Evidence map›Paper›PMID 38581448›Full record

ArticleCancer research2024

Integration of Pan-Cancer Cell Line and Single-Cell Transcriptomic Profiles Enables Inference of Therapeutic Vulnerabilities in Heterogeneous Tumors.

Weijie Zhang, Danielle Maeser, Adam Lee, Yingbo Huang, Robert F Gruener, Israa G Abdelbar, Sampreeti Jena, Anand G Patel, R Stephanie Huang

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

15 citing papers in PubMed, 17 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Weijie Zhang *Bioinformatics and Computational Biology, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-8978-8310
Danielle Maeser *Bioinformatics and Computational Biology, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-3890-887X
Adam LeeDepartment of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-8311-581X
Yingbo HuangDepartment of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-3973-4277
Robert F GruenerDepartment of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-8166-2772
Israa G AbdelbarDepartment of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota.ORCID 0009-0007-3558-7330
Sampreeti JenaDepartment of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota.ORCID 0009-0005-5462-6046
Anand G PatelDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-1438-8275
R Stephanie HuangBioinformatics and Computational Biology, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0002-9862-0368
University of Minnesota · USSt. Jude Children's Research Hospital · US

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI BRISCOE, LYNN · 2019 to 2025
$3932.6M
Genetic mechanisms underlying sexual dimorphism in cancer and response to therapyR01CA229618 · NCI · UNIVERSITY OF COLORADO DENVER · PI HUANG, RONG STEPHANIE, STRANGER, BARBARA E · 2019 to 2024
$2.9M
Drug repurposing in breast cancerR01CA204856 · NCI · UNIVERSITY OF MINNESOTA · PI HUANG, RONG STEPHANIE · 2018 to 2022
$2.2M
Clinical and Translational Science Institute, University of Minnesota (CTSI) A-PRePGraduate School, University of Minnesota (The Graduate School, University of Minnesota) DDFGraduate School, University of Minnesota (The Graduate School, University of Minnesota) IDFNational Cancer Institute (NCI) R01CA204856National Cancer Institute (NCI) R01CA229618NCI NIH HHS 75N91019D00024NCI NIH HHS R01 CA204856NCI NIH HHS R01 CA229618University of Minnesota (UMN) BICB FellowshipUniversity of Minnesota (UMN) OACA grants
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) greatly advanced the understanding of intratumoral heterogeneity by identifying distinct cancer cell subpopulations. However, translating biological differences into treatment strategies is challenging due to a lack of tools to facilitate efficient drug discovery that tackles heterogeneous tumors. Developing such approaches requires accurate prediction of drug response at the single-cell level to offer therapeutic options to specific cell subpopulations. Here, we developed a transparent computational framework (nicknamed scIDUC) to predict therapeutic efficacies on an individual cell basis by integrating single-cell transcriptomic profiles with large, data-rich pan-cancer cell line screening data sets. This method achieved high accuracy in separating cells into their correct cellular drug response statuses. In three distinct prospective tests covering different diseases (rhabdomyosarcoma, pancreatic ductal adenocarcinoma, and castration-resistant prostate cancer), the predicted results using scIDUC were accurate and mirrored biological expectations. In the first two tests, the framework identified drugs for cell subpopulations that were resistant to standard-of-care (SOC) therapies due to intrinsic resistance or tumor microenvironmental effects, and the results showed high consistency with experimental findings from the original studies. In the third test using newly generated SOC therapy-resistant cell lines, scIDUC identified efficacious drugs for the resistant line, and the predictions were validated with in vitro experiments. Together, this study demonstrates the potential of scIDUC to quickly translate scRNA-seq data into drug responses for individual cells, displaying the potential as a tool to improve the treatment of heterogenous tumors. SIGNIFICANCE: A versatile method that infers cell-level drug response in scRNA-seq data facilitates the development of therapeutic strategies to target heterogeneous subpopulations within a tumor and address issues such as treatment failure and resistance.

Indexed as

Single-Cell AnalysisTranscriptomeAntineoplastic AgentsCarcinoma, Pancreatic DuctalCell Line, TumorDrug Resistance, NeoplasmGene Expression ProfilingHumansMaleNeoplasmsPancreatic NeoplasmsProstatic Neoplasms, Castration-ResistantRhabdomyosarcomaRNA-SeqSequence Analysis, RNATumor MicroenvironmentAntineoplastic Agents

Identifiers

PMID38581448
PMCPMC11178452
OpenAlexW4394014190

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.