Evidence map›Paper›PMID 41069407›Full record

ArticleFrontiers in bioengineering and biotechnology2025

A novel Frizzled 7 antibody disrupts the Wnt pathway and inhibits Wilms tumor growth.

Einav Vax, Revital Caspi, Rachel Shukrun, Naomi Pode-Shakked, Oren Pleniceanu, Hana Golan, Michael Namestnikov, Michal Mark-Danieli, Ela Markovsky, Dekel D Bar-Lev and 5 more

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2025. 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
–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

2 citing papers in PubMed.

  1. Review
  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

15 authors.

Einav VaxPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Revital CaspiPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Rachel ShukrunPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Naomi Pode-ShakkedPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Oren PleniceanuPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Hana GolanPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Michael NamestnikovPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Michal Mark-DanieliPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Ela MarkovskyDepartment of Physiology and Pharmacology / Cancer Research and Nanomedicine, School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Dekel D Bar-LevPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Iris BarshackDepartment of Pathology, Sheba Medical Center, Ramat Gan, Israel.
Ronit Satchi-FainaroDepartment of Physiology and Pharmacology / Cancer Research and Nanomedicine, School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Orit Harari-SteinbergPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Sanja GoldbergPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Benjamin DekelPediatric Stem Cell Research Institute, Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Frizzled 7 (FZD7), a Wnt receptor that activates canonical Wnt/β-catenin signaling, has been implicated in multiple cancers, including Wilms tumor (WT), the most common pediatric kidney malignancy. We previously identified FZD7 as a marker of the WT cancer stem cell population and a potential therapeutic target. To evaluate this, we generated a panel of monoclonal anti-FZD7 antibodies using epitope mapping of the receptor and assessed their functional activity in primary WT cells and xenograft models. Among the panel, clone 288.1 induced significant cell death in primary Wilms tumor cells and inhibited cell proliferation and migration. This effect correlated with canonical Wnt signaling inhibition, a reduction in activated β-catenin and downregulation of Wnt/β-catenin target genes concomitant with diminished Wilms tumor cancer stem cell (CSC) markers. In vivo, treatment with anti-FZD7-288.1 significantly inhibited WT xenograft growth, resulting in reduced tumor volume. These findings demonstrate that FZD7 is a critical driver of Wilms tumor progression and support antibody-mediated FZD7 blockade as a promising therapeutic strategy.

Indexed as

anti-Frizzled 7 antibodycancer stem cellsFrizzled 7monoclonal antibody therapypediatric kidney cancertargeted therapyWilms tumorWnt/β-catenin signaling

Identifiers

PMID41069407
PMCPMC12504202

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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.