Evidence map›Paper›PMID 23633481›Full record

ArticleCancer research2013

Dynamic mast cell-stromal cell interactions promote growth of pancreatic cancer.

Ying Ma, Rosa F Hwang, Craig D Logsdon, Stephen E Ullrich

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed, 1 pooled it
7.0field-weighted citation impact, top 2% 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

128 citing papers in PubMed, 1 synthesis or guideline pooled it, 195 citations in OpenAlex.

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  20. Cold and hot tumors: from molecular mechanisms to targeted therapy.Signal transduction and targeted therapy · 2024
    Review

68 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Ying MaDepartment of Immunology and the Center for Cancer Immunology Research, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.
Rosa F Hwang
Craig D Logsdon
Stephen E Ullrich
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
Alcohol Induced Chronic PancreatitisR01AA020822 · NIAAA · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LOGSDON, CRAIG D · 2012 to 2016
$1.7M
Does UV-induced Unconventional Mast Cell Migration Activate Immune Suppression?R01CA131207 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ULLRICH, STEPHEN E · 2008 to 2012
$1.6M
NCI NIH HHS CA131207NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA131207NIAAA NIH HHS R01 AA020822
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) exists in a complex desmoplastic microenvironment, which includes cancer-associated fibroblasts [also known as pancreatic stellate cells (PSC)] and immune cells that provide a fibrotic niche that impedes successful cancer therapy. We have found that mast cells are essential for PDAC tumorigenesis. Whether mast cells contribute to the growth of PDAC and/or PSCs is unknown. Here, we tested the hypothesis that mast cells contribute to the growth of PSCs and tumor cells, thus contributing to PDAC development. Tumor cells promoted mast cell migration. Both tumor cells and PSCs stimulated mast cell activation. Conversely, mast cell-derived interleukin (IL)-13 and tryptase stimulated PSC proliferation. Treating tumor-bearing mice with agents that block mast cell migration and function depressed PDAC growth. Our findings suggest that mast cells exacerbate the cellular and extracellular dynamics of the tumor microenvironment found in PDAC. Therefore, targeting mast cells may inhibit stromal formation and improve therapy.

Indexed as

Cell ProliferationAnimalsAntineoplastic AgentsBenzylaminesCarcinoma, Pancreatic DuctalCell CommunicationCell DegranulationCell Line, TumorCell MovementCoculture TechniquesCulture Media, ConditionedCyclamsEpithelial CellsHeterocyclic CompoundsHumansInterleukin-13Antineoplastic AgentsBenzylaminesCulture Media, ConditionedCyclamsHeterocyclic CompoundsInterleukin-13plerixaforReceptors, CXCR4Tryptases

Identifiers

PMID23633481
PMCPMC3702652
OpenAlexW2126868151

What OpenQuestion holds

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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.