Evidence map›Paper›PMID 26437221›Full record

ArticleOncotarget2015

Induction of KIAA1199/CEMIP is associated with colon cancer phenotype and poor patient survival.

Stephen P Fink, Lois L Myeroff, Revital Kariv, Petra Platzer, Baozhong Xin, Debra Mikkola, Earl Lawrence, Nathan Morris, Arman Nosrati, James K V Willson and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

41 citing papers in PubMed, 78 citations in OpenAlex.

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  13. International journal of medical sciences · 2022
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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 2 institutions in 1 country.

Stephen P FinkDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Lois L MyeroffDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Revital KarivDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Petra PlatzerDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Baozhong XinDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Debra MikkolaDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Earl LawrenceDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Nathan MorrisDepartment of Epidemiology and Biostatistics, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Arman NosratiDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
James K V WillsonSimmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Joseph WillisDepartment of Pathology, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Martina VeiglDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Jill S Barnholtz-SloanCase Comprehensive Cancer Center, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Zhenghe WangDepartment of Genetics and Genome Sciences, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Sanford D MarkowitzDepartment of Medicine, Case Western Reserve University and Case Medical Center, Cleveland, OH, USA.
Case Western Reserve University · USThe University of Texas Southwestern Medical Center · US

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARK R CHANCE · 1987 to 2026
$142.3M
Targeting 15-PGDH in Colon Cancer Prognosis, Prediction, Treatment and PreventionP50CA150964 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARKOWITZ, SANFORD D. · 2011 to 2022
$24.6M
The Cleveland Digestive Diseases Research Core Center (DDRCC)P30DK097948 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI Theresa Torres Pizarro · 2015 to 2026
$15.6M
GENE EXPRESSION OF COLON CANCERS THAT METASTASIZEU01CA088130 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARKOWITZ, SANFORD D · 2000 to 2004
$6.7M
Identify and validate novel epigenetic molecular markers for colorectal neoplasmU01CA152756 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GRADY, WILLIAM MALLORY, GUDA, KISHORE · 2010 to 2021
$6.7M
Mechanisms of suppression of colon cancer by receptor tyrosine phosphatase PTPRTR01CA127590 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI WANG, ZHENGHE · 2007 to 2017
$2.9M
NCI NIH HHS P30 CA043703NCI NIH HHS P30CA43703NCI NIH HHS P50 CA150964NCI NIH HHS P50CA150964NCI NIH HHS R01 CA127590NCI NIH HHS U01 CA152756NCI NIH HHS U01CA88130NCI NIH HHS UO1CA152756NIDDK NIH HHS P30 DK097948
6 · The paper itself

Abstract

Genes induced in colon cancer provide novel candidate biomarkers of tumor phenotype and aggressiveness. We originally identified KIAA1199 (now officially called CEMIP) as a transcript highly induced in colon cancer: initially designating the transcript as Colon Cancer Secreted Protein 1. We molecularly characterized CEMIP expression both at the mRNA and protein level and found it is a secreted protein induced an average of 54-fold in colon cancer. Knockout of CEMIPreduced the ability of human colon cancer cells to form xenograft tumors in athymic mice. Tumors that did grow had increased deposition of hyaluronan, linking CEMIP participation in hyaluronan degradation to the modulation of tumor phenotype. We find CEMIP mRNA overexpression correlates with poorer patient survival. In stage III only (n = 31) or in combined stage II plus stage III colon cancer cases (n = 73), 5-year overall survival was significantly better (p = 0.004 and p = 0.0003, respectively) among patients with low CEMIP expressing tumors than those with high CEMIP expressing tumors. These results demonstrate that CEMIP directly facilitates colon tumor growth, and high CEMIP expression correlates with poor outcome in stage III and in stages II+III combined cohorts. We present CEMIP as a candidate prognostic marker for colon cancer and a potential therapeutic target.

Indexed as

AnimalsBiomarkers, TumorCell Line, TumorCell ProliferationColonColonic NeoplasmsFemaleGene Expression Regulation, NeoplasticGene Knockout TechniquesHeLa CellsHumansHyaluronic AcidHyaluronoglucosaminidaseIntestinal MucosaKaplan-Meier EstimateMiceBiomarkers, TumorCEMIP protein, humanHyaluronic AcidHyaluronoglucosaminidaseProteinsRNA, MessengerCEMIPcolon cancermetastasisprognostic markersecreted protein

Identifiers

PMID26437221
PMCPMC4741547
OpenAlexW2179344918

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.