Evidence map›Paper›PMID 32918133›Full record

ArticleSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2021

FIBCD1 ameliorates weight loss in chemotherapy-induced murine mucositis.

Maria C E Andersen, Malene W Johansen, Thomas Nissen, Anders B Nexoe, Gunvor I Madsen, Grith L Sorensen, Uffe Holmskov, Anders Schlosser, Jesper B Moeller, Steffen Husby and 1 more

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In one paragraph

Article in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

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  7. Nutrition support use and clinical outcomes in patients with multiple myeloma undergoing autologous stem cell transplant.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 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

11 authors at 2 institutions in 1 country.

Maria C E AndersenHans Christian Andersen Children's Hospital, Odense University Hospital, Sdr. Boulevard 29, DK-5000, Odense C, Denmark.
Malene W JohansenHans Christian Andersen Children's Hospital, Odense University Hospital, Sdr. Boulevard 29, DK-5000, Odense C, Denmark.
Thomas NissenDepartment of Cancer and Inflammation Research, University of Southern Denmark, Odense, Denmark.
Anders B NexoeDepartment of Cancer and Inflammation Research, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0003-1674-9748
Gunvor I MadsenDepartment of Pathology, Odense University Hospital, Odense, Denmark.
Grith L SorensenDepartment of Cancer and Inflammation Research, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0002-5273-1097
Uffe HolmskovDepartment of Cancer and Inflammation Research, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0002-2391-9445
Anders SchlosserDepartment of Cancer and Inflammation Research, University of Southern Denmark, Odense, Denmark.
Jesper B MoellerDepartment of Cancer and Inflammation Research, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0001-8786-8037
Steffen HusbyHans Christian Andersen Children's Hospital, Odense University Hospital, Sdr. Boulevard 29, DK-5000, Odense C, Denmark.ORCID https://orcid.org/0000-0002-6286-2496
Mathias RatheHans Christian Andersen Children's Hospital, Odense University Hospital, Sdr. Boulevard 29, DK-5000, Odense C, Denmark. mathias.rathe@rsyd.dk.ORCID https://orcid.org/0000-0002-7533-3112
University of Southern Denmark · DKOdense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeChemotherapy-induced gastrointestinal toxicity is a common adverse event during chemotherapeutic treatment. No uniformly applicable strategies exist to predict, prevent, or treat gastrointestinal toxicity. Thus, a goal of mucositis research is to identify targets for therapeutic interventions and individualized risk prediction. Fibrinogen C domain containing 1 (FIBCD1) is a transmembrane protein expressed in human intestinal epithelial cells with functions in the innate immune system. Previous observations have shown that FIBCD1 ameliorates dextran sulfate sodium (DSS)-induced intestinal inflammation in vivo. We evaluated the effect of FIBCD1 in a murine model of chemotherapy-induced gastrointestinal toxicity and inflammation.

methodsTransgenic (Tg) mice overexpressing FIBCD1 in the intestinal epithelium (Fibcd1

resultsFollowing doxorubicin treatment, WT mice exhibited an increased weight loss compared with Tg littermates (p < 0.001). No differences between genotypes were seen in mucositis score, intestinal length, villus height/crypt depth, or IL-6, IL-1β, and Tnfα expression.

conclusionOur findings suggest that FIBCD1 could ameliorate chemotherapy-induced gastrointestinal toxicity by reducing weight loss; however, the mechanism of this possible protective effect remains to be defined warranting additional investigations.

Indexed as

Antineoplastic AgentsMucositisReceptors, Cell SurfaceWeight LossAnimalsDisease Models, AnimalGenotypeInjections, IntraperitonealMaleMiceMice, Inbred C57BLAntineoplastic AgentsFIBCD1 protein, humanReceptors, Cell SurfaceChemotherapyDoxorubicinFibrinogen C domain containing 1Gastrointestinal toxicityInnate ImmunityMucositis

Identifiers

PMID32918133
OpenAlexW3085411174

What OpenQuestion holds

Textmetadata
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.