Advances in Antitumor Research of Frizzled7 Inhibitors

Frizzled-7 (FZD7) is a key Wnt receptor that is frequently overexpressed in aggressive solid tumours and fuels therapy resistance. Over the past several years, a diverse arsenal of FZD7 inhibitors, including monoclonal antibodies, antibodydrug conjugates, bifunctional fusion proteins, small-molecule and peptideshas been discovered or synthesized by researchers, and it has been proven that tumor cell amplification or resuscitation can be controlled by inhibiting FZD7. Among them, Humanised antibody SHH002-hu1, the latest antibody targeting FZD7, achieves high affinity with low cross-reactivity. Yet no agent has progressed beyond phase Ib. After analyzing the latest researches, this article synthesise the current landscape, classifying inhibitors by modality, then provides a comprehensive reference for the new drug design of the target and suggests the future use direction of FZD7 inhibitors. In the future, the selectivity of targeted FZD7 antibodies may become the focus. At the same time, the combined drug use strategy of the target inhibitor with other anticancer drugs and the individualized medication method for different patients will also become the direction of research.

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Publication Details

Journal
Theoretical and Natural Science
Published
2025-09-09
DOI
https://doi.org/10.54254/2753-8818/2025.ld26553
Primary Topic
Microtubule and mitosis dynamics
Type
article
Field-Weighted Citation Impact
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article

Advances in Antitumor Research of Frizzled7 Inhibitors

Tianrui Zhu
Theoretical and Natural Science
Microtubule and mitosis dynamics
article

Advances in Antitumor Research of Frizzled7 Inhibitors

Tianrui Zhu
article en

Abstract

Frizzled-7 (FZD7) is a key Wnt receptor that is frequently overexpressed in aggressive solid tumours and fuels therapy resistance. Over the past several years, a diverse arsenal of FZD7 inhibitors, including monoclonal antibodies, antibodydrug conjugates, bifunctional fusion proteins, small-molecule and peptideshas been discovered or synthesized by researchers, and it has been proven that tumor cell amplification or resuscitation can be controlled by inhibiting FZD7. Among them, Humanised antibody SHH002-hu1, the latest antibody targeting FZD7, achieves high affinity with low cross-reactivity. Yet no agent has progressed beyond phase Ib. After analyzing the latest researches, this article synthesise the current landscape, classifying inhibitors by modality, then provides a comprehensive reference for the new drug design of the target and suggests the future use direction of FZD7 inhibitors. In the future, the selectivity of targeted FZD7 antibodies may become the focus. At the same time, the combined drug use strategy of the target inhibitor with other anticancer drugs and the individualized medication method for different patients will also become the direction of research.

Theoretical and Natural ScienceVol. 129(1)
Shanghai University of Medicine and Health Sciences (CN)
Openalex Percentile: Top 74%
Microtubule and mitosis dynamics
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