Evidence map›Paper›PMID 42784801›Full record

ArticleCancer immunology research2026

IFNγ-dependent tumor-cell MHC-II is restrained by MAPK signaling and associated with immunotherapy responsiveness in pancreatic ductal adenocarcinoma.

Canping Chen, Yi Zhang, Xi Li, Tugba Y Ozmen, Furkan Ozmen, Shamilene Sivagnanam, Kyle P Gribbin, Katie E Blise, Xinxing Yang, Gangmin Kim and 10 more

Abstract read
In one paragraph

Article in Cancer immunology research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

20 authors.

Canping ChenOregon Health & Science University Portland, Oregon United States.ORCID 0000-0003-4021-8592
Yi ZhangOregon Health & Science University United States.ORCID 0000-0003-3564-5848
Xi LiTongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan China.ORCID 0000-0001-9185-7728
Tugba Y OzmenOregon Health & Science University United States.ORCID 0000-0002-7861-6759
Furkan OzmenOregon Health & Science University United States.ORCID 0000-0002-1128-9458
Shamilene SivagnanamOregon Health & Science University Portland, OR United States.ORCID 0000-0001-5966-1522
Kyle P GribbinOregon Health & Science University Portland, Oregon United States.ORCID 0000-0001-8742-4620
Katie E BliseOregon Health & Science University Portland, OR United States.ORCID 0000-0002-6433-9455
Xinxing YangOregon Health & Science University Portland, Oregon United States.ORCID 0000-0002-1512-2970
Gangmin KimOregon Health & Science University United States.ORCID 0009-0007-4475-6941
Roselyn S DaiOregon Health & Science University Portland, Oregon United States.ORCID 0009-0002-2646-8982
Dove KeithOregon Health & Science University Portland, Oregon United States.ORCID 0000-0001-6104-3264
Mara H ShermanMemorial Sloan Kettering Cancer Center New York United States.ORCID 0000-0001-7826-3888
Mu-Shui DaiOregon Health & Science University Portland, OR United States.ORCID 0000-0001-9031-6962
Lisa M CoussensOregon Health & Science University Portland, OR United States.ORCID 0000-0003-2389-1865
Charles D LopezOregon Health & Science University Portland, OR United States.ORCID 0000-0002-0921-4932
Rosalie C SearsOregon Health & Science University Portland, Oregon United States.ORCID 0000-0003-1558-2413
Gordon B MillsOHSU Knight Cancer Institute Portland, OR United States.ORCID 0000-0002-0144-9614
Katelyn T ByrneOregon Health and Science University Portland, OR United States.ORCID 0000-0002-2459-9041
Zheng XiaThe University of Texas at Austin Austin, TX United States.ORCID 0000-0003-3364-8324

Funding

Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Luiz Eduardo Bertassoni · 1997 to 2026
$60.5M
An atlas of pancreatic tumorigenesis in the context of altered DNA repair occurring in high-risk individualsU01CA294548 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI BRODY, JONATHAN, FERTIG, ELANA · 2024 to 2025
$5.1M
The Cancer Proteome Atlas: an Integrated Bioinformatics Resource for Functional Cancer Proteomic DataU24CA264128 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Rehan Akbani, Han Liang · 2022 to 2026
$3.9M
Systematic Characterization and Targeting of Neomorphic Drivers in CancerU01CA281902 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Benjamin Deneen, Han Liang · 2023 to 2026
$3.5M
Validation of novel imaging and molecular tests for early detection of pancreatic cancer through risk-stratified community engagement programsU01CA278923 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Gregory A Cote, Alexander Savio Ramos Guimaraes · 2023 to 2026
$3.3M
Mechanistic maps of adaptive responses to therapeutic stress to optimize combination therapies.U01CA253472 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI KORKUT, ANIL, LIANG, HAN · 2021 to 2025
$2.6M
Characterizing phenotype-associated subpopulations from single-cell sequencing dataR01GM147365 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Zheng Xia · 2023 to 2026
$1.2M
NCI NIH HHS P30 CA069533NCI NIH HHS U01 CA253472NCI NIH HHS U01 CA278923NCI NIH HHS U01 CA281902NCI NIH HHS U01 CA294548NCI NIH HHS U24 CA264128NIGMS NIH HHS R01 GM147365
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is characterized by an immunosuppressive tumor microenvironment (TME) and poor prognosis. Although major histocompatibility complex class II (MHC-II) is typically expressed by professional antigen-presenting cells, its regulation and significance in malignant PDAC cells remain unclear. Here, we integrated single-cell RNA sequencing, spatial transcriptomics, bulk transcriptomics, multiplex immunohistochemistry, and functional studies in murine PDAC models to investigate tumor-cell MHC-II. Across human PDAC datasets, elevated tumor-cell MHC-II expression was associated with increased CD4⁺ and CD8⁺ T-cell infiltration and localization within immune-rich tumor niches. In paired biopsies from patients treated with cobimetinib, malignant cells showed increased expression of MHC-II pathway genes, suggesting therapy-induced activation of this program. In preclinical KPC models, MHC-IIhigh tumors exhibited greater T-cell infiltration, whereas MHC-IIlow tumors derived the greatest benefit from cobimetinib combined with immune checkpoint blockade. Mechanistically, direct tumor stimulation via in vitro administration of cobimetinib and recombinant interferon (IFN)-γ resulted in MHC-II induction in vitro by both MHCIIhigh and MHC-IIlow PDAC cell lines. In vivo, combined MEK inhibition and immune checkpoint blockade-controlled tumor growth, including in MHC-IIlow tumors. Deletion of the IFN-γ receptor abolished MHC-II induction and therapeutic benefit, demonstrating that this response is IFN-γ dependent. MEK inhibition enhanced downstream IFN-γ signaling and the combination was required for MHC II upregulation in vitro, indicating that MAPK activity restrains an IFN-γ-responsive MHC-II program. Collectively, these findings identify tumor-cell MHC-II as an IFN-γ-dependent, MAPK-restrained program that denotes immunotherapy sensitivity in PDAC.

Identifiers

PMID42784801
PMCPMC13682913

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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.