Evidence map›Paper›PMID 41223329›Full record

ArticleCancer research2026

Deep-Learning Tool ScVital Enables Species-Agnostic Integration of Cancer Cell States.

Jonathan Rub, Jason E Chan, Carleigh Sussman, Gary Guzman, William D Tap, Cristina R Antonescu, Samuel Singer, Tuomas Tammela, Doron Betel

Abstract read
In one paragraph

Article in Cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Jonathan RubTri-I Program in Computational Biology & Medicine, Weill Cornell Medicine, New York, New York.ORCID 0000-0001-8086-2310
Jason E ChanCancer Biology and Genetics Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-0552-8544
Carleigh SussmanCancer Biology and Genetics Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0009-0004-6230-6408
Gary GuzmanCancer Biology and Genetics Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-8002-9994
William D TapDivision of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0001-7779-2796
Cristina R AntonescuDivision of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0002-9717-8205
Samuel SingerDepartment of Surgery, Memorial Sloan Kettering Cancer Center and Weill Cornell Medical College, New York, New York.ORCID 0000-0001-9713-8230
Tuomas TammelaCancer Biology and Genetics Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.ORCID 0000-0003-3675-6961
Doron BetelDivision of Hematology & Medical Oncology, Department of Medicine, Weill Cornell Medicine, New York, New York.ORCID 0000-0002-8006-7752

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Division of Loan Repayment (DLR)Memorial Sloan-Kettering Cancer Center (MSK) P30-CA08748National Institutes of Health (NIH) 01-AG054720National Institutes of Health (NIH) K08-CA267072National Institutes of Health (NIH) R01-CA290400National Institutes of Health (NIH) T32-GM132083-02NCI NIH HHS L30 CA264322NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Genetically engineered mouse models (GEMM) of cancer are useful for exploring the development and biological composition of human tumors. Single-cell RNA sequencing (scRNA-seq) provides a transcriptomic snapshot of cancer to explore the heterogeneity of cell states in an immunocompetent context. However, cross-species comparison often suffers from biological batch effect, and inherent differences between species decrease the signal of biological insights that can be gleaned from these models. In this study, we developed scVital, a computational tool that uses a variational autoencoder and discriminator to embed scRNA-seq data into a species-agnostic latent space to overcome batch effect and identify cell states shared between species. In addition, latent space similarity score was concurrently developed as a new metric to evaluate batch correction accuracy by leveraging prelabeled clusters for scoring instead of the current method of creating new clusters. Using latent space similarity for quantification, scVital performed comparably well relative to other deep-learning algorithms and rapidly integrated scRNA-seq data of normal tissues across species with high fidelity. When scVital was applied to pancreatic ductal adenocarcinoma or lung adenocarcinoma data from GEMMs and primary patient samples, scVital accurately aligned biologically similar cell states. In undifferentiated pleomorphic sarcoma, a test case with no a priori knowledge of cell state concordance between mouse and human, scVital identified a previously unknown cell state that persisted after chemotherapy and is shared by a GEMM and human patient-derived xenografts. These findings establish the utility of scVital in identifying conserved cell states across species to enhance the translational capabilities of mouse models. SIGNIFICANCE: ScVital is an algorithm for cross-species integration of single-cell data to identify common cell states and facilitate translation of tumor models towards therapeutic application. This article is part of a special series: Driving Cancer Discoveries with Computational Research, Data Science, and Machine Learning/AI .

Indexed as

Carcinoma, Pancreatic DuctalDeep LearningPancreatic NeoplasmsSingle-Cell AnalysisAlgorithmsAnimalsComputational BiologyDisease Models, AnimalHumansMiceRNA-SeqSpecies Specificity

Identifiers

PMID41223329
PMCPMC13053053

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.