Evidence map›Paper›PMID 42227579›Full record

ArticleMolecular cancer therapeutics2026

Preclinical response of uveal melanomas to the velcrin compound, BAY 2666605.

Kristýna Kotýnková, Sawyer Andersen, Daniel Denney, Gizem Karsli Uzunbas, Miles Burri, Xiaoyun Wu, Bethany Kaplan, Rizwan Haq, Matthew Meyerson, Heidi Greulich

Abstract read
In one paragraph

Article in Molecular cancer therapeutics, 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

10 authors.

Kristýna KotýnkováBroad Institute Cambridge, MA United States.ORCID 0000-0003-2066-9505
Sawyer AndersenBroad Institute Cambridge, MA United States.ORCID 0009-0009-1828-4818
Daniel DenneyBroad Institute Cambridge, MA United States.ORCID 0009-0000-0565-5426
Gizem Karsli UzunbasBroad Institute Cambridge, MA United States.ORCID 0009-0007-5868-2592
Miles BurriBroad Institute Cambridge, MA United States.ORCID 0009-0002-7567-0263
Xiaoyun WuBroad Institute Cambridge, MA United States.ORCID 0009-0000-6021-480X
Bethany KaplanBroad Institute Cambridge, MA United States.ORCID 0009-0002-8503-7533
Rizwan HaqDana-Farber Cancer Institute Boston, MA United States.ORCID 0000-0002-1290-9276
Matthew MeyersonDana-Farber Cancer Institute Boston, MA United States.ORCID 0000-0002-9133-8108
Heidi GreulichBroad Institute Cambridge, MA United States.ORCID 0000-0001-5571-9862

Funding

Activation of SLFN12 RNase Activity by DimerizationR03CA293115 · NCI · BROAD INSTITUTE, INC. · PI GREULICH, HEIDI · 2024 to 2024
$154k
NCI NIH HHS R03 CA293115
6 · The paper itself

Abstract

Velcrin compounds kill cancer cells expressing elevated levels of two cellular proteins, the PDE3A phosphodiesterase and the SLFN12 tRNase, by inducing PDE3A-SLFN12 complex formation. This results in activation of SLFN12, leading to digestion of its specific substrate, tRNA-Leu-TAA, inhibition of protein synthesis, and cell death, a process now called "tomoptosis". We hypothesized that velcrins such as BAY 2666605, a clinical velcrin, could be active against biomarker-positive uveal melanomas. We identified uveal melanoma cell lines expressing elevated levels of the biomarkers, PDE3A and SLFN12, and tested response to velcrin compounds in vitro and in vivo. We show that response correlates mechanistically with decreased levels of tRNA-Leu-TAA and inhibition of nascent protein synthesis and furthermore identify a potential mechanism of resistance.

Identifiers

PMID42227579
PMCPMC13336339

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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.