Conradi1, Aleksandra Brajic1, Jermaine Goveia1, Joanna Kalucka1, Andreas Pircher1, Pallavi Chaturvedi2, Johanna Hol3, Bernard Thienpont4, Laure-Anne Teuwen1, Sandra Schoors1, Bram Boeckx4, Joris Vriens5, Anna Kuchnio1, Koen Veys1, Bert Cruys1, Lise Finotto1, Lucas Treps1, Tor Espen Stav-Noraas3, Francesco Bifari1, Peter Stapor1, Ilaria Decimo1, Kim Kampen1, Katrien De Bock1, Guttorm Haraldsen3, Luc Schoonjans1, Ton Rabelink6, Guy Eelen1, Bart Ghesquière7, Jalees Rehman8, Diether Lambrechts4, Asrar B Malik2, Mieke Dewerchin1, Peter Carmeliet9.
Abstract
Abnormal tumor vessels promote metastasis and impair chemotherapy. Hence, tumor vessel normalization (TVN) is emerging as an anti-cancer treatment. Here, we show that tumor endothelial cells (ECs) have a hyper-glycolytic metabolism, shunting intermediates to nucleotide synthesis. EC haplo-deficiency or blockade of the glycolytic activator PFKFB3 did not affect tumor growth, but reduced cancer cell invasion, intravasation, and metastasis by normalizing tumor vessels, which improved vessel maturation and perfusion. Mechanistically, PFKFB3 inhibition tightened the vascular barrier by reducing VE-cadherin endocytosis in ECs, and rendering pericytes more quiescent and adhesive (via upregulation of N-cadherin) through glycolysis reduction; it also lowered the expression of cancer cell adhesion molecules in ECs by decreasing NF-κB signaling. PFKFB3-blockade treatment also improved chemotherapy of primary and metastatic tumors.Entities:
Keywords: angiogenesis; chemotherapy; glycolysis; metastasis; tumor endothelial cell metabolism; tumor vessel normalization
Mesh:
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Year: 2016 PMID: 27866851 PMCID: PMC5675554 DOI: 10.1016/j.ccell.2016.10.006
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743