Evidence map›Paper›PMID 38398179›Full record

ReviewCancers2024

Therapeutic Potential for Sphingolipids in Inflammatory Bowel Disease and Colorectal Cancer.

Keila S Espinoza, Ashley J Snider

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 23 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

2 authors at 1 institution in 1 country.

Keila S EspinozaDepartment of Physiology, University of Arizona, Tucson, AZ 85721, USA.ORCID 0000-0001-8514-1600
Ashley J SniderSchool of Nutritional Sciences and Wellness, University of Arizona, Tucson, AZ 85721, USA.ORCID 0000-0002-1515-4171
University of Arizona · US

Funding

Role for myeloid acid ceramidase in colon inflammation and cancerR01DK132079 · NIDDK · UNIVERSITY OF ARIZONA · PI Ashley Jones Snider · 2022 to 2026
$1.6M
NIDDK NIH HHS R01 DK132079NIH HHS RO1 DK132079
6 · The paper itself

Abstract

Inflammatory bowel disease (IBD), characterized by chronic inflammation in the intestinal tract, increases the risk for the development of colorectal cancer (CRC). Sphingolipids, which have been implicated in IBD and CRC, are a class of bioactive lipids that regulate cell signaling, differentiation, apoptosis, inflammation, and survival. The balance between ceramide (Cer), the central sphingolipid involved in apoptosis and differentiation, and sphingosine-1-phosphate (S1P), a potent signaling molecule involved in proliferation and inflammation, is vital for the maintenance of normal cellular function. Altered sphingolipid metabolism has been implicated in IBD and CRC, with many studies highlighting the importance of S1P in inflammatory signaling and pro-survival pathways. A myriad of sphingolipid analogues, inhibitors, and modulators have been developed to target the sphingolipid metabolic pathway. In this review, the efficacy and therapeutic potential for modulation of sphingolipid metabolism in IBD and CRC will be discussed.

Indexed as

ceramidecolitis-associated cancercolorectal cancerinflammationinflammatory bowel diseasesphingolipidssphingosine-1-phosphate

Identifiers

PMID38398179
PMCPMC10887199
OpenAlexW4391840510

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.