Evidence map›Paper›PMID 28333127›Full record

ArticleScientific reports2017

Selective intracellular vaporisation of antibody-conjugated phase-change nano-droplets in vitro.

A Ishijima, K Minamihata, S Yamaguchi, S Yamahira, R Ichikawa, E Kobayashi, M Iijima, Y Shibasaki, T Azuma, T Nagamune and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 31 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

11 authors at 2 institutions in 1 country.

A IshijimaDepartment of Precision Engineering, School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
K MinamihataDepartment of Applied Chemistry, Kyushu University, Fukuoka 819-0395, Japan.
S YamaguchiResearch Center for Advanced Science and Technology, The University of Tokyo, Tokyo 153-8904, Japan.
S YamahiraDepartment of Chemistry &Biotechnology, School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
R IchikawaDepartment of Precision Engineering, School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
E KobayashiDepartment of Precision Engineering, School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
M IijimaResearch Center for Advanced Science and Technology, The University of Tokyo, Tokyo 153-8904, Japan.
Y ShibasakiResearch Center for Advanced Science and Technology, The University of Tokyo, Tokyo 153-8904, Japan.
T AzumaCenter for Disease Biology and Integrative Medicine, The University of Tokyo, Tokyo 113-8656, Japan.
T NagamuneDepartment of Chemistry &Biotechnology, School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
I SakumaDepartment of Precision Engineering, School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
The University of Tokyo · JPKyushu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While chemotherapy is a major mode of cancer therapeutics, its efficacy is limited by systemic toxicities and drug resistance. Recent advances in nanomedicine provide the opportunity to reduce systemic toxicities. However, drug resistance remains a major challenge in cancer treatment research. Here we developed a nanomedicine composed of a phase-change nano-droplet (PCND) and an anti-cancer antibody (9E5), proposing the concept of ultrasound cancer therapy with intracellular vaporisation. PCND is a liquid perfluorocarbon nanoparticle with a liquid-gas phase that is transformable upon exposure to ultrasound. 9E5 is a monoclonal antibody targeting epiregulin (EREG). We found that 9E5-conjugated PCNDs are selectively internalised into targeted cancer cells and kill the cells dynamically by ultrasound-induced intracellular vaporisation. In vitro experiments show that 9E5-conjugated PCND targets 97.8% of high-EREG-expressing cancer cells and kills 57% of those targeted upon exposure to ultrasound. Furthermore, direct observation of the intracellular vaporisation process revealed the significant morphological alterations of cells and the release of intracellular contents.

Indexed as

AnimalsAntibodies, MonoclonalAnticarcinogenic AgentsCell Line, TumorEpiregulinHumansIn Vitro TechniquesMice, Inbred BALB CNanoconjugatesNanomedicineNeoplasmsUltrasonic TherapyAntibodies, MonoclonalAnticarcinogenic AgentsEpiregulinEREG protein, humanNanoconjugates

Identifiers

PMID28333127
PMCPMC5363066
OpenAlexW2598971651

What OpenQuestion holds

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LicenceCC BY
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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.