Evidence map›Paper›PMID 26286831›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

A new application of plant virus nanoparticles as drug delivery in breast cancer.

Neda Esfandiari, Mohsen Karimi Arzanani, Masoud Soleimani, Mina Kohi-Habibi, Winnie E Svendsen

Abstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  6. Review
  7. Plant-Derived Anti-Cancer Therapeutics and Biopharmaceuticals.Bioengineering (Basel, Switzerland) · 2024
    Review
  8. Review
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  12. Review
  13. Self-assembled Viral Nanoparticles as Targeted Anticancer Vehicles.Biotechnology and bioprocess engineering : BBE · 2021
    Review
  14. Plant Virus Nanoparticles for Anti-cancer Therapy.Frontiers in bioengineering and biotechnology · 2021
    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

5 authors at 5 institutions in 3 countries.

Neda EsfandiariDepartment of Micro and Nanotechnology, Technical University of Denmark, Ørsteds Plads, 2800 Kgs, Lyngby, Denmark. neda.esfandiari@yahoo.com.
Mohsen Karimi ArzananiDivision of Hematology, Department of Medicine, Karolinska Institute, Karolinska University Hospital, SE14186, Stockholm, Sweden.
Masoud SoleimaniDepartment of Hematology, Faculty of Medical Science, Tarbiat Modares University, Tehran, Iran.
Mina Kohi-HabibiDepartment of Plant Protection, Faculty of Sciences and Plant Protection, Tehran University, Tehran, Iran.
Winnie E SvendsenDepartment of Micro and Nanotechnology, Technical University of Denmark, Ørsteds Plads, 2800 Kgs, Lyngby, Denmark.
Karolinska University Hospital · SEØrsted (Denmark) · DKTarbiat Modares University · IRTechnical University of Denmark · DKUniversity of Tehran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoparticles based on non-pathogenic viruses have opened up a novel sector in nanotechnology. Viral nanoparticles based on plant viruses have clear advantages over any synthetic nanoparticles as they are biocompatible and biodegradable self-assembled and can be produced inexpensively on a large scale. From several such under-development platforms, only a few have been characterized in the target-specific drugs into the cells. Potato virus X is presented as a carrier of the chemotherapeutic drug Herceptin that is currently used as a targeted therapy in (HER2+) breast cancer patients. Here, we used nanoparticles formed from the potato virus X to conjugate the Herceptin (Trastuzumab) monoclonal antibody as a new option in specific targeting of breast cancer. Bioconjugation was performed by EDC/sulfo-N-hydroxysuccinimide (sulfo-NHS) in a two-step protocol. Then, the efficiency of conjugation was investigated by different methods, including sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), Western blot, ELISA, Zetasizer, and transmission electron microscopy. SDS-PAGE and Western blot analysis confirmed an 82-kDa protein band that resulted from conjugation of potato virus X (PVX) coat protein (27 kDa) to heavy chain of Herceptin (55 kDa). Zeta potential values for conjugated particles, PVX, and HER were -7.05, -21.4, and -1.48, respectively. We investigated the efficiency of PVX-Herceptin to induce SK-OV-3 and SK-BR-3 cells (HER2 positive cell lines) apoptosis. We therefore counted cells and measured apoptosis by flow cytometry assay, then compared with Herceptin alone. Based on our data, we confirmed the conjugation of PVX and Herceptin. This study suggests that the PVX-Herceptin conjugates enable Herceptin to become more potential therapeutic tools.

Indexed as

PotexvirusAntineoplastic AgentsApoptosisBreast NeoplasmsCell Line, TumorDrug CarriersElectrophoresis, Polyacrylamide GelEnzyme-Linked Immunosorbent AssayErb-b2 Receptor Tyrosine KinasesFlow CytometryHumansMicroscopy, Electron, TransmissionNanoparticlesNicotianaTrastuzumabAntineoplastic AgentsDrug CarriersERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesTrastuzumabCancerHER2+ cell linesImmunological testPlant viral nanoparticles

Identifiers

PMID26286831
OpenAlexW1557701570

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.