Evidence map›Paper›PMID 41283988›Full record

ArticleCancer research communications2025

Dipeptidyl Peptidase 4 Restoration Facilitates Antitumor Immunity in KRAS-LKB1-Mutant Lung Cancer.

Toshiyuki Tenma, Ryohei Yoshida, Hiraku Yanada, Kiichi Nitanai, Toshihiro Nagato, Kyohei Oyama, Nobunari Sasaki, Mizuki Homme, Chie Mori, Takayuki Ohkuri and 8 more

Abstract read
In one paragraph

Article in Cancer research communications, 2025. 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

18 authors.

Toshiyuki TenmaDivision of Respiratory Medicine and Neurology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.ORCID 0009-0003-1209-661X
Ryohei YoshidaDivision of Respiratory Medicine and Neurology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0002-2959-9972
Hiraku YanadaDivision of Respiratory Medicine and Neurology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.ORCID 0009-0009-9915-554X
Kiichi NitanaiDivision of Respiratory Medicine and Neurology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.ORCID 0009-0004-8653-7593
Toshihiro NagatoDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0001-8326-8296
Kyohei OyamaDepartment of Cardiac Surgery, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0002-8478-4417
Nobunari SasakiProject for Cancer Immunotherapy Development, Cancer Precision Medicine Center, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID 0009-0009-4336-588X
Mizuki HommeProject for Cancer Immunotherapy Development, Cancer Precision Medicine Center, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID 0009-0006-1747-4028
Chie MoriDivision of Respiratory Medicine and Neurology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0002-4398-1086
Takayuki OhkuriDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0002-6889-7809
Yusuke OnoInstitute of Biomedical Research, Sapporo Higashi Tokushukai Hospital, Sapporo, Japan.ORCID 0000-0001-8385-5386
Shoichiro TangeDepartment of Medical Genome Sciences, Cancer Research Institute, Sapporo Medical University School of Medicine, Sapporo, Japan.ORCID 0000-0002-2126-6938
Yoshinori MinamiDivision of Respiratory Medicine and Neurology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0002-5368-0527
Hiroya KobayashiDepartment of Pathology, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0001-5222-8961
Yusuke MizukamiInstitute of Biomedical Research, Sapporo Higashi Tokushukai Hospital, Sapporo, Japan.ORCID 0000-0002-1068-7024
David A BarbieDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID 0000-0002-5422-4275
Shunsuke KitajimaProject for Cancer Immunotherapy Development, Cancer Precision Medicine Center, Japanese Foundation for Cancer Research, Tokyo, Japan.ORCID 0000-0001-6532-2543
Takaaki SasakiDivision of Respiratory Medicine and Neurology, Department of Internal Medicine, Asahikawa Medical University, Asahikawa, Japan.ORCID 0000-0002-6505-8786

Funding

Japan Agency for Medical Research and Development (AMED) 23ama221424h0001/24ama221424h0002Kobayashi Foundation for Cancer ResearchTakeda Science Foundation (TSF)
6 · The paper itself

Abstract

KRAS proto-oncogene, GTPase (KRAS)-liver kinase B1 (LKB1)-mutant (KL) non-small cell lung cancer (NSCLC), characterized by a profoundly immunosuppressive tumor microenvironment (TME), is highly resistant to immune checkpoint inhibitors. Despite their high tumor mutation burden, KL tumors exhibit low expression of PD-L1, reduced immune cell infiltration, and suppressed immune signaling pathways. Systematic genome analyses revealed that LKB1 loss suppresses dipeptidyl peptidase 4 (DPP4) expression and activity in KRAS-mutant lung cancer. The therapeutic potential of restoring DPP4 function to improve the immune response in KL lung cancer was evaluated using patient-derived tumor samples and syngeneic mouse models. Restoration of DPP4 expression reprogrammed the TME and significantly increased immune-related gene signatures, including those involved in T-cell migration and NK-cell activation. Restoration of DPP4 expression in three-dimensional microfluidic models enhanced NK-cell chemotaxis and spheroid-targeting activity. Furthermore, DPP4 restoration was synergized with anti-PD-1 therapy to achieve significant tumor regression in syngeneic KL murine models. These findings suggest that LKB1 loss suppresses DPP4 expression, contributing to the immunosuppressive characteristics of the TME in KL-NSCLC cells, whereas restoring DPP4 expression promotes NK-cell recruitment, facilitates immune activation, and enhances the effects of anti-PD-1 therapy. These results suggest that DPP4 is a key immune modulator and a promising therapeutic target, providing a novel strategy to overcome immune resistance and improve immunotherapy outcomes in this challenging subset of lung cancer. SIGNIFICANCE: LKB1 loss suppresses DPP4 expression in KL-NSCLC; however, restoring DPP4 expression in vitro promotes NK-cell recruitment, mitigating the immunosuppressive TME and enhancing the efficacy of anti-PD-1 therapy in KL models.

Indexed as

Carcinoma, Non-Small-Cell LungDipeptidyl Peptidase 4Lung NeoplasmsProtein Serine-Threonine KinasesProto-Oncogene Proteins p21(ras)AMP-Activated Protein Kinase KinasesAnimalsCell Line, TumorHumansImmune Checkpoint InhibitorsKiller Cells, NaturalMiceMutationTumor MicroenvironmentAMP-Activated Protein Kinase KinasesDipeptidyl Peptidase 4DPP4 protein, humanImmune Checkpoint InhibitorsKRAS protein, humanProtein Serine-Threonine KinasesProto-Oncogene Proteins p21(ras)STK11 protein, human

Identifiers

PMID41283988
PMCPMC12709056

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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.