Evidence map›Paper›PMID 26719671›Full record

ArticleDrug design, development and therapy2015

The study on the preparation and characterization of gene-loaded immunomagnetic albumin nanospheres and their anti-cell proliferative effect combined with magnetic fluid hyperthermia on GLC-82 cells.

Hao Zhang, Xinxin Hou, Mei Lin, Ling Wang, Hongbo Li, Chenyan Yuan, Chen Liang, Jia Zhang, Dongsheng Zhang

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. The therapeutic effect of PEI-FeFrontiers in oncology · 2023
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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

9 authors at 1 institution in 1 country.

Hao ZhangMedical School of Southeast University, Nanjing, Jiangsu, People's Republic of China.
Xinxin HouMedical School of Henan Polytechnic University, Jiaozuo, Henan, People's Republic of China.
Mei LinTaizhou People's Hospital Affiliated to Nantong University, Taizhou, Jiangsu, People's Republic of China.
Ling WangMedical School of Southeast University, Nanjing, Jiangsu, People's Republic of China.
Hongbo LiDepartment of Ultrasound in Medicine, The First Affiliated Hospital (Jiangsu Province Hospital of TCM), Nanjing University of Chinese Medicine, Nanjing, Jiangsu, People's Republic of China.
Chenyan YuanMedical School of Southeast University, Nanjing, Jiangsu, People's Republic of China.
Chen LiangMedical School of Southeast University, Nanjing, Jiangsu, People's Republic of China.
Jia ZhangJiangsu Cancer Hospital, Nanjing, Jiangsu, People's Republic of China.
Dongsheng ZhangMedical School of Southeast University, Nanjing, Jiangsu, People's Republic of China ; Jiangsu Key Laboratory For Biomaterials and Devices, Nanjing, Jiangsu, People's Republic of China.
Jiangsu Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As one of the most common malignant tumors, the clinical and socio-economic consequences of lung cancer are significant. Currently, surgery is the main treatment strategy for this disease, but the survival rates of lung cancer patients are not ideal due to the high recurrence rate of the disease. Therefore, many researchers are exploring new specific therapeutic methods that are highly curative and minimally cytotoxic to healthy tissues. To this end, albumin nanospheres simultaneously were loaded with super-paramagnetic iron oxide nanoparticles (as gene vector and anticancer gene), and plasmid pDONR223-IFNG, and modified with anti-EGFR monoclonal antibody cetuximab as therapy. Targeting agents, namely gene-loaded immunomagnetic albumin nanospheres (cetuximab [C225]-IFNG-IMANS), were prepared for targeted lung carcinoma cells (GLC-82 cell lines). Transmission electron microscopy images showed that the C225-IFNG-IMANS were successfully prepared, and the ability of the nanospheres to target GLC-82 cells in vitro was confirmed by Prussian blue staining, immunofluorescence experiments, and magnetic resonance imaging. Transfection photographs and agarose gel electrophoresis proved that pDONR223-IFNG could be encased in the albumin nanospheres. A Cell Counting Kit-8 assay showed that the combination therapy group had significantly more therapeutic effects on GLC-82 cells than other therapy groups. A flow cytometry assay showed that the apoptotic index of the combined treatment group was 67.68%, whereas the indices of the C225 group, gene therapy group, and magnetic fluid hyperthermia group were 12.2%, 16.34%, and 20.04% respectively. Therefore, the combination of thermal treatment, molecular targeted treatment, and gene treatment synergistically targets GLC-82 cells, and the use of C225-IFNG-IMANS as a gene or drug carrier offers a novel and promising approach for the treatment of lung cancer.

Indexed as

Gene Transfer TechniquesHypothermia, InducedAlbuminsAntineoplastic AgentsApoptosisCell Line, TumorCell ProliferationCetuximabDrug CarriersErbB ReceptorsGenetic TherapyHumansIminesInterferon-gammaLung NeoplasmsMagnetic Resonance ImagingAlbuminsAntineoplastic AgentsCetuximabDrug CarriersEGFR protein, humanErbB ReceptorsIminesInterferon-gammaMagnetite Nanoparticlespoly(ethylene imine)PolyethylenesProtein Kinase Inhibitorsmagnetic nanoparticlesnano-drugtargeting gene therapy

Identifiers

PMID26719671
PMCPMC4687624
OpenAlexW2204777433

What OpenQuestion holds

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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.