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Open AccessJournal ArticleDOI

TRAIL on trial: preclinical advances in cancer therapy.

Daniel W. Stuckey, +1 more
- 01 Nov 2013 - 
- Vol. 19, Iss: 11, pp 685-694
TLDR
How TRAIL has been functionalized to diversify its traditional tumor-killing role and novel strategies to facilitate its effective deployment in preclinical cancer models are discussed.
About
This article is published in Trends in Molecular Medicine.The article was published on 2013-11-01 and is currently open access. It has received 241 citations till now. The article focuses on the topics: Targeted therapy.

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Citations
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Stem cell-based therapies for cancer treatment: separating hope from hype

TL;DR: This perspective considers the current status of stem cell-based treatments for cancer and provides a rationale for translating the most promising preclinical studies into the clinic.
Journal ArticleDOI

Cancer stem cell targeted therapy: progress amid controversies

TL;DR: The current status and progresses of cancer stem cells theory is illustrated and via providing a panoramic view of cancer therapy, the recent controversies regarding the feasibility of cancerstem cells targeted anti-cancer therapy are addressed.
Journal ArticleDOI

Cancer-Targeting Nanoparticles for Combinatorial Nucleic Acid Delivery

TL;DR: Classes of nucleic acids, hurdles that must be overcome for effective intracellular delivery, types of nonviral nanomaterials used as delivery vehicles, and the different strategies that can be employed to target nucleic acid delivery specifically to tumor cells are discussed.
Journal ArticleDOI

Stem cells in cancer therapy: opportunities and challenges.

TL;DR: This review focuses on recent progress toward stem cell-based cancer treatments, and summarizes treatment advantages, opportunities, and shortcomings, potentially helping to refine future trials and facilitate the translation from experimental to clinical studies.
Journal ArticleDOI

Nanoparticles for Immune Cytokine TRAIL-Based Cancer Therapy

TL;DR: The design and implementation of nanoparticles to enhance TRAIL-based cancer therapy are reviewed and valuable insight is provided into guiding the design of future nanoparticle-based TRAIL cancer therapeutics to potentially enable future translation into the clinic.
References
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Global cancer statistics

TL;DR: A substantial proportion of the worldwide burden of cancer could be prevented through the application of existing cancer control knowledge and by implementing programs for tobacco control, vaccination, and early detection and treatment, as well as public health campaigns promoting physical activity and a healthier dietary intake.
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Hallmarks of cancer: the next generation.

TL;DR: Recognition of the widespread applicability of these concepts will increasingly affect the development of new means to treat human cancer.
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Identification and characterization of a new member of the TNF family that induces apoptosis

TL;DR: A novel tumor necrosis factor (TNF) family member has been cloned and characterized, and the TRAIL gene is located on chromosome 3 at position 3q26, which is not close to any other known TNF ligand family members.
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Tumoricidal activity of tumor necrosis factor-related apoptosis-inducing ligand in vivo

TL;DR: Recurrent treatments with LZ–huTRAIL actively suppressed growth of the TRAIL–sensitive human mammary adenocarcinoma cell line MDA–231 in CB.17 (SCID) mice, and histologic examination of tumors from SCID mice treated with Lz–hu TRAIL demonstrated clear areas of apoptotic necrosis within 9–12 hours of injection.
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Apoptosis: a link between cancer genetics and chemotherapy.

TL;DR: Understanding the molecular events that contribute to drug-induced apoptosis, and how tumors evade apoptotic death, provides a paradigm to explain the relationship between cancer genetics and treatment sensitivity and should enable a more rational approach to anticancer drug design and therapy.
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