Evidence map›Paper›PMID 39122876›Full record

ArticleBreast cancer (Tokyo, Japan)2024

Targeted therapies in HER2-positive breast cancer with receptor-redirected Arazyme-linker-Herceptin as a novel fusion protein.

Farideh Rahmani, Hatef Ajoudanifar, Nazila Arbab Soleimani, Abbas Ali Imani Fooladi

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Article in Breast cancer (Tokyo, Japan), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Farideh RahmaniDepartment of Microbiology, Damghan Branch, Islamic Azad University, Damghan, Iran.
Hatef AjoudanifarDepartment of Microbiology, Damghan Branch, Islamic Azad University, Damghan, Iran.
Nazila Arbab SoleimaniDepartment of Microbiology, Damghan Branch, Islamic Azad University, Damghan, Iran.
Abbas Ali Imani FooladiApplied Microbiology Research Center, Biomedicine Technologies Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran. imanifouladi.a@gmail.com.ORCID http://orcid.org/0000-0001-7339-8257

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTargeted treatment of different types of cancers through highly expressed cancer cell surface receptors by fusion proteins is an efficient method for cancer therapy. The HER2 receptor is a member of the tyrosine kinase receptors family, which plays a notable role in breast cancer tumor development. About 25-30% of breast cancers overexpress human epidermal growth factor receptor 2 (HER2).

methodsIn this study, we evaluated the particulars of a designed recombinant protein formed by HER2-specific Mab Herceptin linked with Arazyme on a HER2-overexpressing breast cancer cell line (SKBR3). Arazyme, a metalloprotease produced by Serratia proteamaculans was fused to the variable area of light and heavy chains of the Herceptin. The cytotoxic assay of the Arazyme-linker-Herceptin in the SKBR3 and MDA-MB-468 cells was evaluated by the MTT and flow cytometry techniques. The Caspase‑3 activity determination and adhesion assay were performed to evaluate the antitumor activity of the Arazyme-linker-Herceptin against SKBR3 cells. Furthermore, RT-PCR was used to measure the expression levels of the Bcl-2, Bax, MMP2, MMP9, and RIP3 genes.

resultsThe Arazyme-linker-Herceptin showed higher cytotoxicity in SKBR3 cells compared to MDA-MB-468 cells. In addition, flow cytometry results revealed that the Arazyme-linker-Herceptin can significantly induce apoptosis in the HER2-overexpressing breast cancer cell line (SKBR3), which was confirmed by Bax upregulation and the decrease in adhesion of tumor cells and MMP2/MMP9.

conclusionThe findings of this study demonstrated that the Arazyme-linker-Herceptin induced apoptosis and decreased metastatic genes in SKBR3 cells; however, further research is required to confirm the effectiveness of the fusion protein.

Indexed as

ApoptosisBreast NeoplasmsErb-b2 Receptor Tyrosine KinasesRecombinant Fusion ProteinsTrastuzumabAntineoplastic Agents, ImmunologicalCell Line, TumorFemaleHumansMatrix Metalloproteinase 2Matrix Metalloproteinase 9Molecular Targeted TherapyAntineoplastic Agents, ImmunologicalERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesMatrix Metalloproteinase 2Matrix Metalloproteinase 9Recombinant Fusion ProteinsTrastuzumabApoptosisArazyme-linker-HerceptinBreast cancerCytotoxicityHER2Targeting cancer

Identifiers

PMID39122876

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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.