Evidence map›Paper›PMID 32238357›Full record

ArticleCancer research2020

Long-Term Gemcitabine Treatment Reshapes the Pancreatic Tumor Microenvironment and Sensitizes Murine Carcinoma to Combination Immunotherapy.

Daniel R Principe, Matthew Narbutis, Sandeep Kumar, Alex Park, Navin Viswakarma, Matthew J Dorman, Suneel D Kamath, Paul J Grippo, Melissa L Fishel, Rosa F Hwang and 5 more

Open access · greenAbstract readComment
In one paragraph

Article in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
7.4field-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

76 citing papers in PubMed, 121 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 1 country.

Daniel R PrincipeMedical Scientist Training Program, University of Illinois College of Medicine, Chicago, Illinois. arana@uic.edu principe@illinois.edu.
Matthew NarbutisDepartment of Surgery, University of Illinois at Chicago, Chicago, Illinois.
Sandeep KumarDepartment of Surgery, University of Illinois at Chicago, Chicago, Illinois.
Alex ParkUniversity of Illinois College of Medicine, Chicago, Illinois.ORCID 0000-0002-2346-5949
Navin ViswakarmaDepartment of Surgery, University of Illinois at Chicago, Chicago, Illinois.
Matthew J DormanDepartment of Surgery, University of Illinois at Chicago, Chicago, Illinois.
Suneel D KamathFeinberg School of Medicine, Northwestern University, Chicago, Illinois.ORCID 0000-0003-0117-366X
Paul J GrippoDepartment of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Melissa L FishelDepartment of Pediatrics, Indiana University School of Medicine, Indiana University, Indianapolis, Indiana.
Rosa F HwangDepartment of Breast Surgical Oncology, Division of Surgery, MD Anderson Cancer Center, University of Texas, Houston, Texas.ORCID 0000-0002-3103-6511
Dinesh ThummuriDepartment of Pharmacodynamics, College of Pharmacy, University of Florida, Gainesville, Florida.
Patrick W UnderwoodDepartment of Surgery, University of Florida College of Medicine, Gainesville, Florida.ORCID 0000-0002-8267-8979
Hidayatullah G MunshiFeinberg School of Medicine, Northwestern University, Chicago, Illinois.ORCID 0000-0002-9552-0775
Jose G TrevinoDepartment of Surgery, University of Florida College of Medicine, Gainesville, Florida.
Ajay RanaDepartment of Surgery, University of Illinois at Chicago, Chicago, Illinois. arana@uic.edu principe@illinois.edu.ORCID 0000-0003-0951-2566
University of Illinois Chicago · USIllinois College · USNorthwestern University · USUniversity of Florida · USAmerican Association of Colleges of Pharmacy · USIndiana University – Purdue University Indianapolis · USThe University of Texas MD Anderson Cancer Center · US

Funding

Novel Role of Ref-1 in Pancreatic Cancer Etiology and ProgressionR01CA167291 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI FISHEL, MELISSA L., KELLEY, MARK R. · 2013 to 2022
$5.2M
Developing Nano Technology for HER2 Directed TherapyR01CA216410 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LI, SONG, RANA, AJAY NMN · 2017 to 2021
$2.8M
Galpha13 and pancreatic cancer progressionR01CA217907 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MUNSHI, HIDAYATULLAH G. · 2018 to 2022
$1.8M
Targeting BET Bromodomain in Pancreatic CancerR01CA186885 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MUNSHI, HIDAYATULLAH G. · 2014 to 2017
$1.4M
Augmenting Pancreatic Cancer Immunotherapy via TGFβ Pathway InhibitionF30CA236031 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PRINCIPE, DANIEL R · 2019 to 2023
$256k
BLR&D Research Career Scientist Award ApplicationIK6BX004855 · VA · JESSE BROWN VA MEDICAL CENTER · PI AJAY NMN RANA · 2020 to 2026
–
Targeting MNK Pathways in Pancreatic CancerI01BX002922 · VA · JESSE BROWN VA MEDICAL CENTER · PI MUNSHI, HIDAYATULLAH G. · 2017 to 2020
–
Targeting Mixed Lineage Kinase3-Hedgehog Axis in Pancreatic CancerI01BX002703 · VA · JESSE BROWN VA MEDICAL CENTER · PI RANA, AJAY NMN · 2015 to 2019
–
BLRD VA I01 BX002703BLRD VA I01 BX002922BLRD VA I01 BX004903BLRD VA IK6 BX004855NCI NIH HHS F30 CA236031NCI NIH HHS R01 CA167291NCI NIH HHS R01 CA186885NCI NIH HHS R01 CA216410NCI NIH HHS R01 CA217907
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is a leading cause of cancer-related death with a median survival time of 6-12 months. Most patients present with disseminated disease and the majority are offered palliative chemotherapy. With no approved treatment modalities for patients who progress on chemotherapy, we explored the effects of long-term gemcitabine administration on the tumor microenvironment to identify potential therapeutic options for chemorefractory PDAC. Using a combination of mouse models, primary cell line-derived xenografts, and established tumor cell lines, we first evaluated chemotherapy-induced alterations in the tumor secretome and immune surface proteins by high throughput proteomic arrays. In addition to enhancing antigen presentation and immune checkpoint expression, gemcitabine consistently increased the synthesis of CCL/CXCL chemokines and TGFβ-associated signals. These secreted factors altered the composition of the tumor stroma, conferring gemcitabine resistance to cancer-associated fibroblasts

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsAnimalsCell Line, TumorDeoxycytidineGemcitabineHumansImmunotherapyMiceProteomicsTumor MicroenvironmentDeoxycytidineGemcitabine

Identifiers

PMID32238357
PMCPMC7777391
OpenAlexW3014605876

What OpenQuestion holds

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Registered trials

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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.