Evidence map›Paper›PMID 37034891›Full record

ArticleAvicenna journal of medical biotechnology

Cell Surface Vimentin Detection in Cancer Cells by Peptide-Based Monoclonal Antibody.

Niloufar Sadeghi, Ghazaleh Fazli, Ali Ahmad Bayat, Raminasadat Fatemi, Nasim Ebrahimnejhad, Ali Salimi, Omid Zarei, Hodjattallah Rabbani

Open access · greenAbstract read
In one paragraph

Article in Avicenna journal of medical biotechnology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
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

8 authors at 2 institutions in 1 country.

Niloufar SadeghiMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Ghazaleh FazliMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Ali Ahmad BayatMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Raminasadat FatemiMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Nasim EbrahimnejhadMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Ali SalimiMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Omid ZareiCellular and Molecular Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Hodjattallah RabbaniMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Academic Center for Education, Culture and Research · IRKurdistan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Vimentin is a prominent Intermediate Filaments (IFs) protein expressed in different mesenchymal origin cell types. Besides a wide range of cellular function roles associated with vimentin expression, its dysregulation and cell surface expression in the induction of malignancy properties have been reported extensively, making it a promising cancer-specific target. Therefore, this study aimed to generate and characterize anti-vimentin monoclonal antibodies. Methods: A 14-mer synthetic peptide from vimentin was conjugated to Keyhole Limpet Hemocyanin (KLH) and used for immunization of Blab/C mice and monoclonal production by conventional hybridoma technology. The monoclonal antibody was purified using affinity chromatography of supernatants from the selected hybridoma cells. ELISA, Immunoprecipitation-Western blotting (IP-WB), Immunocytochemistry (ICC), and flow cytometry were employed to characterize the produced monoclonal antibody in terms of interaction with vimentin immunizing peptide as well as vimentin protein. Results: Amid the several obtained producing anti-vimentin antibody hybridomas, the 7C11-D9 clone (IgG1 isotype with kappa light chain) showed higher reactivity with the immunizing peptide, and led to its selection for purification and characterization. The purified antibody could detect vimentin protein in IP-WB, ICC and flow cytometry of the normal and cancerous cells with different origin. No vimentin expression was found in normal healthy Peripheral Blood Mononuclear Cell (PBMC). Conclusion: Taken together, 7C11-D9 anti-vimentin monoclonal antibody might be used as immune diagnostic or immune therapeutic tool where detection or targeting of vimentin in a wide range of organisms is required.

Indexed as

AntibodyCancerPeptideTargeted therapyVimentin

Identifiers

PMID37034891
PMCPMC10073919
OpenAlexW4322100265

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.