Evidence map›Paper›PMID 28887524›Full record

ArticleScientific reports2017

Selective uptake of epidermal growth factor-conjugated gold nanoparticle (EGF-GNP) facilitates non-thermal plasma (NTP)-mediated cell death.

Wanil Kim, Kyung-Yoon Na, Kyung-Ha Lee, Hyun Wook Lee, Jae Koo Lee, Kyong-Tai Kim

Abstract 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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 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.

Wanil KimDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Kyung-Yoon NaDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Kyung-Ha LeeDivision of Biotechnology and Convergence, Daegu Haany University, Gyeongsan, 38610, Republic of Korea.
Hyun Wook LeeDepartment of Electronic and Electrical Engineering, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.ORCID 0000-0002-1472-8647
Jae Koo LeeDepartment of Electronic and Electrical Engineering, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
Kyong-Tai KimDepartment of Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea. ktk@postech.ac.kr.ORCID 0000-0001-7292-2627

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-thermal atmospheric pressure plasma (NTP) has been shown to induce cell death in various mammalian cancer cells. Accumulated evidence also shows that NTP could be clinically used in cancer therapy. However, the current NTP-based applications lack target specificity. Here, a novel method in NTP-mediated cancer therapeutics was described with enhanced target specificity by treating EGF (epidermal growth factor)-conjugated GNP (gold nanoparticle). The treatment with EGF-conjugated GNP complex, followed by NTP irradiation showed selective apoptosis of cells having receptor-mediated endocytosis. NTP triggered γ-H2AX elevation which is a typical response elicited by DNA damage. These results suggest that EGF-conjugated GNP functions as an important adjuvant which gives target specificity in applications of conventional plasma therapy.

Indexed as

ApoptosisAntineoplastic AgentsDNA DamageEpidermal Growth FactorGoldHeLa CellsHT29 CellsHumansMetal NanoparticlesNanoconjugatesPlasma GasesAntineoplastic AgentsEpidermal Growth FactorGoldNanoconjugatesPlasma Gases

Identifiers

PMID28887524
PMCPMC5591291

What OpenQuestion holds

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Registered trials

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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.