Oct 23, 2018

Convective forces increase CXCR4-dependent glioblastoma cell invasion in GL261 murine model

BioRxiv : the Preprint Server for Biology
R Chase CornelisonJennifer M Munson

Abstract

Glioblastoma is the most common and malignant form of brain cancer. Its invasive nature limits treatment efficacy and promotes inevitable recurrence. Previous in vitro studies showed that interstitial fluid flow, a factor characteristically increased in cancer, increases glioma cell invasion through CXCR4-CXCL12 signaling. It is currently unknown if these effects translate in vivo. We used the therapeutic technique of convection enhanced delivery (CED) to test if convective flow alters glioma invasion in a syngeneic GL261 mouse model of glioblastoma. The GL261 cell line was flow responsive in vitro dependent upon CXCR4 and CXCL12. Additionally, transplanting GL261 intracranially increased the populations of CXCR4+ and double positive cells versus 3D culture. We showed that inducing convective flow within implanted tumors indeed increased invasion over untreated controls, and administering the CXCR4 antagonist AMD3100 (5 mg/kg) effectively eliminated this response. These data confirm that glioma invasion is stimulated by convective flow in vivo and depends on CXCR4 signaling. We also showed that expression of CXCR4 and CXCL12 is increased in patients having received standard therapy when CED might be elected. Hence, targeting fl...Continue Reading

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Mentioned in this Paper

Standard of Care
In Vivo
Stromal Cell-Derived Factor 1
Convection Enhanced Delivery of Intracerebral Catheter(S)
Drug Delivery Systems
Cxcr4
CXCR4 gene
CXCL12 gene
Murine
Antagonist Muscle Action

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