Evidence map›Paper›PMID 15748292›Full record

ArticleBMC gastroenterology2005

Elevated creatine kinase activity in primary hepatocellular carcinoma.

Georg Meffert, Frank N Gellerich, Raimund Margreiter, Markus Wyss

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

22 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Elevated Creatine Kinase as a Marker for Aggressive GI Malignancy.Journal of community hospital internal medicine perspectives · 2025
    Article
  4. Article
  5. Article
  6. Metabolic reservoir cycles in cancer.Seminars in cancer biology · 2022
    Review
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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

4 authors at 1 institution in 1 country.

Georg MeffertDepartment of General and Transplant Surgery, University Hospital, Anichstrasse 35, A-6020 Innsbruck, Austria. GMeffert@gmx.ch <GMeffert@gmx.ch>
Frank N Gellerich
Raimund Margreiter
Markus Wyss
University Hospital Innsbruck · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInconsistent findings have been reported on the occurrence and relevance of creatine kinase (CK) isoenzymes in mammalian liver cells. Part of this confusion might be due to induction of CK expression during metabolic and energetic stress.

methodsThe specific activities and isoenzyme patterns of CK and adenylate kinase (AdK) were analysed in pathological liver tissue of patients undergoing orthotopic liver transplantation.

resultsThe brain-type, cytosolic BB-CK isoenzyme was detected in all liver specimens analysed. Conversely, CK activity was strongly increased and a mitochondrial CK (Mi-CK) isoenzyme was detected only in tissue samples of two primary hepatocellular carcinomas (HCCs).

conclusionThe findings do not support significant expression of CK in normal liver and most liver pathologies. Instead, many of the previous misconceptions in this field can be explained by interference from AdK isoenzymes. Moreover, the data suggest a possible interplay between p53 mutations, HCC, CK expression, and the growth-inhibitory effects of cyclocreatine in HCC. These results, if confirmed, could provide important hints at improved therapies and cures for HCC.

Indexed as

Adenylate KinaseAnimalsCarcinoma, HepatocellularCreatine KinaseCreatine Kinase, BB FormCreatine Kinase, Mitochondrial FormHumansLiverLiver NeoplasmsRatsAdenylate KinaseCreatine KinaseCreatine Kinase, BB FormCreatine Kinase, Mitochondrial Form

Identifiers

PMID15748292
PMCPMC555552
OpenAlexW1583184506

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.