dc.creator | Naipauer, Julian | |
dc.creator | Rosario, Santas | |
dc.creator | Gupta, Sachin | |
dc.creator | Premer, Courtney | |
dc.creator | Méndez Solís, Omayra | |
dc.creator | Schlesinger, Mariana | |
dc.creator | Ponzinibbio, Maria Virginia | |
dc.creator | Jain, Vaibhav | |
dc.creator | Gay, Lauren | |
dc.creator | Renne, Rolf | |
dc.creator | Chan, Ho Lam | |
dc.creator | Morey, Lluis | |
dc.creator | Salyakina, Daria | |
dc.creator | Abba, Martín Carlos | |
dc.creator | Williams, Sion | |
dc.creator | Hare, Joshua M. | |
dc.creator | Goldschmidt Clermont, Pascal | |
dc.creator | Mesri, Enrique Alfredo | |
dc.date.accessioned | 2021-02-22T17:01:03Z | |
dc.date.accessioned | 2022-10-15T04:08:28Z | |
dc.date.available | 2021-02-22T17:01:03Z | |
dc.date.available | 2022-10-15T04:08:28Z | |
dc.date.created | 2021-02-22T17:01:03Z | |
dc.date.issued | 2019-12-27 | |
dc.identifier | Naipauer, Julian; Rosario, Santas; Gupta, Sachin; Premer, Courtney; Méndez Solís, Omayra; et al.; PDGFRA defines the mesenchymal stem cell Kaposi's sarcoma progenitors by enabling KSHV oncogenesis in an angiogenic environment; Public Library of Science; Plos Pathogens; 15; 12; 27-12-2019; 1-38 | |
dc.identifier | 1553-7366 | |
dc.identifier | http://hdl.handle.net/11336/126251 | |
dc.identifier | 1553-7374 | |
dc.identifier | CONICET Digital | |
dc.identifier | CONICET | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/4343527 | |
dc.description.abstract | Kaposi’s sarcoma (KS) is an AIDS-defining cancer caused by the KS-associated herpesvirus (KSHV). Unanswered questions regarding KS are its cellular ontology and the conditions conducive to viral oncogenesis. We identify PDGFRA(+)/SCA-1(+) bone marrow-derived mesenchymal stem cells (Pα(+)S MSCs) as KS spindle-cell progenitors and found that pro-angiogenic environmental conditions typical of KS are critical for KSHV sarcomagenesis. This is because growth in KS-like conditions generates a de-repressed KSHV epigenome allowing oncogenic KSHV gene expression in infected Pα(+)S MSCs. Furthermore, these growth conditions allow KSHV-infected Pα(+)S MSCs to overcome KSHV-driven oncogene-induced senescence and cell cycle arrest via a PDGFRA-signaling mechanism; thus identifying PDGFRA not only as a phenotypic determinant for KS-progenitors but also as a critical enabler for viral oncogenesis. | |
dc.language | eng | |
dc.publisher | Public Library of Science | |
dc.relation | info:eu-repo/semantics/altIdentifier/url/https://dx.plos.org/10.1371/journal.ppat.1008221 | |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1371/journal.ppat.1008221 | |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | KSHV | |
dc.subject | PDGFRA | |
dc.subject | Mesenchymal stem cell | |
dc.subject | Angiogenic environment | |
dc.title | PDGFRA defines the mesenchymal stem cell Kaposi's sarcoma progenitors by enabling KSHV oncogenesis in an angiogenic environment | |
dc.type | info:eu-repo/semantics/article | |
dc.type | info:ar-repo/semantics/artículo | |
dc.type | info:eu-repo/semantics/publishedVersion | |