Evidence map›Paper›PMID 29094309›Full record

ArticleDigestive diseases and sciences2017

Increased IFRD1 Expression in Human Colon Cancers Predicts Reduced Patient Survival.

Mark A Lewis, Noura Sharabash, Zhi-Feng Miao, Lydia N Lyons, Jay Piccirillo, Donna Kallogjeri, Mario Schootman, Matthew Mutch, Yan Yan, Marc S Levin and 5 more

Open access · greenAbstract read
In one paragraph

Article in Digestive diseases and sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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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 4 institutions in 3 countries.

Mark A LewisDivision of Gastroenterology, Department of Medicine, Washington University School of Medicine, 660 South Euclid Avenue, Box 8124, St. Louis, MO, 63110, USA.
Noura SharabashDivision of Gastroenterology, Department of Medicine, Washington University School of Medicine, 660 South Euclid Avenue, Box 8124, St. Louis, MO, 63110, USA.
Zhi-Feng MiaoDivision of Gastroenterology, Department of Medicine, Washington University School of Medicine, 660 South Euclid Avenue, Box 8124, St. Louis, MO, 63110, USA.
Lydia N LyonsDivision of Gastroenterology, Department of Medicine, Washington University School of Medicine, 660 South Euclid Avenue, Box 8124, St. Louis, MO, 63110, USA.
Jay PiccirilloDepartment of Surgery, Washington University School of Medicine, 660 South Euclid Avenue, Box 8115, St. Louis, MO, 63110, USA.
Donna KallogjeriDepartment of Surgery, Washington University School of Medicine, 660 South Euclid Avenue, Box 8115, St. Louis, MO, 63110, USA.
Mario SchootmanDivision of Gastroenterology, Department of Medicine, Washington University School of Medicine, 660 South Euclid Avenue, Box 8124, St. Louis, MO, 63110, USA.
Matthew MutchDepartment of Surgery, Washington University School of Medicine, 660 South Euclid Avenue, Box 8109, St. Louis, MO, 63110, USA.
Yan YanDepartment of Surgery, Washington University School of Medicine, 660 South Euclid Avenue, Box 8100, St. Louis, MO, 63110, USA.
Marc S LevinDivision of Gastroenterology, Department of Medicine, Washington University School of Medicine, 660 South Euclid Avenue, Box 8124, St. Louis, MO, 63110, USA.
Antoni CastellsHospital Clinic de Barcelona, Barcelona, Spain.
Miriam CuatrecasasHospital Clinic de Barcelona, Barcelona, Spain.
Jason C MillsDivision of Gastroenterology, Department of Medicine, Washington University School of Medicine, 660 South Euclid Avenue, Box 8124, St. Louis, MO, 63110, USA.
Zhen-Ning WangDepartment of Surgical Oncology, First Hospital of China Medical University, No. 155 North Nanjing Street, Shenyang, Liaoning Province, China.
Deborah C RubinDivision of Gastroenterology, Department of Medicine, Washington University School of Medicine, 660 South Euclid Avenue, Box 8124, St. Louis, MO, 63110, USA. drubin@wustl.edu.ORCID 0000-0002-4192-909X
Washington University in St. Louis · USHospital Clínic de Barcelona · ESCarle Foundation Hospital · USFirst Hospital of China Medical University · CN

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
REGULATION OF ATROPHY-INDUCED PROGENITOR CELLS IN THE GASTRIC CORPUSR01DK094989 · NIDDK · WASHINGTON UNIVERSITY · PI Jason C Mills · 2012 to 2026
$6.1M
MECHANISMS OF CHIEF CELL DEDIFFERENTIATIONR01DK105129 · NIDDK · WASHINGTON UNIVERSITY · PI Jason C Mills · 2015 to 2026
$5.4M
The Role of EBI3 in Regulating Gastritis and Gastric CarcinogenesisR01DK110406 · NIDDK · SAINT LOUIS UNIVERSITY · PI DIPAOLO, RICHARD J · 2016 to 2020
$2.3M
MYOFIBROBLAST REGULATION OF THE STEM CELL NICHE IN SHORT BOWEL SYNDROMER01DK106382 · NIDDK · WASHINGTON UNIVERSITY · PI RUBIN, DEBORAH C. · 2015 to 2018
$1.4M
Bile acid metabolomics and metagenomics in short bowel syndromeR01DK112378 · NIDDK · WASHINGTON UNIVERSITY · PI DAVIDSON, NICHOLAS O., RUBIN, DEBORAH C. · 2016 to 2018
$1.1M
The Role of Inflammation in Regulating Gastritis and Gastric CarcinogenesisR56DK110406 · NIDDK · SAINT LOUIS UNIVERSITY · PI DIPAOLO, RICHARD J · 2021 to 2021
$486k
FUNCTION OF NEURONAL NOS IN KIDNEYF32DK009489 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TRAYNOR, TIMOTHY R · 1996 to 1998
–
NIDDK NIH HHS 105129NIDDK NIH HHS 110406NIDDK NIH HHS DK09489NIDDK NIH HHS DK52574NIDDK NIH HHS F32 DK009489NIDDK NIH HHS P30 DK052574NIDDK NIH HHS R01 DK094989NIDDK NIH HHS R01 DK105129NIDDK NIH HHS R01 DK106382NIDDK NIH HHS R01 DK110406NIDDK NIH HHS R01 DK112378NIDDK NIH HHS R56 DK110406
6 · The paper itself

Abstract

backgroundColon cancer (CRC) is the third most common cancer worldwide. CRC develops through combinations of genetic and epigenetic changes. However, there is marked heterogeneity in the "driver gene" mutational profiles within and among colon cancers from individual patients, and these are not sufficient to explain differences in colon cancer behavior and treatment response. Global modulation of the tumor landscape may play a role in cancer behavior. Interferon-related developmental regulator 1 (IFRD1) is a transcriptional co-regulator that modulates expression of large gene cassettes and plays a role in gut epithelial proliferation following massive intestinal resection.

aimsWe address the hypothesis that increased IFRD1 expression in colon cancers is associated with poorer patient survival.

methodsTumor and normal tissue from colon cancer patient cohorts from the USA, Spain, and China were used for this study. Cancers were scored for the intensity of IFRD1 immunostaining. The primary clinical outcome was overall survival defined as time from diagnosis to death due to cancer. Kaplan-Meier method and log-rank analysis were used to assess the association between IFRD1 expression and survival.

resultsAlmost all (98.7%) colon cancers showed readily detectable IFRD1 expression, with immunoreactivity primarily in the tumor cytoplasm. High IFRD1 colon cancer expression was significantly associated with decreased 5-year patient survival. Patients in the American cohort with high IFRD1 expression had a poorer prognosis.

conclusionsWe have demonstrated that high IFRD1 protein expression in colon cancer is associated with poorer patient prognosis, suggesting a potential role for IFRD1 in modulating tumor behavior.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overColonic NeoplasmsFemaleHumansImmediate-Early ProteinsIntestinal MucosaMaleMiddle AgedMissouriIFRD1 protein, humanImmediate-Early ProteinsHuman colon cancerIFRD1Transcriptional co-regulatorTumor landscape

Identifiers

PMID29094309
PMCPMC6167971
OpenAlexW2766317133

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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.