Evidence map›Paper›PMID 26182901›Full record

ArticleDigestive diseases and sciences2015

CUEDC2 Protects Against Experimental Colitis and Suppresses Excessive Proliferation of Intestinal Mucosa.

Shaoxin Wang, Jiang Pu, Na Li, Chuanfeng Li, Chao Li, Lan Yu, Xiaohui Wang, Shanfeng Fu, Lihong Cui

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Article in Digestive diseases and sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

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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

3 citing papers in PubMed, 4 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

9 authors at 2 institutions in 1 country.

Shaoxin WangDepartment of Digestive, Navy General Hospital, Beijing, 100048, China. wangshaoxinby005@sina.com.
Jiang PuDepartment of Digestive, Navy General Hospital, Beijing, 100048, China.
Na LiDepartment of Laboratory, Navy General Hospital, Beijing, 100048, China.
Chuanfeng LiDepartment of Digestive, The Third Hospital of Peking University, Beijing, 100191, China.
Chao LiDepartment of Digestive, Navy General Hospital, Beijing, 100048, China.
Lan YuDepartment of Digestive, Navy General Hospital, Beijing, 100048, China.
Xiaohui WangDepartment of Digestive, Navy General Hospital, Beijing, 100048, China.
Shanfeng FuDepartment of Digestive, Navy General Hospital, Beijing, 100048, China.
Lihong CuiDepartment of Digestive, Navy General Hospital, Beijing, 100048, China. luckycui861@sina.com.
PLA Navy General Hospital · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCUEDC2, a CUE domain-containing protein, is highly expressed in many tumors, which also may be associated with inflammation.

aimsIn this study, we studied whether CUEDC2 plays a role in the progress of inflammatory bowel disease using CUEDC2 knockout (KO) mice and discussed the effects of CUEDC2 on cell proliferation in colonic mucosa.

methodsCUEDC2 KO mice were administered with drinking dextran sodium sulfate (DSS) to establish colitis mice model. At different time points after DSS administration, body weight and stool consistency of mice were graded. Cytokines in colon tissue such as IL-6 were measured by RT-PCR. NF-κB and STAT3 signaling pathways in colon tissue were assessed by western blotting. Besides, cell proliferation of intestinal mucosa was analyzed by immunohistochemical staining.

resultsCUEDC2 alleviated the colonic inflammation, showing elevated body weight loss, worse diarrhea, and more severe colonic mucosal injury in CUEDC2 KO mice than WT mice. Moreover, pro-inflammatory cytokines such as IL-6, TNFα, COX2, and MIP2 were significantly elevated. In CUEDC2 KO mice, the NF-κB and STAT3 signaling pathways were increasingly activated in different stages of progression of the colonic inflammation, and the percentage of proliferating cells as indicated by Ki67, CyclinD1, and BrdU in the inflammatory tissues was significantly increased.

conclusionsOur findings demonstrate that CUEDC2 plays an important role in protection from colonic inflammation, primarily by inhibiting the NF-κB and STAT3 signaling pathways and preventing excessive proliferation of the inflammatory epithelial cell.

Indexed as

AnimalsCell ProliferationColitisColonDextran SulfateEpithelial CellsGene Expression RegulationInflammationIntestinal MucosaMiceMice, KnockoutNF-kappa BRepressor ProteinsSignal TransductionSTAT3 Transcription FactorCUEDC2 protein, mouseDextran SulfateNF-kappa BRepressor ProteinsStat3 protein, mouseSTAT3 Transcription FactorCUEDC2InflammationInflammatory bowel diseaseProliferation

Identifiers

PMID26182901
OpenAlexW930893277

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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.