Evidence map›Paper›PMID 39644862›Full record

ArticleOral oncology2025

Targeting macrophage migration inhibitory factor to inhibit T cell immunosuppression in the tumor microenvironment and improve cancer outcomes in head and neck squamous cell carcinoma.

S Hasan Pracha, Suvekshya Shrestha, Nathan Ryan, Puja Upadhaya, Felipe F Lamenza, Sushmitha Jagadeesha, Pete Jordanides, Peyton Roth, Anna Springer, Steve Oghumu

Abstract read
In one paragraph

Article in Oral oncology, 2025. 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

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

10 authors.

S Hasan PrachaDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Suvekshya ShresthaDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA; Department of Microbiology, The Ohio State University, Columbus, OH, USA.
Nathan RyanDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Puja UpadhayaDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Felipe F LamenzaDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA; Department of Microbiology, The Ohio State University, Columbus, OH, USA.
Sushmitha JagadeeshaDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Pete JordanidesDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Peyton RothDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Anna SpringerDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Steve OghumuDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA. Electronic address: oghumu.1@osu.edu.

Funding

Mechanisms of Oral Cancer Inhibition by Bioactive Phytochemicals in Black RaspberriesK01CA207599 · NCI · OHIO STATE UNIVERSITY · PI OGHUMU, STEVE ONYEKA · 2017 to 2021
$715k
American Cancer Society (ACS) RSG-19079-01-TBGNCI NIH HHS K01 CA207599
6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) is the 7th most common cancer globally with a 40-50 % survival rate. Although macrophage migration inhibitory factor (MIF) is overexpressed in most solid tumors and promotes tumor growth and invasion, the therapeutic potential of MIF inhibition in HNSCC is yet to be explored. In this study, we investigated the efficacy of CPSI-1306, a small-molecule MIF inhibitor, on HNSCC cell growth and cancer associated signaling pathways in vitro, as well as its impact on T cells in the HNSCC tumor microenvironment in vivo. CPSI-1306 did not reduce HNSCC cell proliferation in vitro, and mildly decreased VEGF and EGFR expression. However, CPSI-1306 significantly reduced tumor development in two orthotopic mouse oral cancer (MOC-2 and MOC-1) HNSCC models. Interestingly, CPSI-1306 treatment increased T cell infiltration to the tumor microenvironment and completely abrogated immunosuppressive checkpoint markers TIGIT, TIM3, and CTLA-4, but not PD-1 on tumor infiltrating CD8

Indexed as

Head and Neck NeoplasmsMacrophage Migration-Inhibitory FactorsSquamous Cell Carcinoma of Head and NeckTumor MicroenvironmentAnimalsCell Line, TumorCell ProliferationFemaleHumansIntramolecular OxidoreductasesMiceT-LymphocytesIntramolecular OxidoreductasesMacrophage Migration-Inhibitory FactorsMIF protein, humanCPSI-1306Head and Neck Squamous Cell CarcinomaMacrophage migration inhibitory factorTumor microenvironment

Identifiers

PMID39644862
PMCPMC11723708

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Registered trials

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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.