Evidence map›Paper›PMID 29378114›Full record

ReviewACS nano2018

Nanoparticles for Immune Cytokine TRAIL-Based Cancer Therapy.

Pedro P G Guimarães, Stephanie Gaglione, Tomasz Sewastianik, Ruben D Carrasco, Robert Langer, Michael J Mitchell

Abstract readReview
In one paragraph

Review in ACS nano, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Pedro P G GuimarãesDepartment of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, MIT , Cambridge, Massachusetts 02139, United States.
Stephanie GaglioneDepartment of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, MIT , Cambridge, Massachusetts 02139, United States.
Tomasz SewastianikDepartment of Oncologic Pathology, Dana-Farber Cancer Institute, Harvard Medical School , Boston, Massachusetts 02215, United States.
Ruben D CarrascoDepartment of Oncologic Pathology, Dana-Farber Cancer Institute, Harvard Medical School , Boston, Massachusetts 02215, United States.
Robert LangerDepartment of Chemical Engineering, David H. Koch Institute for Integrative Cancer Research, MIT , Cambridge, Massachusetts 02139, United States.ORCID 0000-0003-4255-0492
Michael J MitchellDepartment of Bioengineering, University of Pennsylvania , Philadelphia, Pennsylvania 19104, United States.ORCID 0000-0002-3628-2244

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MATTHEW G. VANDER HEIDEN · 1985 to 2026
$93.9M
Polymeric Nanoparticles for siRNA Delivery to Bone Marrow Endothelium to Disrupt Tumor Cell Adhesion and Bone Metastasis Formation In VivoF32CA200351 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MITCHELL, MICHAEL J · 2015 to 2017
$164k
NCI NIH HHS F32 CA200351NCI NIH HHS P30 CA014051
6 · The paper itself

Abstract

The immune cytokine tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) has received significant attention as a cancer therapeutic due to its ability to selectively trigger cancer cell apoptosis without causing toxicity in vivo. While TRAIL has demonstrated significant promise in preclinical studies in mice as a cancer therapeutic, challenges including poor circulation half-life, inefficient delivery to target sites, and TRAIL resistance have hindered clinical translation. Recent advances in drug delivery, materials science, and nanotechnology are now being exploited to develop next-generation nanoparticle platforms to overcome barriers to TRAIL therapeutic delivery. Here, we review the design and implementation of nanoparticles to enhance TRAIL-based cancer therapy. The platforms we discuss are diverse in their approaches to the delivery problem and provide valuable insight into guiding the design of future nanoparticle-based TRAIL cancer therapeutics to potentially enable future translation into the clinic.

Indexed as

AnimalsApoptosisCell ProliferationDrug Delivery SystemsHumansNanoparticlesNeoplasmsParticle SizeSurface PropertiesTNF-Related Apoptosis-Inducing LigandTNF-Related Apoptosis-Inducing Ligandbiological barriersbiomaterialscancer therapydrug deliverygene therapyimmunotherapymetastasisnanotechnologyoncologytumor targeting

Identifiers

PMID29378114
PMCPMC5834400

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.