Evidence map›Paper›PMID 42085373›Full record

ArticlePloS one2026

EGFR-targeted affibody-polyIC polyplex kills EGFR-overexpressing cancer cells without activating the EGFR.

Anne Pettikiriarachchi, Yelena Ugolev, Richard Birkinshaw, Ahmad Wardak, Maree C Faux, Timothy E Adams, Salim Joubran, Alexei Shir, Nufar Edinger, Maya Zigler and 2 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Anne PettikiriarachchiPersonal Oncology, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Yelena UgolevUnit of Cellular Signaling, Silberman Life Sciences Institute, The Hebrew University of Jerusalem, Jerusalem, Israel.
Richard BirkinshawStructural Biology, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Ahmad WardakStructural Biology, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Maree C FauxPersonal Oncology, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.
Timothy E AdamsCSIRO Manufacturing, Clayton, Victoria, Australia.
Salim JoubranUnit of Cellular Signaling, Silberman Life Sciences Institute, The Hebrew University of Jerusalem, Jerusalem, Israel.
Alexei ShirUnit of Cellular Signaling, Silberman Life Sciences Institute, The Hebrew University of Jerusalem, Jerusalem, Israel.
Nufar EdingerUnit of Cellular Signaling, Silberman Life Sciences Institute, The Hebrew University of Jerusalem, Jerusalem, Israel.
Maya ZiglerUnit of Cellular Signaling, Silberman Life Sciences Institute, The Hebrew University of Jerusalem, Jerusalem, Israel.
Alexander LevitzkiUnit of Cellular Signaling, Silberman Life Sciences Institute, The Hebrew University of Jerusalem, Jerusalem, Israel.
Antony W BurgessPersonal Oncology, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia.ORCID https://orcid.org/0000-0003-3275-9209

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epidermal growth factor receptor (EGFR) is aberrantly activated in many human epithelial cancers. This report presents the preparation, purification, and the anti-cancer potency of an anti-EGFR affibody (ZEGFR 1907')-polyethylenimine (PEI)-polyIC complex (PPEA-polyplex). Surface plasmon resonance analysis showed that the ZEGFR 1907' affibody binds tightly to full-length sEGFR with an average equilibrium dissociation constant, KD, value of 6.74 nM. As expected the PPEA-polyplex does not activate the EGFR kinase, but kills tumor cells expressing medium to high levels of EGFR. The PPEA-polyplex stimulates the release of chemotactic cytokines (e.g., GRO-α, IFN-γ-inducible protein-10) and promoted PBMC-mediated bystander killing of non-treated tumor cells. The PPEA-polyplex also inhibited the growth of human epidermoid vulval carcinoma (A431) xenografts growing in immunocompromised nude mice. Both the in vitro and in vivo results indicate that PPEA-polyplexes have the potential to inhibit the growth of tumors which over-express the EGFR, including colon and breast cancer cells.

Indexed as

ErbB ReceptorsNeoplasmsPolyethyleneimineRecombinant Fusion ProteinsAnimalsCell Line, TumorFemaleHumansMiceMice, NudeXenograft Model Antitumor AssaysErbB ReceptorsPolyethyleneimineRecombinant Fusion Proteins

Identifiers

PMID42085373
PMCPMC13143101

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Registered trials

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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.