Evidence map›Paper›PMID 40909631›Full record

ArticlebioRxiv : the preprint server for biology2025

Positive Selection Screen for Natural Product β-Catenin Inactivators.

Matthew W Boudreau, Vitor F Freire, Sophie C Corbett, Lucero Martínez-Fructuoso, Rohitesh Kumar, Christopher C Thornburg, Rhone K Akee, Brian D Peyser, Qinqin Jiang, Jennifer Splaine and 12 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 · Who and what money

Authors and funding

22 authors.

Matthew W BoudreauDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.ORCID 0000-0002-2116-1167
Vitor F FreireNatural Products Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Frederick, MD.
Sophie C CorbettDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
Lucero Martínez-FructuosoNatural Products Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Frederick, MD.
Rohitesh KumarNatural Products Support Group, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD.
Christopher C ThornburgNatural Products Support Group, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD.
Rhone K AkeeNatural Products Support Group, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD.
Brian D PeyserNatural Products Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Frederick, MD.
Qinqin JiangDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
Jennifer SplaineICCB-Longwood Screening Facility, Harvard Medical School, Boston, MA.
Jamie L PfaffDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
Benjamin C ChandlerDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
Dinah M AbejaDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA.
Katherine A DonovanDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA.
Jianwei CheDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA.
Benjamin L LampsonDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.
Patricia SzajnerICCB-Longwood Screening Facility, Harvard Medical School, Boston, MA.
Jennifer A SmithICCB-Longwood Screening Facility, Harvard Medical School, Boston, MA.
Vidyasagar KoduriDivision of Hematology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.
Tanja GrkovicNatural Products Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Frederick, MD.
Barry R O'KeefeNatural Products Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Frederick, MD.
William G KaelinDepartment of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA.ORCID 0000-0002-0574-4856

Funding

The von Hippel-Lindau Tumor Suppressor Gene and Kidney Cancer: Insights into Oxygen Sensing and Treating Cancers Caused by Undruggable MutationsR35CA210068 · NCI · DANA-FARBER CANCER INST · PI WILLIAM G. KAELIN · 2016 to 2026
$10.8M
NCI Program for Natural Products Discovery - CuresZIABC011854 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI OKEEFE, BARRY · 2020 to 2025
$5.2M
Mechanism of Action of Spautin-1, A Novel Degrader of IKZF1K08CA252611 · NCI · DANA-FARBER CANCER INST · PI KODURI, VIDYASAGAR · 2020 to 2024
$1.1M
Targeting Oncogenic Drivers in CancerK00CA253731 · NCI · DANA-FARBER CANCER INST · PI BOUDREAU, MATTHEW W · 2022 to 2025
$365k
CCR NIH HHS HHSN261200800001CIntramural NIH HHS ZIA BC011854NCI NIH HHS HHSN261200800001ENCI NIH HHS K00 CA253731NCI NIH HHS K08 CA252611NCI NIH HHS R35 CA210068
6 · The paper itself

Abstract

Cell-based phenotypic screening of natural product mixtures can reveal new biological and pharmacological principles but has been largely abandoned, partly because such mixtures can be difficult to deconvolute and often contain toxins that confound "down" assays. We reasoned that these concerns could be partly mitigated by screening prefractionated natural product mixtures in cell-based "up" assays. We tested 326,304 natural product mixtures (40,744 extracts and 285,560 fractions derived from them) in a high throughput screen using mammalian cells expressing an oncogenic version of β-catenin (β-cat) fused to a suicide protein. Multiple fractions degraded the β-cat fusion protein or drove it into a compartment where both fusion partners were apparently inactive. The active compound from one of the latter specifically activates novel, but not classical, protein kinase Cs (PKCs) and thereby relocates β-cat to juxtamembrane vacuolar structures. These findings suggest a path for inactivating oncogenic β-cat and underscore the power of natural product screening.

Identifiers

PMID40909631
PMCPMC12407916

What OpenQuestion holds

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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.