Evidence map›Paper›PMID 38746359›Full record

ArticlebioRxiv : the preprint server for biology2024

Validation of ferroptosis in canine cancer cells to enable comparative oncology and translational medicine.

Priya Chatterji, Gang Xing, Laura Furst, Krishna Dave, Qiong Zhou, Daniel V LaBarbera, Douglas H Thamm, John K Eaton, Mathias J Wawer, Vasanthi S Viswanathan

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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.

Priya ChatterjiKojin Therapeutics, 451 D Street, Suite 502, Boston, MA 02210.ORCID 0000-0001-7792-9078
Gang XingKojin Therapeutics, 451 D Street, Suite 502, Boston, MA 02210.ORCID 0000-0001-8857-9421
Laura FurstKojin Therapeutics, 451 D Street, Suite 502, Boston, MA 02210.
Krishna DaveKojin Therapeutics, 451 D Street, Suite 502, Boston, MA 02210.
Qiong ZhouThe CU Anschutz Center for Drug Discovery, Skaggs School of Pharmacy and Pharmaceutical Sciences, Department of Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, 12850 E. Montview Blvd, Aurora, CO 80045.
Daniel V LaBarberaThe CU Anschutz Center for Drug Discovery, Skaggs School of Pharmacy and Pharmaceutical Sciences, Department of Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, 12850 E. Montview Blvd, Aurora, CO 80045.ORCID 0000-0001-9460-3862
Douglas H ThammFlint Animal Cancer Center, Colorado State University, 300 West Drake Road, Fort Collins, CO 80523.ORCID 0000-0002-8914-7767
John K EatonKojin Therapeutics, 451 D Street, Suite 502, Boston, MA 02210.ORCID 0000-0003-4633-5546
Mathias J WawerKojin Therapeutics, 451 D Street, Suite 502, Boston, MA 02210.ORCID 0000-0001-6664-0930
Vasanthi S ViswanathanKojin Therapeutics, 451 D Street, Suite 502, Boston, MA 02210.ORCID 0000-0001-9878-3629

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
NCI NIH HHS P30 CA046934
6 · The paper itself

Abstract

Ferroptosis is a cell death mechanism that has attracted significant attention as a potential basis for the development of new cancer therapies. Validation of ferroptosis biology in species commonly used in translation and pre-clinical development is a necessary foundation for enabling the advancement of such ferroptosis modulating drugs. Here, we demonstrate that canine cancer cells exhibit sensitivity to a wide range of ferroptosis-inducing perturbations in a manner indistinguishable from human cancer cells, and recapitulate characteristic patterns of ferroptotic response across tumor types seen in the human setting. The foundation provided herein establishes the dog as a relevant efficacy and toxicology model for ferroptosis and creates new opportunities to leverage the canine comparative oncology paradigm to accelerate the development of ferroptosis-inducing drugs for human cancer patients.

Identifiers

PMID38746359
PMCPMC11092520

What OpenQuestion holds

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Registered trials

None linked

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.