Evidence map›Paper›PMID 29562708›Full record

ArticleInternational journal of molecular sciences2018

HER2-Targeted Multifunctional Silica Nanoparticles Specifically Enhance the Radiosensitivity of HER2-Overexpressing Breast Cancer Cells.

Haruka Yamaguchi, Kazuhide Hayama, Ichiro Sasagawa, Yasuo Okada, Tomoyuki Kawase, Norio Tsubokawa, Makoto Tsuchimochi

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. Article
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  12. Mesoporous Silica Nanoparticles for Targeting Subcellular Organelles.International journal of molecular sciences · 2020
    Review
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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

7 authors.

Haruka YamaguchiDepartment of Life Science Dentistry, The Nippon Dental University, 1-8 Hamauracho, Chuoku, Niigata 951-8580, Japan. harukay@ngt.ndu.ac.jp.ORCID 0000-0002-1393-5855
Kazuhide HayamaDepartment of Oral and Maxillofacial Radiology, The Nippon Dental University School of Life Dentistry at Niigata, Niigata 951-8580, Japan. hayama@ngt.ndu.ac.jp.
Ichiro SasagawaAdvanced Research Center, The Nippon Dental University School of Life Dentistry at Niigata, Niigata 951-8580, Japan. ichsasgw@ngt.ndu.ac.jp.ORCID 0000-0002-2160-8088
Yasuo OkadaDepartment of Pathology, The Nippon Dental University School of Life Dentistry at Niigata, Niigata 951-8580, Japan. yokada@ngt.ndu.ac.jp.
Tomoyuki KawaseDivision of Oral Bioengineering, Department of Tissue Regeneration and Reconstitution, Niigata University Graduate School of Medical and Dental Sciences, Niigata 951-8541, Japan. kawase@dent.niigata-u.ac.jp.ORCID 0000-0003-4160-396X
Norio TsubokawaFaculty of Engineering, Niigata University, Niigata 950-2181, Japan. ntsuboka@eng.niigata-u.ac.jp.
Makoto TsuchimochiEmeritus Professor, The Nippon Dental University, Tokyo 102-8159, Japan. tsuchimochi@ngt.ndu.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated the effects of targeted functionalized silica nanoparticles on the radiosensitivity of cancer cells. Better control of the local concentration of silica nanoparticles may facilitate their use as an adjuvant in conjunction with ionizing radiation to target cancer cells while preventing damage to normal cells. Hyperbranched polyamidoamine (PAMAM) was grafted onto the surface of amorphous silica nanoparticles to functionalize them. The PAMAM-coated silica nanoparticles (PCSNs) were then conjugated with fluorescent dyes. Anti-HER2 antibodies were covalently attached to the labeled PCSNs. The HER2-overexpressing SK-BR3 breast cancer cell line was incubated in medium containing the PCSN probes. After incubation; the cells were exposed to X-ray radiation. Cells were counted in all samples using cell proliferation assays; and apoptotic cells were detected. The cell survival results showed that the combination of the targeted PCSN probes and radiation reduced the survival rate of SK-BR3 cells to a greater extent than when either PCSN probes, PCSNs or radiation were applied individually. The results also showed an increase in apoptosis in the SK-BR3 cells that internalized the PCSN probes and were then irradiated. Based on these data, PCSN probes act as specific radiosensitizing agents for HER2-overexpressing cells.

Indexed as

Radiation ToleranceBreast NeoplasmsCell Line, TumorCell NucleusCell ProliferationCell SurvivalErb-b2 Receptor Tyrosine KinasesFemaleFluorescenceHumansLysosomesNanoparticlesParticle SizePolyaminesSilicon DioxideErb-b2 Receptor Tyrosine KinasesPoly(amidoamine)PolyaminesSilicon DioxideHER2radiosensitizersilica nanoparticleSK-BR3

Identifiers

PMID29562708
PMCPMC5877769

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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.