Evidence map›Paper›PMID 33826903›Full record

ArticleCell reports2021

Metabolic modulation by CDK4/6 inhibitor promotes chemokine-mediated recruitment of T cells into mammary tumors.

Roman V Uzhachenko, Vijaya Bharti, Zhufeng Ouyang, Ashlyn Blevins, Stacey Mont, Nabil Saleh, Hunter A Lawrence, Chengli Shen, Sheau-Chiann Chen, Gregory D Ayers and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

53 citing papers in PubMed, 94 citations in OpenAlex.

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  17. CYPD limits HRCell death discovery · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 1 country.

Roman V UzhachenkoComprehensive Cancer Center - James, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA; Department of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.
Vijaya BhartiComprehensive Cancer Center - James, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA; Department of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.
Zhufeng OuyangComprehensive Cancer Center - James, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA; Department of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.
Ashlyn BlevinsDepartment of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN 37212, USA.
Stacey MontDepartment of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN 37212, USA.
Nabil SalehDepartment of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN 37212, USA.
Hunter A LawrenceDepartment of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN 37212, USA.
Chengli ShenComprehensive Cancer Center - James, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.
Sheau-Chiann ChenDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN 37212, USA.
Gregory D AyersDepartment of Biostatistics, Vanderbilt University Medical Center, Nashville, TN 37212, USA.
David G DeNardoDepartment of Medicine, Washington University St. Louis, School of Medicine, St. Louis, MO 63110, USA.
Carlos ArteagaSimmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Ann RichmondDepartment of Pharmacology, Vanderbilt University School of Medicine, Nashville, TN 37212, USA; Department of Veterans Affairs, Tennessee Valley Healthcare System, Nashville, TN 37212, USA.
Anna E VilgelmComprehensive Cancer Center - James, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA; Department of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA. Electronic address: anna.vilgelm@osumc.edu.
The Ohio State University Wexner Medical Center · USVanderbilt University · USVanderbilt University Medical Center · USThe University of Texas Southwestern Medical Center · USWashington University in St. Louis · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
TISSUE CoreP50CA098131 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO, PIETENPOL, JENNIFER A · 2003 to 2024
$48.7M
Targeting the NF-kappaB Pathway in MelanomaR01CA116021 · NCI · VANDERBILT UNIVERSITY · PI RICHMOND, ANN, YAN, CHI · 2005 to 2024
$6.7M
Combining senescence-inducing and senolytic agents to improve melanoma therapyR37CA233770 · NCI · VANDERBILT UNIVERSITY · PI VILGELM, ANNA E · 2019 to 2025
$2.4M
Optimizing Response to Immune Checkpoint Inhibitor Therapy for Breast Cancer: A Role for Inhibitors of the PI3K pathwayR01CA243326 · NCI · VANDERBILT UNIVERSITY · PI RICHMOND, ANN, YAN, CHI · 2020 to 2024
$1.8M
BLR&D Merit Review Research Career Scientist (RCS) Award (IK6)IK6BX005225 · VA · VETERANS HEALTH ADMINISTRATION · PI RICHMOND, ANN · 2020 to 2023
–
Targeting IKK beta and aurora kinases in melanomaI01BX000196 · VA · VETERANS HEALTH ADMINISTRATION · PI RICHMOND, ANN · 2009 to 2013
–
BLRD VA I01 BX000196BLRD VA IK6 BX005225NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA068485NCI NIH HHS P50 CA098131NCI NIH HHS R01 CA116021NCI NIH HHS R01 CA243326NCI NIH HHS R37 CA233770
6 · The paper itself

Abstract

Inhibitors of cyclin-dependent kinases 4 and 6 (CDK4/6i) delay progression of metastatic breast cancer. However, complete responses are uncommon and tumors eventually relapse. Here, we show that CDK4/6i can enhance efficacy of T cell-based therapies, such as adoptive T cell transfer or T cell-activating antibodies anti-OX40/anti-4-1BB, in murine breast cancer models. This effect is driven by the induction of chemokines CCL5, CXCL9, and CXCL10 in CDK4/6i-treated tumor cells facilitating recruitment of activated CD8

Indexed as

AnimalsBreast NeoplasmsCell Line, TumorChemokinesCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6FemaleHumansHypertrophyImmunotherapyMammary Neoplasms, AnimalMiceMice, Inbred C57BLMitochondriaPrognosisProtein Kinase InhibitorsChemokinesCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Protein Kinase InhibitorsReactive Oxygen SpeciesReceptors, ChemokineTOR Serine-Threonine Kinasesadoptive cell transferanti-tumor immunitycancer metabolismCCL5CDK4/6 inhibitorschemokinesmetabolic stresspalbociclibROS

Identifiers

PMID33826903
PMCPMC8383195
OpenAlexW3141524818

What OpenQuestion holds

Textmetadata
LicenceTDM
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.