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Modulation of blood-tumor barrier transcriptional programs improves intra-tumoral drug delivery and potentiates chemotherapy in GBM.

Authors :
Jimenez-Macias JL
Vaughn-Beaucaire P
Bharati A
Xu Z
Forrest M
Hong J
Sun M
Schmidt A
Clark J
Hawkins W
Mercado N
Real J
Huntington K
Zdioruk M
Nowicki MO
Cho CF
Wu B
Li W
Logan T
Manz KE
Pennell KD
Fedeles BI
Brodsky AS
Lawler SE
Source :
BioRxiv : the preprint server for biology [bioRxiv] 2024 Aug 28. Date of Electronic Publication: 2024 Aug 28.
Publication Year :
2024

Abstract

Glioblastoma (GBM) is the most common malignant primary brain tumor. GBM has an extremely poor prognosis and new treatments are badly needed. Efficient drug delivery to GBM is a major obstacle as the blood-brain barrier (BBB) prevents passage of the majority of cancer drugs into the brain. It is also recognized that the blood-brain tumor barrier (BTB) in the growing tumor represents a challenge. The BTB is heterogeneous and poorly characterized, but similar to the BBB it can prevent therapeutics from reaching effective intra-tumoral doses, dramatically hindering their potential. Here, we identified a 12-gene signature associated with the BTB, with functions related to vasculature development, morphogenesis and cell migration. We identified CDH5 as a core molecule in this set and confirmed its over-expression in GBM vasculature using spatial transcriptomics of GBM patient specimens. We found that the indirubin-derivative, 6-bromoindirubin acetoxime (BIA), could downregulate CDH5 and other BTB signature genes, causing endothelial barrier disruption in endothelial monolayers and BBB 3D spheroids in vitro . Treatment of tumor-bearing mice with BIA enabled increased intra-tumoral accumulation of the BBB non-penetrant chemotherapeutic drug cisplatin and potentiated cisplatin-mediated DNA damage by targeting DNA repair pathways. Finally, using an injectable BIA nanoparticle formulation, PPRX-1701, we significantly improved the efficacy of cisplatin in patient-derived GBM xenograms and prolonged their survival. Overall, our work reveals potential targets at the BTB for improved chemotherapy delivery and the bifunctional properties of BIA as a BTB modulator and potentiator of chemotherapy, supporting its further development.<br />Competing Interests: Competing interests B.W. has ownership interests in both Cytodigm, Inc. and Phosphorex, LLC. B.W. is also a board member, officer and employee of Phosphorex, LLC. In addition, B.W. has patents US10,039,829, US10,675,350, WO2013/192493, WO2018/025075. W.L. was an employee of Phosphorex, Inc. and a current employee of Prime Medicine. T.L. was an employee of Phosphorex, Inc. and a current employee of Phosphorex, LLC.

Details

Language :
English
ISSN :
2692-8205
Database :
MEDLINE
Journal :
BioRxiv : the preprint server for biology
Publication Type :
Academic Journal
Accession number :
39253453
Full Text :
https://doi.org/10.1101/2024.08.26.609797