Evidence map›Paper›PMID 33093218›Full record

ArticleCancer immunology research2020

Pharmacologic Inhibition of FGFR Modulates the Metastatic Immune Microenvironment and Promotes Response to Immune Checkpoint Blockade.

Saeed S Akhand, Zian Liu, Stephen C Purdy, Ammara Abdullah, Hang Lin, Gregory M Cresswell, Timothy L Ratliff, Michael Wendt

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

31 citing papers in PubMed, 34 citations in OpenAlex.

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  7. Breast Cancer Progression by the FGF/FGFR Axis: A Metabolic Perspective.Journal of mammary gland biology and neoplasia · 2025
    Review
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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

8 authors at 1 institution in 1 country.

Saeed S AkhandDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana.
Zian LiuDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana.ORCID 0000-0003-4803-0906
Stephen C PurdyDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana.
Ammara AbdullahDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana.ORCID 0000-0003-4035-9790
Hang LinDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana.
Gregory M CresswellDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana.ORCID 0000-0003-0616-0366
Timothy L RatliffDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Indiana.ORCID 0000-0003-4221-5416
Michael WendtDepartment of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana. mwendt@purdue.edu.
Purdue University West Lafayette · US

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI John Tesmer · 1985 to 2026
$43.4M
Obesity, Metabolism and Breast Cancer MetastasisR01CA232589 · NCI · PURDUE UNIVERSITY · PI HURSTING, STEPHEN D, TEEGARDEN, DOROTHY · 2019 to 2023
$2.6M
Overcoming metastatic resistance to ErbB-targeted therapiesR01CA207751 · NCI · PURDUE UNIVERSITY · PI WENDT, MICHAEL KEITH · 2017 to 2021
$1.7M
The influence of alcohol on the metastatic dormancy of breast cancerR21AA026675 · NIAAA · PURDUE UNIVERSITY · PI VAN RIJN, RICHARD M., WENDT, MICHAEL KEITH · 2018 to 2019
$280k
NCI NIH HHS P30 CA023168NCI NIH HHS R01 CA207751NCI NIH HHS R01 CA232589NIAAA NIH HHS R21 AA026675
6 · The paper itself

Abstract

The effectiveness of immunotherapy as a treatment for metastatic breast cancer is limited due to low numbers of infiltrating lymphocytes in metastatic lesions. Herein, we demonstrated that adjuvant therapy using FIIN4, a covalent inhibitor of fibroblast growth factor receptor (FGFR), dramatically delayed the growth of pulmonary metastases in syngeneic models of metastatic breast cancer. In addition, we demonstrated in a syngeneic model of systemic tumor dormancy that targeting of FGFR enhanced the immunogenicity of the pulmonary tumor microenvironment through increased infiltration of CD8

Indexed as

AnimalsBreast NeoplasmsCD8-Positive T-LymphocytesCell Line, TumorChemokine CXCL16FemaleHumansImmune Checkpoint InhibitorsImmunotherapyMiceMice, Inbred BALB CMice, Inbred NODMice, NudeProgrammed Cell Death 1 ReceptorReceptor, Fibroblast Growth Factor, Type 1Signal TransductionChemokine CXCL16CXCL16 protein, humanImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorReceptor, Fibroblast Growth Factor, Type 1

Identifiers

PMID33093218
PMCPMC7710538
OpenAlexW3093764080

What OpenQuestion holds

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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.