Evidence map›Paper›PMID 25406955›Full record

ArticlePancreas2015

Longitudinal Bioluminescence Imaging of Primary Versus Abdominal Metastatic Tumor Growth in Orthotopic Pancreatic Tumor Models in NSG Mice.

Harlan E Shannon, Melissa L Fishel, Jingwu Xie, Dongsheng Gu, Brian P McCarthy, Amanda A Riley, Anthony L Sinn, Jayne M Silver, Kacie Peterman, Mark R Kelley and 4 more

Open access · greenAbstract readComparative StudyValidation Study
In one paragraph

Article in Pancreas, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Tissue Transglutaminase Mediated Tumor-Stroma Interaction Promotes Pancreatic Cancer Progression.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
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

14 authors at 4 institutions in 1 country.

Harlan E ShannonFrom the *Section of Pediatric Hematology/Oncology, Department of Pediatrics, Herman B Wells Center for Pediatric Research; †Department of Pharmacology and Toxicology, ‡Indiana University Simon Cancer Center (IUSCC), §Department of Biochemistry and Molecular Biology; ∥Department of Radiology and Imaging Sciences, ¶In Vivo Therapeutics Core, IUSCC, and #Department of Medicine, Indiana University School of Medicine; and **The Riley Hospital for Children, Indianapolis, IN.
Melissa L Fishel
Jingwu Xie
Dongsheng Gu
Brian P McCarthy
Amanda A Riley
Anthony L Sinn
Jayne M Silver
Kacie Peterman
Mark R Kelley
Helmut Hanenberg
Murray Korc
Karen E Pollok
Paul R Territo
Riley Hospital for Children · USIndiana University School of MedicineIndiana University · USIndiana University Health · 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
Novel aspects of Epithelial-Mesenchymal Transition(EMT)in pancreatic cancerR01CA075059 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI KORC, MURRAY · 1997 to 2018
$4.3M
Regulation of immune surveillance by hedgehog signaling in tumor microenvironmentR01CA155086 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI XIE, JINGWU · 2012 to 2016
$1.6M
NCI NIH HHS R01 CA075059NCI NIH HHS R01 CA155086NCI NIH HHS R01 CA167291
6 · The paper itself

Abstract

objectivesThe purpose of the present study was to develop and validate noninvasive bioluminescence imaging methods for differentially monitoring primary and abdominal metastatic tumor growth in mouse orthotopic models of pancreatic cancer.

methodsA semiautomated maximum entropy segmentation method was implemented for the primary tumor region of interest, and a rule-based method for manually drawing a region of interest for the abdominal metastatic region was developed for monitoring tumor growth in orthotopic models of pancreatic cancer. The 2 region-of-interest methods were validated by having 2 observers independently segment Panc-1 tumors, and the results were compared with the number of mesenteric lymph node nodules and histopathologic assessment of liver metastases. The findings were extended to orthotopic tumors of the more metastatic MIA PaCa-2 and AsPC-1 cells where separate groups of animals were implanted with different numbers of cells.

resultsThe results demonstrated that the segmentation methods were highly reliable, reproducible, and robust and allowed statistically significant discrimination in the growth rates of primary and abdominal metastatic tumors of different cell lines implanted with different numbers of cells.

conclusionsThe present results demonstrate that primary tumors and abdominal metastatic foci in orthotopic pancreatic cancer models can be reliably quantified separately and noninvasively over time with bioluminescence imaging.

Indexed as

Abdominal NeoplasmsAnimalsAutomation, LaboratoryCell Line, TumorCell ProliferationFemaleHeterograftsHumansImage Processing, Computer-AssistedLiver NeoplasmsLuminescent MeasurementsLymphatic MetastasisMaleMice, Inbred NODNeoplasm MicrometastasisNeoplasms, Experimental

Identifiers

PMID25406955
PMCPMC4262664
OpenAlexW2317907175

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.