Evidence map›Paper›PMID 23444913›Full record

ArticleBiomacromolecules2013

Synergistic antitumor activity from two-stage delivery of targeted toxins and endosome-disrupting nanoparticles.

Xingfang Su, Nicole Yang, K Dane Wittrup, Darrell J Irvine

Open access · greenAbstract read
In one paragraph

Article in Biomacromolecules, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.2field-weighted citation impact, top 43% of its field
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

7 citing papers in PubMed, 1 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Xingfang SuDepartment of Material Science and Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, USA.
Nicole Yang
K Dane Wittrup
Darrell J Irvine
Massachusetts Institute of Technology · USRagon Institute of MGH, MIT and Harvard · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MATTHEW G. VANDER HEIDEN · 1985 to 2026
$93.9M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA014051
6 · The paper itself

Abstract

Plant-derived Type I toxins are candidate anticancer therapeutics requiring cytosolic delivery into tumor cells. We tested a concept for two-stage delivery, whereby tumor cells precoated with an antibody-targeted gelonin toxin were killed by exposure to endosome-disrupting polymer nanoparticles. Co-internalization of particles and tumor cell-bound gelonin led to cytosolic delivery and >50-fold enhancement of toxin efficacy. This approach allows the extreme potency of gelonin to be focused on tumors with significantly reduced potential for off-target toxicity.

Indexed as

Drug CarriersAnimalsAntibodiesAntineoplastic AgentsAntineoplastic Agents, PhytogenicCell Line, TumorDextransEndosomesHumansMiceNanoparticlesNeoplasmsPhalloidineRibosome Inactivating Proteins, Type 1AntibodiesAntineoplastic AgentsAntineoplastic Agents, PhytogenicDextransDrug CarriersGEL protein, Gelonium multiflorumPhalloidineRibosome Inactivating Proteins, Type 1

Identifiers

PMID23444913
PMCPMC3646422
OpenAlexW1590919939

What OpenQuestion holds

Textmetadata
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.