The DOI matches its Crossref record; 97 of the 98 references it cites were found in a registry or an index.
Cell Permeable Stapled Peptide Inhibitor of Wnt Signaling that Targets β-Catenin Protein-Protein Interactions
Open accessAbstract
The Wnt signaling pathway plays a critical role in cell proliferation and differentiation, thus it is often associated with diseases such as cancers. Unfortunately, although attractive, developing anti-cancer strategy targeting Wnt signaling has been challenging given that the most attractive targets are involved in protein-protein interactions (PPIs). Here, we develop a stapled peptide inhibitor that targets the interaction between β-catenin and T cell factor/lymphoid enhancer-binding factor transcription factors, which are crucially involved in Wnt signaling. Our integrative approach combines peptide stapling to optimize proteolytic stability, with lessons learned from cell-penetrating peptide (CPP) design to maximize cellular uptake resulting in NLS-StAx-h, a selective, cell permeable, stapled peptide inhibitor of oncogenic Wnt signaling that efficiently inhibits β-catenin-transcription factor interactions. We expect that this type of integrative strategy that endows stapled peptides with CPP features will be generally useful for developing inhibitors of intracellular PPIs.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In addition, several compounds have been selected as inhibitors targeting β-cateninde PPI, including small molecules such as ICG-001 (176),448 NLs-StAx-h (177)449 and CRT inhibitors (iCRT3 (178), iCRT5 (179), iCRT14 (180)),450 Henryin (181),451 PKF115-584 (182) and CGP049090 (183).452”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [449]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Cox, J., & Mann, M. (2008) · Nature Biotechnology · doi:10.1038/nbt.1511 · Cited by 14,855
The Perseus computational platform for comprehensive analysis of (prote)omics data
Tyanova, S., Temu, T., Sinitcyn, P., Carlson, A., Hein, M. Y., Geiger, T., Mann, M., & Cox, J. (2016) · Nature Methods · doi:10.1038/nmeth.3901 · Cited by 8,803
Wnt/β-catenin signaling and disease
Clevers, H., & Nusse, R. (2012) · Cell · doi:10.1016/j.cell.2012.05.012 · Cited by 5,554
Cox, J., Hein, M. Y., Luber, C. A., Paron, I., Nagaraj, N., & Mann, M. (2014) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m113.031591 · Cited by 5,180
Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts
Sato, T., van Es, J. H., Snippert, H. J., Stange, D. E., Vries, R. G., van den Born, M., Barker, N., Shroyer, N. F., van de Wetering, M., & Clevers, H. (2011) · Nature · doi:10.1038/nature09637 · Cited by 2,510
COSMIC: exploring the world's knowledge of somatic mutations in human cancer
Forbes, S. A., Beare, D. M., Gunasekaran, P., Leung, K., Bindal, N., Boutselakis, H., Ding, M., Bamford, S., Cole, C. G., Ward, S. A., et al. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1075 · Cited by 2,294
Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling
Huang, S.-M. A., Mishina, Y., Liu, S.-M., Cheung, A. K., Stegmeier, F., Michaud, G., Charlat, O., Wiellette, E., Zhang, Y., Wiessner, S., et al. (2009) · Nature · doi:10.1038/nature08356 · Cited by 2,077
Cation-π interactions in structural biology
Gallivan, J. P., & Dougherty, D. A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.17.9459 · Cited by 2,005
Wender, P. A., Mitchell, D. J., Pattabiraman, K., Pelkey, E. T., Steinman, L., & Rothbard, J. B. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.24.13003 · Cited by 1,644
Richard, J., Melikov, K., Vivès, É., Ramos, C., Verbeure, B., Gait, M. J., Chernomordik, L., & Lebleu, B. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m209548200 · Cited by 1,454
Flagged first, then by citations
1 of the 98 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 101–133 of 133
Inhibition of Wnt Signaling Using Axin Peptidomimetics through Direct Targeting of β-Catenin
Sang, P., Wei, J., Qian, Y., Wu, M., Song, T., Li, W., Wei, J., Li, B., Zhang, J., Cai, J., et al. (2026) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6c00318 · Cited by 1
From Protein Structures to Functional Biomimetics
Grossmann, T. N., & Durukan, C. (2024) · Synlett · doi:10.1055/a-2308-1795 · Cited by 1
Self-citationNanoparticle-mediated delivery of peptide-based degraders enables targeted protein degradationPreprint
Alabi, C. A., Ghosal, S., Robertus, C. M., Wang, J., Chan, H., Alamgir, A., & Almonte, J. (2024) · Research Square · doi:10.21203/rs.3.rs-3797623/v1 · Cited by 1
STRUCTURAL AND FUNCTIONAL IMPACTS OF CHEMICAL MODIFICATIONS IN PEPTIDES AND SMALL PROTEINS
Werner, H. M. (2018) · D-Scholarship@Pitt (University of Pittsburgh)
Langel, Ü. (2019) · Springer eBooks · doi:10.1007/978-981-13-8747-0_4
Jiang, S., & Brown, C. J. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.2210/pdb6kzu/pdb
Classes, Modes of Action and Selection of New Modalities in Drug Discovery
Valeur, E. (2020) · Royal Society of Chemistry eBooks · doi:10.1039/9781839160691-00277
Langel, Ü. (2019) · Springer eBooks · doi:10.1007/978-981-13-8747-0_1
