Facilitating tailored therapeutic strategies for glioblastoma through an orthotopic patient-derived xenograft platform.

Histol Histopathol

Institute for Refractory Cancer Research, Samsung Medical Center, Department of Health Sciences and Technology, SAIHST, Sungkyunkwan University and Departments of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea

Published: March 2016

AI Article Synopsis

  • Despite extensive research and clinical trials, glioblastoma (GBM) patients still face poor outcomes due to complex tumor variations and the presence of self-renewing GBM stem cells (GSCs).
  • Advances in multi-omics technology are paving the way for personalized therapy approaches, focusing on targeted treatments rather than traditional non-selective methods.
  • The article emphasizes the importance of using GBM orthotopic patient-derived xenografts (PDXs) as effective models for validating drug targets, developing diagnostics, and ultimately improving treatment outcomes for GBM patients.

Article Abstract

Despite years of research into its pathobiology and continuing clinical trials for novel therapies, the prognosis for patients with glioblastoma (GBM) remains dismal. An important obstacle against treatment efficacy may be a high degree of intra- and inter-tumoral heterogeneity within GBMs, which may be caused by the presence of self-renewing GBM stem cells (GSCs). Recent advances in multi-omics technology introduce new possibilities for applying personalized strategies to GBM therapy. As drug discovery is accelerating with the transition from non-selective, cytotoxic therapy to a precision, targeted approach, the appropriate in vivo platform for GBM is critical for validating drug targets and prioritizing candidates for clinical studies, for co-development of companion diagnostics and, ultimately, for drug approval. Here we will describe GBM orthotopic patient-derived xenografts (PDXs) as more useful, clinically relevant resources for individually tailored strategies for GBM.

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Source
http://dx.doi.org/10.14670/HH-11-695DOI Listing

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