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Molecularly targeted therapies for glioma
Ryuya Yamanaka1, Hideyuki Saya
1Research Center of Innovative Cancer Therapy, Kurume University School of Medicine, Fukuoka, Japan. ryaman@med.kurume-u.ac.jp
Abstract:
Over the past decade, molecularly targeted therapies have been added to cytotoxic and antiendocrine drugs in the treatment of cancer, with the aim of targeting the molecular pathways that underlie the carcinogenic process and maintain the cancer phenotype. Success with some of these agents has suggested that identification and validation of drug targets is the starting point for the development of active, safe, and effective drugs. The main molecular targets used to develop anticancer drugs are cell surface receptors, signal transduction pathways, gene transcription targets, ubiquitin-proteasome/heat shock proteins, and tumor microenvironment components. Here, we review the development of the main molecularly targeted noncytotoxic agents studied in glioma, highlighting lessons derived from the development of these novel drugs and proposing new horizons for the clinical development of molecularly targeted therapies.
Insights
Molecularly targeted therapies offer a new approach to cancer treatment by targeting specific molecular pathways. This review highlights advancements in targeted therapies for glioma, focusing on future clinical development.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Molecularly targeted therapies are increasingly used alongside traditional cancer treatments like cytotoxic and antiendocrine drugs.
- These therapies aim to disrupt specific molecular pathways crucial for cancer development and maintenance.
- Identifying and validating drug targets is essential for developing effective and safe anticancer agents.
Purpose of the Study:
- To review the development of molecularly targeted noncytotoxic agents for glioma treatment.
- To highlight key lessons learned from the clinical development of these novel drugs.
- To propose future directions for molecularly targeted therapy in glioma.
Main Methods:
- Review of existing literature on molecularly targeted therapies in glioma.
- Analysis of drug development strategies targeting key molecular pathways.
- Examination of common molecular targets including cell surface receptors, signal transduction pathways, and tumor microenvironment components.
Main Results:
- Several molecularly targeted agents have been studied in glioma, showing promise.
- The development process has provided valuable insights into target identification and validation.
- Understanding molecular pathways is critical for therapeutic success.
Conclusions:
- Molecularly targeted therapies represent a significant advancement in cancer treatment, particularly for glioma.
- Continued research into novel drug targets and therapeutic strategies is crucial.
- Future clinical development should focus on refining these targeted approaches for improved patient outcomes.
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