Evidence map›Paper›PMID 27274243›Full record

ArticleInternational journal of nanomedicine2016

In vitro and in vivo targeting imaging of pancreatic cancer using a Fe3O4@SiO2 nanoprobe modified with anti-mesothelin antibody.

Fang Liu, Wenjun Le, Tianxiao Mei, Tiegong Wang, Luguang Chen, Yi Lei, Shaobin Cui, Bingdi Chen, Zheng Cui, Chengwei Shao

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

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  5. Time- and Spectrally-Resolved Photoluminescence Study of Alloyed CdInternational journal of molecular sciences · 2022
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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

10 authors at 2 institutions in 1 country.

Fang LiuRadiology Department of Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Wenjun LeShanghai East Hospital, The Institute for Biomedical Engineering & Nano Science, Tongji University School of Medicine, Shanghai, People's Republic of China.
Tianxiao MeiShanghai East Hospital, The Institute for Biomedical Engineering & Nano Science, Tongji University School of Medicine, Shanghai, People's Republic of China.
Tiegong WangRadiology Department of Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Luguang ChenRadiology Department of Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Yi LeiRadiology Department of Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Shaobin CuiShanghai East Hospital, The Institute for Biomedical Engineering & Nano Science, Tongji University School of Medicine, Shanghai, People's Republic of China.
Bingdi ChenShanghai East Hospital, The Institute for Biomedical Engineering & Nano Science, Tongji University School of Medicine, Shanghai, People's Republic of China.
Zheng CuiShanghai East Hospital, The Institute for Biomedical Engineering & Nano Science, Tongji University School of Medicine, Shanghai, People's Republic of China; Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Chengwei ShaoRadiology Department of Changhai Hospital, Second Military Medical University, Shanghai, People's Republic of China.
Second Military Medical University · CNShanghai East Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is a highly malignant disease with a 5-year survival rate <5% mainly due to lack of early diagnosis and effective therapy. In an effort to improve the early diagnostic rate of pancreatic cancer, a nanoprobe Fe3O4@SiO2 modified with anti-mesothelin antibody (A-MFS) was prepared to target cells and tumor tissues highly expressing mesothelin in vitro (human pancreatic cancer cell line SW1990) and in vivo (subcutaneously transplanted tumors) studies. The A-MFS probe was successfully prepared and was spherical and uniform with a hydrodynamic diameter between 110 and 130 nm. Cell Counting Kit-8 testing indicated that A-MFS was nontoxic in vitro and in vivo studies. The in vitro study showed that the A-MFS probe specifically targeted SW1990 cells with high mesothelin expression. The in vivo study was conducted in Siemens 3.0 T magnetic resonance imaging. The average T2-weighted signal values of the xenografts were 966.533±31.56 before injecting A-MFS and 691.133±56.84 before injecting saline solution. After injection of 0.1 mL A-MFS via nude mouse caudal vein for 2.5 hours, the average T2-weighted signal of the xenograft decreased by 342.533±42.6. The signal value decreased by -61.233±33.9 and -58.7±19.4 after injection of the saline and Fe3O4@SiO2. The decrease of tumor signal by A-MFS was much more significant than that by saline and Fe3O4@SiO2 (P<0.05). The results demonstrated the high stability and nontoxicity of A-MFS, which effectively targeted pancreatic cancer in vitro and in vivo. A-MFS is a promising agent for diagnosis of pancreatic cancer.

Indexed as

Drug Delivery SystemsMagnetic Resonance ImagingAnimalsAntibodiesCell DeathCell Line, TumorCell SurvivalDextransFlow CytometryGPI-Linked ProteinsHumansIronMagnetite NanoparticlesMaleMesothelinMice, Inbred BALB CAntibodiesDextransferumoxidesGPI-Linked ProteinsIronMagnetite NanoparticlesMesothelinMsln protein, mouseSilicon DioxideFe3O4@SiO2mesothelinnanoprobepancreatic cancertargeted imaging

Identifiers

PMID27274243
PMCPMC4876944
OpenAlexW2396193894

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.