Evidence map›Paper›PMID 25243473›Full record

ArticlePloS one2014

Expression of mitochondrial regulators PGC1α and TFAM as putative markers of subtype and chemoresistance in epithelial ovarian carcinoma.

Marike Gabrielson, My Björklund, Joseph Carlson, Maria Shoshan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 49 citations in OpenAlex.

  1. Mitochondrial function meets oncology: the multifaceted role of TFAM across cancer types.Apoptosis : an international journal on programmed cell death · 2026
    Review
  2. Subcellular Stress Markers in Epithelial Ovarian Cancer.International journal of molecular sciences · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Article
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  9. Mitochondria transcription and cancer.Cell death discovery · 2024
    Review
  10. Article
  11. Article
  12. Article
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  15. Review
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  19. Article
  20. PGC1α and VDAC1 expression in endometrial cancer.Molecular and clinical oncology · 2021
    Article
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.

Marike GabrielsonDepartment of Oncology-Pathology, Cancer Center Karolinska CCK, Karolinska Institutet, Stockholm, Sweden.
My BjörklundDepartment of Oncology-Pathology, Cancer Center Karolinska CCK, Karolinska Institutet, Stockholm, Sweden.
Joseph CarlsonDepartment of Oncology-Pathology, Cancer Center Karolinska CCK, Karolinska Institutet, Stockholm, Sweden; Department of Pathology-Cytology, Radiumhemmet, Karolinska University Hospital, Stockholm, Sweden.
Maria ShoshanDepartment of Oncology-Pathology, Cancer Center Karolinska CCK, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial ovarian carcinoma (EOC), the major cause of gynaecological cancer death, is a heterogeneous disease classified into five subtypes. Each subtype has distinct clinical characteristics and is associated with different genetic risk factors and molecular events, but all are treated with surgery and platinum/taxane regimes. Tumour progression and chemoresistance is generally associated with major metabolic alterations, notably altered mitochondrial function(s). Here, we report for the first time that the expression of the mitochondrial regulators PGC1α and TFAM varies between EOC subtypes; furthermore, we have identified a profile in clear-cell carcinoma consisting of undetectability of PGC1α/TFAM, and low ERα/Ki-67. By contrast, high-grade serous carcinomas were characterised by a converse state of PGC1α/TFAM, ERα positivity and a high Ki-67 index. Interestingly, loss of PGC1α/TFAM and ERα was found also in a non-clear cell EOC cell line made highly resistant to platinum in vitro. Similar to clear-cell carcinomas, these resistant cells also showed accumulation of glycogen. Altogether, our data provide mechanistic insights into the chemoresistant nature of ovarian clear-cell carcinomas. Furthermore, these findings corroborate the need to take into account the diversity of EOC and to develop subtype specific treatment strategies.

Indexed as

Adenocarcinoma, Clear CellAdultAgedAged, 80 and overBiomarkers, TumorCell Line, TumorCystadenocarcinoma, SerousDisease ProgressionDNA-Binding ProteinsDrug Resistance, NeoplasmFemaleGlycogenHumansMiddle AgedMitochondrial ProteinsOvarian NeoplasmsBiomarkers, TumorDNA-Binding ProteinsGlycogenMitochondrial ProteinsPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPARGC1A protein, humanTFAM protein, humanTranscription Factors

Identifiers

PMID25243473
PMCPMC4170973
OpenAlexW2013935749

What OpenQuestion holds

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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.