Evidence map›Paper›PMID 35491652›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2022

Diminished Immune Surveillance during Histologic Progression of Intraductal Papillary Mucinous Neoplasms Offers a Therapeutic Opportunity for Cancer Interception.

Sharia Hernandez, Edwin Roger Parra, Naohiro Uraoka, Ximing Tang, Yu Shen, Wei Qiao, Mei Jiang, Shanyu Zhang, Barbara Mino, Wei Lu and 14 more

Abstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. 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.

  1. Review
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  12. Modern aspects of the management of pancreatic intraductal papillary mucinous neoplasms: a narrative review.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    Review
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

24 authors.

Sharia Hernandez *Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Edwin Roger Parra *Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-9068-1636
Naohiro UraokaDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Ximing TangDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Yu ShenDepartment of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas.
Wei QiaoDepartment of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas.
Mei JiangDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Shanyu ZhangDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Barbara MinoDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Wei LuDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Renganayaki PandurenganDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Cara HaymakerDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-1317-9287
Kajsa AffolterDepartment of Pathology, University of Utah, Salt Lake City, Utah.
Courtney L ScaifeDepartment of Surgery, University of Utah, Salt Lake City, Utah.
Michele Yip-SchneiderDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0000-0001-7569-7971
C Max SchmidtDepartment of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.
Matthew A FirpoDepartment of Surgery, University of Utah, Salt Lake City, Utah.
Sean J MulvihillDepartment of Surgery, University of Utah, Salt Lake City, Utah.ORCID 0000-0002-0078-8980
Eugene J KoayDepartment of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-7675-3461
Huamin WangDepartment of Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Ignacio I WistubaDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Anirban MaitraDepartment of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.
Luisa M Solis *Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-1253-630X
Subrata Sen *Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-6884-6246

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Utah Center for Clinical and Translational ScienceUL1TR002538 · NCATS · UNIVERSITY OF UTAH · PI HESS, RACHEL, MAJERSIK, JENNIFER JUHL · 2018 to 2022
$26.0M
Project 3: Inhibiting Oxidative Phosphorylation in Pancreatic CancerP50CA221707 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KOPETZ, SCOTT, MAITRA, ANIRBAN · 2019 to 2023
$11.0M
Clinical Validation Center for Early Detection of Pancreatic CancerU01CA200468 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ANIRBAN MAITRA · 2016 to 2026
$11.0M
Circulating Biomarkers and Imaging for Early Detection of Pancreatic CancerU01CA214263 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI EUGENE J KOAY, Subrata Sen · 2018 to 2026
$7.2M
Imaging and Molecular Correlates of Progression in Cystic Neoplasms of the PancreasU01CA196403 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MAITRA, ANIRBAN · 2015 to 2020
$5.8M
Digital Nanoplasmonic Quantification of Tumor-derived Extracellular Vesicles in Plasma MicrosamplesU01CA252965 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI HU, TONY Y., LU, HUA · 2020 to 2024
$3.0M
Pancreatic Ductal Adenocarcinoma Translational Resource Center (PATReC)U24CA224020 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MAITRA, ANIRBAN, SEN, SUBRATA · 2017 to 2021
$2.8M
NCATS NIH HHS UL1 TR002538NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA221707NCI NIH HHS U01 CA196403NCI NIH HHS U01 CA200468NCI NIH HHS U01 CA214263NCI NIH HHS U01 CA252965NCI NIH HHS U24 CA224020
6 · The paper itself

Abstract

purposeIntraductal papillary mucinous neoplasms (IPMN) are bona fide precursors to pancreatic ductal adenocarcinoma (PDAC). While genomic alterations during multistep IPMN progression have been well cataloged, the accompanying changes within the tumor immune microenvironment (TIME) have not been comprehensively studied. Herein, we investigated TIME-related alterations during IPMN progression, using multiplex immunofluorescence (mIF) coupled with high-resolution image analyses. EXPERIMENTAL

designTwo sets of formalin-fixed, paraffin-embedded tissue samples from surgically resected IPMNs were analyzed. The training set of 30 samples consisted of 11 low-grade IPMN (LG-IPMN), 17 high-grade IPMN (HG-IPMN), and 2 IPMN with PDAC, while a validation set of 93 samples comprised of 55 LG-IPMN and 38 HG-IPMN. The training set was analyzed with two panels of immuno-oncology-related biomarkers, while the validation set was analyzed with a subset of markers found significantly altered in the training set.

resultsCell types indicative of enhanced immune surveillance, including cytotoxic and memory T cells, and antigen-experienced T cells and B cells, were all found at higher densities within isolated LG-IPMNs compared with HG-IPMNs. Notably, the TIME of LG-IPMNs that had progressed at the time of surgical resection (progressor LGD) resembled that of the synchronous HG-IPMNs, underscoring that attenuated immune surveillance occurs even in LG-IPMNs destined for progression.

conclusionsOur findings provide a basis for interception of cystic neoplasia to PDAC, through maintenance of sustained immune surveillance using vaccines and other prevention approaches.

Indexed as

Adenocarcinoma, MucinousCarcinoma, Pancreatic DuctalPancreatic Intraductal NeoplasmsPancreatic NeoplasmsHumansTumor Microenvironment

Identifiers

PMID35491652
PMCPMC9069801

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.