Kannan, S., Aronica, P. G. A., Ng, S., Thean, D., Frosi, Y., Chee, S. M. Q., Jiang, S., Yuen, T. Y., Sadruddin, A., Kaan, H. Y. K., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/767673
Identification of an H-Ras nanocluster disrupting peptidePreprint
Manoharan, G. B., Steffen, C. L., Pavic, K., Yeste‐Vázquez, A., Knuuttila, M., Arora, N., Zhou, Y., Härmä, H., Gaigneaux, A., Grossmann, T. N., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.07.556635
Self-citationLangel, Ü. (2023) · Springer eBooks · doi:10.1007/978-3-031-38731-9_1
Langel, Ü. (2023) · Springer eBooks · doi:10.1007/978-3-031-38731-9_7
New Therapeutic Chemical Modalities: Compositions, Modes-of-action, and Drug Discovery
Valeur, E. (2023) · Royal Society of Chemistry eBooks · doi:10.1039/9781788018982-00911
Integrated Anchored Stapling and Hierarchical Dynamics: MSICDA-Driven CREBBP Bromodomain Inhibition
Wang, X., Chen, X., Chen, Z., Xu, W., Lai, R., Qiu, X., Zeng, Z., Wang, C., Wang, Z., & Wang, J. (2024) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.4c00381
Pi, J. H., Choi, S. Y., Park, S.-K., Lim, J., & Kang, C.-J. (2025) · Molecular Therapy Oncology · doi:10.1016/j.omton.2025.200953
Molecular mechanisms and clinical implications of Wnt pathway inhibition
Wang, R., & Wang, P. (2025) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2025.152806
Mechanistic design of cell-penetrating disruptors for phospho-dependent TACC3-CHC interaction
Gunning, V., Batchelor, M. R., Alexander, K. K., Walko, M., Dill, T. C., Burgess, S. G., Royle, S., Kennedy, E. J., & Bayliss, R. W. (2026) · Structure · doi:10.1016/j.str.2026.04.001
Recent advances in the molecular interactions of anti-cancer peptides with cellular targets
Zaeifi, D. (2026) · Life Sciences · doi:10.1016/j.lfs.2026.124454
Mosalam, E. M., Abdallah, M. S., Gardouh, A. R., Hamza, E., Bahaa, M. M., Nazih, M., Al-Dhelaan, R. A., & Kamal, N. (2026) · Journal of Pharmacy & Pharmaceutical Sciences · doi:10.3389/jpps.2026.16610
Li, B., Perrin, M. E., Maillard, E., Vitard, A., Moal, G., Mbianda, J., André, C., Nunes, M. T., Vandamme, M., Pinna, G., et al. (2026) · Angewandte Chemie · doi:10.1002/ange.4112426
Li, B., Perrin, M. E., Maillard, E., Vitard, A., Moal, G., Mbianda, J., André, C., Nunes, M. T., Vandamme, M., Pinna, G., et al. (2026) · Angewandte Chemie International Edition · doi:10.1002/anie.4112426
Meulendijks, M. H. N., Li, Y., Steiner, F. J., Klintrot, R., Schulte, C., Roose, S., Yeste‐Vázquez, A., Maric, H. M., Hennig, S., Paulussen, F. M., et al. (2026) · ChemistryEurope · doi:10.1002/ceur.70357
Self-citationPeptide-protein interactions in drug discovery
Ying, H., Lei, Y., Luo, Y., Zeng, J., & de la Fuente‐Núñez, C. (2026) · Cell Biomaterials · doi:10.1016/j.celbio.2026.100598
BindingDB Entry 50019686: Stapled Peptides as Direct Inhibitors of Nrf2-sMAF Transcription Factors.
BindingDB (2024) · UC San Diego · doi:10.7270/q2qj7np4
Metadata
- Authors
- Dietrich, L., Rathmer, B., Ewan, K., Bange, T., Heinrichs, S., Dale, T. C., Schade, D., & Grossmann, T. N.
- Affiliations
- Max Planck Society (DE)
- TU Dortmund University (DE)
- Cardiff University (GB)
- Max Planck Institute of Molecular Physiology (DE)
- Essen University Hospital (DE)
- Corresponding author
- Grossmann, Tom N.
- Venue
- Cell Chemical Biology
- Publisher
- Elsevier BV
- Published
- 2017-08
- Volume
- 24
- Issue
- 8
- Pages
- 958-968.e5
- ISSN
- 2451-9448 (ISSN-L)
- 2451-9456
- OpenAlex
- W2741166200
- Cited by
- 126
- References
- 98
- Citations by year
- 2026: 10 · 2025: 4 · 2024: 23 · 2023: 12 · 2022: 13 · 2021: 19 · 2020: 14 · 2019: 14 · 2018: 16 · 2017: 1
- FWCI
- 5.14
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell chemical biology (publishedVersion)
- PubMed (publishedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (acceptedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- VU Research Portal (submittedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Funders
- Max-Planck-Gesellschaft
- Cancer Research UK (C368/A4545, C368/A7990)
- AstraZeneca
- European Research Council (678623)
- Boehringer Ingelheim
- Bayer HealthCare
- Bayer CropScience
- Deutsche Forschungsgemeinschaft (GR3592/2-1)
- Bundesministerium für Bildung und Forschung (131605)
- Biotechnology and Biological Sciences Research Council (BB/D00117X/1)
- Merck KGaA
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Keywords
- Wnt signaling, β-catenin, protein-protein interaction inhibitors, stapled peptides, cell-penetrating peptides, T-cell factor, nuclear localization signal, membrane permeability, cancer therapy
- MeSH terms
- Amino Acid Sequence, Cell Membrane Permeability, Cell Movement, HeLa Cells, Humans, Gene Expression, Genes, Reporter, Microscopy, Confocal, Cell Line, Tumor, Cell Proliferation, beta Catenin, Basic Helix-Loop-Helix Transcription Factors, Basic Helix-Loop-Helix Proteins, Protein Interaction Domains and Motifs, Cell-Penetrating Peptides, Wnt Signaling Pathway, Axin Protein
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review