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Targeting glioblastoma-derived pericytes improves chemotherapeutic outcome

期刊

ANGIOGENESIS
卷 21, 期 4, 页码 667-675

出版社

SPRINGER
DOI: 10.1007/s10456-018-9621-x

关键词

Pericytes; Glioblastoma; Blood-brain barrier; Chemotherapy

资金

  1. Pro-reitoria de Pesquisa/Universidade Federal de Minas Gerais (PRPq/UFMG) [Edital 05/2016]
  2. FAPEMIG [Rede Mineira de Engenharia de Tecidos e Terapia Celular (REMETTEC)] [RED-00570-16]
  3. National Institute of Health [1R01CA179072-01A1]
  4. American Cancer Society Mentored Research Scholar Grant [124443-MRSG-13-121-01-CDD]
  5. FAPEMIG [Rede De Pesquisa Em Doencas Infecciosas Humanas E Animais Do Estado De Minas Gerais] [RED-00313-16]
  6. Instituto Serrapilheira/Serra [1708-15285]

向作者/读者索取更多资源

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.

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