Evidence map›Paper›PMID 41776161›Full record

ArticleNature communications2026

VISTA drives pancreatic tumor progression through modulation of the tumor-associated macrophage polarity.

Suk-Kyung Shin, Gwanghun Kim, Su Min Park, Eun-Bi Seo, Sang-Kyu Ye, Gyeong Hoon Kang, Keehoon Jung, Hyun Mu Shin, Hang-Rae Kim, Dong-Sup Lee

Abstract read
In one paragraph

Article in Nature communications, 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

10 authors.

Suk-Kyung Shin *Department of Biomedical Sciences, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-2921-4814
Gwanghun Kim *Department of Biomedical Sciences, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Su Min ParkDepartment of Biomedical Sciences, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0009-0007-3499-8664
Eun-Bi SeoDepartment of Biomedical Sciences, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Sang-Kyu YeDepartment of Biomedical Sciences, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Gyeong Hoon KangDepartment of Pathology, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-2380-6675
Keehoon JungDepartment of Biomedical Sciences, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-2199-5292
Hyun Mu ShinDepartment of Biomedical Sciences, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea. hyunmu.shin@snu.ac.kr.ORCID http://orcid.org/0000-0002-4521-8391
Hang-Rae KimSamsung Precision Genome Medicine Institute, Research Institute for Future Medicine, Samsung Medical Center, Seoul, Republic of Korea. hangrae.kim@skku.edu.
Dong-Sup LeeDepartment of Biomedical Sciences, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea. dlee5522@snu.ac.kr.ORCID http://orcid.org/0000-0001-8312-2705

Funding

Korea Health Industry Development Institute (KHIDI) RS-2024-00406325National Research Foundation of Korea (NRF) RS-2024-00345658
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) remains one of the deadliest malignancies due to its highly immunosuppressive tumor microenvironment (TME), which limits effective therapeutic interventions. Here, we demonstrate that V-domain immunoglobulin suppressor of T cell activation (VISTA) plays a crucial role in orchestrating macrophage polarity within the PDAC TME. Using murine PDAC models, we show that VISTA deficiency markedly impairs tumor growth, leading to prolonged survival. Functionally, VISTA deficiency is linked to a shift in tumor-associated macrophages (TAMs) from an immunosuppressive phenotype marked by secreted phosphoprotein 1 (SPP1), to one enriched for C-X-C motif chemokine ligand 9 (CXCL9), indicative of a pro-inflammatory state. This shift is accompanied by enhanced recruitment of CXCR3⁺ CD8⁺ T cells with sustained cytotoxic potential, among which terminal exhaustion-like CD8

Indexed as

Carcinoma, Pancreatic DuctalCell Adhesion MoleculesMacrophagesPancreatic NeoplasmsTumor-Associated MacrophagesAnimalsCD8-Positive T-LymphocytesCell Line, TumorCell PolarityChemokine CXCL9Disease ProgressionFemaleHumansMiceMice, Inbred C57BLMice, KnockoutCell Adhesion MoleculesChemokine CXCL9Cxcl9 protein, mouseCxcr3 protein, mouseOsteopontinReceptors, CXCR3

Identifiers

PMID41776161
PMCPMC13194722

What Socratic holds

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LicenceCC BY
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 Socratic graph.