PO.TB05.02 · 肿瘤生物学

Site-specific tumor modeling: DIPG and meningioma in mice

海报缩略图:Site-specific tumor modeling: DIPG and meningioma in mice
编号 6184 展板 20 时间 4/21 02:00–05:00 区域 Section 30 主讲 Melissa Tran, PhD
分会场 Pediatric Cancer Models
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作者与单位

Melissa Tran1, Cheryl Davis2, Ben Hoerner1, Victoria Caruso1, Helen Ketteringham3, Corrine Silvio4, Shannan Paul3, Chris Holding3, Aliccia Koznecki3, Dawn Lusk4, Shorena Nadaraia-Hoke4, Delaney McCormick1, Jocelyn Saurbaugh1

1Reaction Biology Corp, Malvern, PA,2Reaction Biology Europe GmbH, Freiburg im Breisgau, Germany,3Reaction Biology Corp, Hershey, PA,4Reaction Biology Corp, Hummelstown, PA

摘要 Abstract

Diffuse intrinsic pontine glioma (DIPG) and meningioma are central nervous system tumors where anatomical location critically influences disease behavior and therapeutic response. To investigate this impact, we have developed and compared preclinical models using SF8628-GFP⁺/Luc⁺ (DIPG) and Ben-Men-1-Luc (meningioma) across three inoculation sites: (1) clinically relevant locations (pons for DIPG; skull base for meningioma), (2) general intracranial sites, and (3) subcutaneous sites. Tumor progression was monitored longitudinally using bioluminescence imaging and confirmed by histopathology. This study sought to determine how site-specific microenvironments affect growth kinetics, infiltration patterns, and imaging characteristics. Understanding these differences is essential for drug development, as orthotopic models better replicate blood-brain barrier constraints, tumor vascularization, and local tissue interactions that influence therapeutic delivery and efficacy.
利益披露 Disclosure
M. Tran, None.. C. Davis, None.. D. McCormick, None.. J. Saurbaugh, None.

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