Evidence map›Paper›PMID 31533087›Full record

ArticleAging2019

Up-regulation of lysophosphatidylcholine acyltransferase 1 (LPCAT1) is linked to poor prognosis in breast cancer.

Patrick Lebok, Aurelia von Hassel, Jan Meiners, Claudia Hube-Magg, Ronald Simon, Doris Höflmayer, Andrea Hinsch, David Dum, Christoph Fraune, Cosima Göbel and 19 more

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

29 citing papers in PubMed, 49 citations in OpenAlex.

  1. Association ofBiomedicines · 2025
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  13. Microbiome and Prostate Cancer: A Novel Target for Prevention and Treatment.International journal of molecular sciences · 2023
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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

29 authors at 7 institutions in 2 countries.

Patrick LebokDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Aurelia von HasselDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Jan MeinersGeneral, Visceral and Thoracic Surgery Department and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Claudia Hube-MaggDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Ronald SimonDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Doris HöflmayerDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Andrea HinschDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
David DumDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Christoph FrauneDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Cosima GöbelDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Katharina MöllerDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Guido SauterDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Frank JacobsenDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Franziska BüscheckDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Kristina PrienDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Till KrechDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Rainer Horst KrechDepartment of Pathology, Clinical Center Osnabrück, Osnabrück D-49076, Germany.
Albert von der AssenBreast cancer center, Niels-Stensen Clinic, Franziskus-Hospital Harderberg, Georgsmarienhütte D-49124, Germany.
Linn WölberDepartment of Gynecology and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Isabell WitzelDepartment of Gynecology and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Barbara SchmalfeldtDepartment of Gynecology and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Stefan GeistDepartment of Gynecology, Regio Clinic Pinneberg, Pinneberg D-25421, Germany.
Peter PaluchoswskiDepartment of Gynecology, Regio Clinic Pinneberg, Pinneberg D-25421, Germany.
Christian WilkeDepartment of Gynecology, Regio Clinic Elmshorn, Elmshorn D-25337, Germany.
Uwe HeilenkötterDepartment of Gynecology, Regio Clinic and Senior Citizen Center Itzehoe, Itzehoe D-25524, Germany.
Luigi TerraccianoCantonal Hospital Basel, University of Basel, Basel CH-4031, Switzerland.
Volkmar MüllerDepartment of Gynecology and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Waldemar WilczakDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
Eike Christian BurandtDepartment of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg D-20246, Germany.
University Medical Center Hamburg-Eppendorf · DEUniversität Hamburg · DERegio Kliniken · DEKlinikum Itzehoe · DEOsnabrück University · DESt. Franziskus Hospital · DEUniversity Hospital of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of lipid metabolism is common in cancer. Lysophosphatidylcholine acyltransferase 1 (LPCAT1) has been implicated with various cancer types. Here we analyzed by immunohistochemistry its expression in 2,197 breast cancers. LPCAT1 staining was found in 97.8% of 1,774 interpretable tumors, including 48.1% with weak, 28.7% with moderate, and 14.4% with strong expression. The frequency of LPCAT1 positivity depended on the histological tumor type. Moderate or strong LPCAT1 positivity was more common in cancers of no special type (NST) (46.2%) than in lobular carcinomas (25.9%; p<0.0001). Strong LPCAT1 was associated with BRE grade, tumor cell proliferation and overall survival in all cancers and in the subgroup of NST cancers (p<0.0001, each). In the subset of NST cancers the prognostic effect of LPCAT1 expression was independent of pT, and BRE grade (p<0.0001 each). A comparison with molecular features showed that LPCAT1 was strongly associated with estrogen receptor negativity (p<0.0001), progesterone receptor negativity (p<0,0001), amplification of HER2 (p<0.0001) and MYC (p=0.0066), as well as deletions of PTEN (p<0.0001) and CDKNA2 (p=0.0151). It is concluded that LPCAT1 overexpression is linked to adverse tumor features and poor prognosis in breast cancer. These data also highlight the important role of lipid metabolism in breast cancer biology.

Indexed as

Gene Expression Regulation, NeoplasticUp-Regulation1-Acylglycerophosphocholine O-AcyltransferaseAdultAgedAged, 80 and overBreastBreast NeoplasmsCarcinomaCell ProliferationFemaleHumansMiddle AgedPrognosisSurvival Rate1-Acylglycerophosphocholine O-AcyltransferaseLpcat1 protein, humanbreast cancerimmunohistochemistryLPCAT1prognosisTMA

Identifiers

PMID31533087
PMCPMC6781992
OpenAlexW2978104935

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.