Evidence map›Paper›PMID 38928187›Full record

ArticleInternational journal of molecular sciences2024

From Inflammation to Oncogenesis: Tracing Serum DCLK1 and miRNA Signatures in Chronic Liver Diseases.

Landon L Moore, Dongfeng Qu, Sripathi Sureban, Stephanie Mitchell, Kamille Pitts, Nasya Cooper, Javid Fazili, Richard Harty, Abdul Oseini, Kai Ding and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
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

12 authors.

Landon L MooreDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.ORCID 0000-0002-0594-7960
Dongfeng QuDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.ORCID 0000-0002-9200-3852
Sripathi SurebanDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Stephanie MitchellDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Kamille PittsDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.ORCID 0000-0001-8145-7456
Nasya CooperDepartment of Natural Sciences, Langston University, Langston, OK 73050, USA.ORCID 0009-0008-3158-1705
Javid FaziliDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Richard HartyDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Abdul OseiniDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.
Kai DingDepartment of Biostatistics and Epidemiology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.ORCID 0000-0001-9475-437X
Michael BronzeDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.ORCID 0000-0002-8770-0872
Courtney W HouchenDepartment of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.ORCID 0000-0003-2487-5242

Funding

VA Merit Review CSR&D 1I01CX001686-01
6 · The paper itself

Abstract

Chronic liver diseases, fibrosis, cirrhosis, and HCC are often a consequence of persistent inflammation. However, the transition mechanisms from a normal liver to fibrosis, then cirrhosis, and further to HCC are not well understood. This study focused on the role of the tumor stem cell protein doublecortin-like kinase 1 (DCLK1) in the modulation of molecular factors in fibrosis, cirrhosis, or HCC. Serum samples from patients with hepatic fibrosis, cirrhosis, and HCC were analyzed via ELISA or NextGen sequencing and were compared with control samples. Differentially expressed (DE) microRNAs (miRNA) identified from these patient sera were correlated with DCLK1 expression. We observed elevated serum DCLK1 levels in fibrosis, cirrhosis, and HCC patients; however, TGF-β levels were only elevated in fibrosis and cirrhosis. While DE miRNAs were identified for all three disease states,

Indexed as

Doublecortin-Like KinasesInflammationIntracellular Signaling Peptides and ProteinsLiver CirrhosisLiver NeoplasmsMicroRNAsProtein Serine-Threonine KinasesAgedBiomarkers, TumorCarcinogenesisCarcinoma, HepatocellularChronic DiseaseFemaleHumansLiver DiseasesMaleBiomarkers, TumorDCLK1 protein, humanDoublecortin-Like KinasesIntracellular Signaling Peptides and ProteinsMicroRNAsProtein Serine-Threonine KinasescirrhosisDCLK1hepatocellular carcinomaliver fibrosismicroRNA

Identifiers

PMID38928187
PMCPMC11203803

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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.