Evidence map›Paper›PMID 38885192›Full record

ArticlePLoS genetics2024

Single-cell analysis identifies PLK1 as a driver of immunosuppressive tumor microenvironment in LUAD.

Yifan Kong, Chaohao Li, Jinpeng Liu, Sai Wu, Min Zhang, Derek B Allison, Faisal Hassan, Daheng He, Xinyi Wang, Fengyi Mao and 5 more

Abstract read
In one paragraph

Article in PLoS genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Yifan KongDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.
Chaohao LiDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.
Jinpeng LiuMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America.
Sai WuDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.
Min ZhangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.
Derek B AllisonMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America.ORCID 0000-0002-5119-2474
Faisal HassanDepartment of Pathology and Laboratory Medicine, University of Kentucky, Lexington, Kentucky, United States of America.
Daheng HeMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America.ORCID 0000-0003-0399-2466
Xinyi WangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.ORCID 0000-0002-8869-8292
Fengyi MaoDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.
Qiongsi ZhangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.
Yanquan ZhangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.
Zhiguo LiDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.
Chi WangMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America.
Xiaoqi LiuDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, Kentucky, United States of America.ORCID 0000-0002-6613-1746

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers · 2013 to 2026
$38.3M
Institutional Career Development CoreKL2TR001996 · NCATS · UNIVERSITY OF KENTUCKY · PI BUSH, MATTHEW LEE, KELLY, THOMAS H. · 2016 to 2025
$7.1M
Plk1 in Chemo-resistance of CancerR01CA157429 · NCI · UNIVERSITY OF KENTUCKY · PI XIAOQI LIU · 2011 to 2026
$3.5M
Improving chemotherapy of castration-resistant prostate cancer.R01CA196634 · NCI · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI · 2016 to 2025
$3.3M
Plk1 as a prognostic biomarker for prostate cancerR01CA264652 · NCI · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI · 2021 to 2025
$2.7M
Enhancing the efficacy of androgen signaling inhibitors in prostate cancerR01CA256893 · NCI · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI · 2021 to 2025
$2.4M
NCATS NIH HHS KL2 TR001996NCI NIH HHS P30 CA177558NCI NIH HHS R01 CA157429NCI NIH HHS R01 CA196634NCI NIH HHS R01 CA256893NCI NIH HHS R01 CA264652
6 · The paper itself

Abstract

PLK1 (Polo-like kinase 1) plays a critical role in the progression of lung adenocarcinoma (LUAD). Recent studies have unveiled that targeting PLK1 improves the efficacy of immunotherapy, highlighting its important role in the regulation of tumor immunity. Nevertheless, our understanding of the intricate interplay between PLK1 and the tumor microenvironment (TME) remains incomplete. Here, using genetically engineered mouse model and single-cell RNA-seq analysis, we report that PLK1 promotes an immunosuppressive TME in LUAD, characterized with enhanced M2 polarization of tumor associated macrophages (TAM) and dampened antigen presentation process. Mechanistically, elevated PLK1 coincides with increased secretion of CXCL2 cytokine, which promotes M2 polarization of TAM and diminishes expression of class II major histocompatibility complex (MHC-II) in professional antigen-presenting cells. Furthermore, PLK1 negatively regulates MHC-II expression in cancer cells, which has been shown to be associated with compromised tumor immunity and unfavorable patient outcomes. Taken together, our results reveal PLK1 as a novel modulator of TME in LUAD and provide possible therapeutic interventions.

Indexed as

Adenocarcinoma of LungCell Cycle ProteinsLung NeoplasmsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsSingle-Cell AnalysisTumor MicroenvironmentAnimalsAntigen PresentationCell Line, TumorChemokine CXCL2Gene Expression Regulation, NeoplasticHistocompatibility Antigens Class IIHumansMiceCell Cycle ProteinsChemokine CXCL2Histocompatibility Antigens Class IIPlk1 protein, mousePolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene Proteins

Identifiers

PMID38885192
PMCPMC11182521

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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.