Evidence map›Paper›PMID 30111533›Full record

ArticleCancer research2018

Macrophage-Derived Neuropilin-2 Exhibits Novel Tumor-Promoting Functions.

Sohini Roy, Arup K Bag, Samikshan Dutta, Navatha Shree Polavaram, Ridwan Islam, Samuel Schellenburg, Jasjit Banwait, Chittibabu Guda, Sophia Ran, Michael A Hollingsworth and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% of its field
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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. The Significance of Neuropilins in Gastrointestinal Cancers.International journal of molecular sciences · 2025
    Review
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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

15 authors at 5 institutions in 2 countries.

Sohini RoyDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska.
Arup K BagDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska.
Samikshan DuttaDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska.
Navatha Shree PolavaramDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska.
Ridwan IslamDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska.
Samuel SchellenburgInstitute of Pathology, University Hospital Carl Gustav Carus, University of Technology, Dresden, Germany.
Jasjit BanwaitDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska.
Chittibabu GudaDepartment of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, Nebraska.
Sophia RanDepartment of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine, Springfield, Illinois.
Michael A HollingsworthDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska.
Rakesh K SinghDepartment of Microbiology and Pathology, University of Nebraska Medical Center, Omaha, Nebraska.
James E TalmadgeDepartment of Microbiology and Pathology, University of Nebraska Medical Center, Omaha, Nebraska.ORCID 0000-0002-6328-6056
Michael H MudersInstitute of Pathology, University Hospital Carl Gustav Carus, University of Technology, Dresden, Germany. kaustubh.datta@unmc.edu michael.muders@ukbonn.de.
Surinder K BatraDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska.
Kaustubh DattaDepartment of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska. kaustubh.datta@unmc.edu michael.muders@ukbonn.de.
University of Nebraska Medical Center · USNebraska Medical Center · USSouthern Illinois University School of Medicine · USUniversity Hospital Carl Gustav Carus · DEUniversity of Bonn · DE

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Apar Kishor Ganti · 1985 to 2026
$55.0M
Tissue CoreP50CA127297 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLLINGSWORTH, MICHAEL A. · 2008 to 2018
$17.1M
Research Pilot Project ProgramP30GM106397 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI JOHNSON, KEITH R · 2013 to 2017
$4.9M
Role of N-Cadherin in Pancreatic Tumor MicroenvironmentU54CA163120 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BATRA, SURINDER K. · 2011 to 2015
$4.2M
Neuropilin-2 Axis in Docetaxel Resistance and Prostate Cancer Bone MetastasisR01CA182435 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DATTA, KAUSTUBH · 2015 to 2019
$1.7M
Novel role of myeloid-derived lymphatic progenitors in induction of breast cancer lymphaticsR01CA199649 · NCI · SOUTHERN ILLINOIS UNIVERSITY SCH OF MED · PI RAN, SOPHIA · 2016 to 2020
$1.7M
The role of VEGF-C in resisting stress in prostate cancerR01CA140432 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DATTA, KAUSTUBH · 2010 to 2014
$1.5M
NCI NIH HHS P30 CA036727NCI NIH HHS P50 CA127297NCI NIH HHS R01 CA140432NCI NIH HHS R01 CA182435NCI NIH HHS R01 CA199649NCI NIH HHS U54 CA163120NIGMS NIH HHS P30 GM106397
6 · The paper itself

Abstract

Tumor-associated macrophages (TAM) are causally associated with tumorigenesis as well as regulation of antitumor immune responses and have emerged as potential immunotherapeutic targets. Recent evidence suggests TAM phagocytose apoptotic tumor cells within the tumor microenvironment through efferocytosis in an immunologically silent manner, thus maintaining an immunosuppressed microenvironment. The signal transduction pathways coupling efferocytosis and immunosuppression are not well known. Neuropilin-2 (NRP2) is a member of the membrane-associated neuropilin family and has been reported in different immune cells but is poorly characterized. In this study, we show that NRP2 is expressed during macrophage differentiation, is induced by tumor cells, and regulates phagocytosis in macrophages. Furthermore, NRP2 in TAM promoted efferocytosis and facilitated tumor growth. Deletion of NRP2 from TAM impaired the clearance of apoptotic tumor cells and increased secondary necrosis within tumors. This resulted in a break in the immune tolerance and reinitiated antitumor immune responses, characterized by robust infiltration of CD8

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisCell Line, TumorCells, CulturedHumansImmune SystemImmunosuppression TherapyImmunotherapyJurkat CellsLeukocytes, MononuclearMacrophagesMiceMice, Inbred C57BLMonocytesNeoplasmsNeuropilin-2neuropilin-2, human

Identifiers

PMID30111533
PMCPMC6168405
OpenAlexW2885789377

What OpenQuestion holds

Textmetadata
LicenceTDM
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.