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1.
Int J Cancer ; 147(4): 1206-1214, 2020 08 15.
Article in English | MEDLINE | ID: mdl-31922252

ABSTRACT

Tumor vasculature is innately dysfunctional. Poorly functional tumor vessels inefficiently deliver chemotherapy to tumor cells; vessel hyper-permeability promotes chemotherapy delivery primarily to a tumor's periphery. Here, we identify a method for enhancing chemotherapy efficacy in Ewing sarcoma (ES) in mice by modulating tumor vessel permeability. Vessel permeability is partially controlled by the G protein-coupled Sphinosine-1-phosphate receptors 1 and 2 (S1PR1 and S1PR2) on endothelial cells. S1PR1 promotes endothelial cell junction integrity while S1PR2 destabilizes it. We hypothesize that an imbalance of S1PR1:S1PR2 is partially responsible for the dysfunctional vascular phenotype characteristic of ES and that by altering the balance in favor of S1PR1, ES vessel hyper-permeability can be reversed. In our study, we demonstrate that pharmacologic activation of S1PR1 by SEW2871 or inhibition of S1PR2 by JTE-013 caused more organized, mature and functional tumor vessels. Importantly, S1PR1 activation or S1PR2 inhibition improved antitumor efficacy. Our data suggests that pharmacologic targeting of S1PR1 and S1PR2 may be a useful adjuvant to standard chemotherapy for ES patients.


Subject(s)
Bone Neoplasms/drug therapy , Doxorubicin/pharmacology , Oxadiazoles/pharmacology , Pyrazoles/pharmacology , Pyridines/pharmacology , Sarcoma, Ewing/drug therapy , Sphingosine-1-Phosphate Receptors/antagonists & inhibitors , Thiophenes/pharmacology , Animals , Antibiotics, Antineoplastic/pharmacology , Bone Neoplasms/metabolism , Capillary Permeability/drug effects , Cell Line, Tumor , Endothelial Cells/drug effects , Endothelial Cells/metabolism , Humans , Mice, Nude , Sarcoma, Ewing/metabolism , Sphingosine 1 Phosphate Receptor Modulators/pharmacology , Sphingosine-1-Phosphate Receptors/metabolism , Treatment Outcome , Xenograft Model Antitumor Assays/methods
2.
PLoS One ; 12(4): e0173488, 2017.
Article in English | MEDLINE | ID: mdl-28403177

ABSTRACT

This study describes the genetic diversity and population structure of 194 native maize populations from 23 countries of Latin America and the Caribbean. The germplasm, representing 131 distinct landraces, was genetically characterized as population bulks using 28 SSR markers. Three main groups of maize germplasm were identified. The first, the Mexico and Southern Andes group, highlights the Pre-Columbian and modern exchange of germplasm between North and South America. The second group, Mesoamerica lowland, supports the hypothesis that two separate human migration events could have contributed to Caribbean maize germplasm. The third, the Andean group, displayed early introduction of maize into the Andes, with little mixing since then, other than a regional interchange zone active in the past. Events and activities in the pre- and post-Columbian Americas including the development and expansion of pre-Columbian cultures and the arrival of Europeans to the Americas are discussed in relation to the history of maize migration from its point of domestication in Mesoamerica to South America and the Caribbean through sea and land routes.


Subject(s)
Genetic Variation , Zea mays/genetics , Central America , Gene Frequency , Genes, Plant , Microsatellite Repeats , Phylogeny , Sequence Analysis, DNA , South America , West Indies
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