Evidence map›Paper›PMID 32102522›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2020

Inhibitory Effect of Polyclonal Antibodies Against HER3 Extracellular Subdomains on Breast Cancer Cell Lines.

Samaneh Mansouri-Fard, Mojgan Ghaedi, Mohammad-Reza Shokri, Tannaz Bahadori, Jalal Khoshnoodi, Forough Golsaz-Shirazi, Mahmood Jeddi-Tehrani, Mohammad Mehdi Amiri, Fazel Shokri

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2020. 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
0.3field-weighted citation impact, top 38% 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. Article
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 3 institutions in 1 country.

Samaneh Mansouri-FardDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Mojgan GhaediDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Mohammad-Reza ShokriDepartment of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Tannaz BahadoriDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Jalal KhoshnoodiDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Forough Golsaz-ShiraziDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Mahmood Jeddi-TehraniMonoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Mohammad Mehdi AmiriDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Fazel ShokriDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Tehran University of Medical Sciences · IRAcademic Center for Education, Culture and Research · IRIran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHuman epidermal growth factor receptor 3 (HER3) is a unique member of the tyrosine kinase receptors with an inactive kinase domain and is the preferable dimerization partner for HER2 which lead to potent tumorigenic signaling.

methodsIn this study, the expression plasmids coding for the human HER3 subdomains were transfected into CHO-K1 cells. Produced proteins were characterized by ELISA and SDS-PAGE. Rabbits were immunized and produced polyclonal antibodies (pAbs) that were characterized by ELISA, Immunoblotting and flowcytometry and their inhibitory effects were assessed by XTT on BT-474 and JIMT-1 breast cancer cell lines.

resultThe recombinant subdomains were highly immunogenic in rabbits. The pAbs reacted with the recombinant subdomains as well as commercial HER3 and the native receptor on tumor cell membranes and could significantly inhibit growth of Trastuzumab sensitive (BT-474) and resistant (JIMT-1) breast cancer cell lines in vitro.

conclusionIt seems that HER3 extra cellular domains (ECD) induce a strong anti-tumor antibody response and may prove to be potentially useful for immunotherapeutic applications.<br />.

Indexed as

AnimalsAntibodies, NeoplasmAntineoplastic Agents, ImmunologicalBreast NeoplasmsCell Line, TumorCHO CellsCricetulusDimerizationDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesHumansImmunization, SecondaryImmunoglobulin GIn Vitro TechniquesMicePlasmidsAntibodies, NeoplasmAntineoplastic Agents, ImmunologicalERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesERBB3 protein, humanImmunoglobulin GReceptor, ErbB-3breast cancerFusion proteinHER3Polyclonal antibody

Identifiers

PMID32102522
PMCPMC7332115
OpenAlexW3008407994

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.