Evidence map›Paper›PMID 41312741›Full record

ReviewMolecular medicine reports2026

Liver X receptor: A potential target for inflammatory bowel disease and colorectal cancer (Review).

Yingjie Li, Xiaoyan Fu, Meiwen Bai, Jiaqi Zhou, Jiatai Qiu, Hongxia Zhang, Shujuan Liang, Meifang Liu

Abstract readReview
In one paragraph

Review in Molecular medicine reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Yingjie Li *Lab for Immune Microenvironment and Inflammatory Disease Research in Universities of Shandong Province, School of Basic Medical Sciences, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.
Xiaoyan Fu *Lab for Immune Microenvironment and Inflammatory Disease Research in Universities of Shandong Province, School of Basic Medical Sciences, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.
Meiwen Bai *Lab for Immune Microenvironment and Inflammatory Disease Research in Universities of Shandong Province, School of Basic Medical Sciences, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.
Jiaqi ZhouLab for Immune Microenvironment and Inflammatory Disease Research in Universities of Shandong Province, School of Basic Medical Sciences, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.
Jiatai QiuLab for Immune Microenvironment and Inflammatory Disease Research in Universities of Shandong Province, School of Basic Medical Sciences, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.
Hongxia ZhangLab for Immune Microenvironment and Inflammatory Disease Research in Universities of Shandong Province, School of Basic Medical Sciences, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.
Shujuan LiangLab for Immune Microenvironment and Inflammatory Disease Research in Universities of Shandong Province, School of Basic Medical Sciences, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.
Meifang LiuLab for Immune Microenvironment and Inflammatory Disease Research in Universities of Shandong Province, School of Basic Medical Sciences, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver X receptor (LXR), comprising isoforms LXRα and LXRβ, is a member of the nuclear receptor family, which serves important roles in maintaining cholesterol and lipid metabolism homeostasis by regulating cholesterol excretion and reverse transport. LXR activation also participates in regulating the pathological processes of inflammation and tumor‑related processes, such as proliferation and apoptosis. Inflammatory bowel disease (IBD) and colorectal cancer (CRC) are two common intestinal inflammatory diseases, and the occurrence of CRC is closely associated with the development of chronic inflammation, particularly IBD. To date, the pathogenesis of IBD and CRC remains to be fully elucidated, although research is being conducted in this area. LXR has been suggested to participate in regulating the pathogenesis of both IBD and CRC. Although previous findings illustrate the benefits of LXR activation on intestinal inflammatory response and cancer, there remains a lack of comprehensive understanding of how LXR exerts its properties. The present review provided an overview of the recent advances in understanding the roles of LXR in IBD and CRC, to explore the potential therapeutic strategies and targets mediated by the dual roles of LXR in immune modulation and cholesterol metabolism, and to identify the link between IBD and CRC. The present review highlighted the novel role of LXR in bridging metabolic regulation and immune homeostasis, positioning it as a promising therapeutic target for IBD and CRC.

Indexed as

Colorectal NeoplasmsInflammatory Bowel DiseasesLiver X ReceptorsAnimalsCholesterolHumansLipid MetabolismCholesterolLiver X Receptorscolorectal cancerinflammationinflammatory bowel diseaseintestinalliver X receptor

Identifiers

PMID41312741
PMCPMC12690516

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.