Evidence map›Paper›PMID 26030072›Full record

ArticlePloS one2015

Defined nanoscale chemistry influences delivery of peptido-toxins for cancer therapy.

Santosh K Misra, Mao Ye, Sumin Kim, Dipanjan Pan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.5field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Intrinsic apoptotic effect of Anatolian honeybee (Turkish journal of biology = Turk biyoloji dergisi · 2025
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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.

Santosh K MisraDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Beckman Institute of Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Department of Materials Science and Engineering University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Carle Foundation Hospital, Urbana, IL, 61801, United States of America.
Mao YeDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Beckman Institute of Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Department of Materials Science and Engineering University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Carle Foundation Hospital, Urbana, IL, 61801, United States of America.
Sumin KimDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Beckman Institute of Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Department of Materials Science and Engineering University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Carle Foundation Hospital, Urbana, IL, 61801, United States of America.
Dipanjan PanDepartment of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Beckman Institute of Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Department of Materials Science and Engineering University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States of America; Carle Foundation Hospital, Urbana, IL, 61801, United States of America.
Carle Foundation Hospital · USUniversity of Illinois Urbana-Champaign · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present an in-silico-to-in-vitro approach to develop well-defined, self-assembled, rigid-cored polymeric (Polybee) nano-architecture for controlled delivery of a key component of bee venom, melittin. A competitive formulation with lipid-encapsulated (Lipobee) rigid cored micelle is also synthesized. In a series of sequential experiments, we show how nanoscale chemistry influences the delivery of venom toxins for cancer regression and help evade systemic disintegrity and cellular noxiousness. A relatively weaker association of melittin in the case of lipid-based nanoparticles is compared to the polymeric particles revealed by energy minimization and docking studies, which are supported by biophysical studies. For the first time, the authors' experiment results indicate that melittin can play a significant role in DNA association-dissociation processes, which may be a plausible route for their anticancer activity.

Indexed as

Antineoplastic AgentsMelittenMolecular Docking SimulationNanoparticlesPolymersProtein Structure, SecondaryAntineoplastic AgentsMelittenPolymers

Identifiers

PMID26030072
PMCPMC4452514
OpenAlexW2199014725

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.