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Targeting glioblastoma-derived pericytes improves chemotherapeutic outcome.


ABSTRACT: Glioblastoma is the most common malignant brain cancer in adults, with poor prognosis. The blood-brain barrier limits the arrival of several promising anti-glioblastoma drugs, and restricts the design of efficient therapies. Recently, by using state-of-the-art technologies, including thymidine kinase targeting system in combination with glioblastoma xenograft mouse models, it was revealed that targeting glioblastoma-derived pericytes improves chemotherapy efficiency. Strikingly, ibrutinib treatment enhances chemotherapeutic effectiveness, by targeting pericytes, improving blood-brain barrier permeability, and prolonging survival. This study identifies glioblastoma-derived pericyte as a novel target in the brain tumor microenvironment during carcinogenesis. Here, we summarize and evaluate recent advances in the understanding of pericyte's role in the glioblastoma microenvironment.

SUBMITTER: Guerra DAP 

PROVIDER: S-EPMC6238207 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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Targeting glioblastoma-derived pericytes improves chemotherapeutic outcome.

Guerra Daniel A P DAP   Paiva Ana E AE   Sena Isadora F G IFG   Azevedo Patrick O PO   Silva Walison N WN   Mintz Akiva A   Birbrair Alexander A  

Angiogenesis 20180514 4


Glioblastoma is the most common malignant brain cancer in adults, with poor prognosis. The blood-brain barrier limits the arrival of several promising anti-glioblastoma drugs, and restricts the design of efficient therapies. Recently, by using state-of-the-art technologies, including thymidine kinase targeting system in combination with glioblastoma xenograft mouse models, it was revealed that targeting glioblastoma-derived pericytes improves chemotherapy efficiency. Strikingly, ibrutinib treatm  ...[more]

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