Evidence map›Paper›PMID 35399074›Full record

ArticleBMC cancer2022

Assessment of the diagnostic and prognostic relevance of ACAT1 and CE levels in plasma, peritoneal fluid and tumor tissue of epithelial ovarian cancer patients - a pilot study.

Vijayalakshmi Ayyagari, Maio Li, Zvi Pasman, Xinjia Wang, Somaja Louis, Paula Diaz-Sylvester, Kathleen Groesch, Teresa Wilson, Laurent Brard

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The emerging role of cholesterol metabolism in gynecologic cancer development and therapy.Apoptosis : an international journal on programmed cell death · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Dysregulation of Cholesterol Homeostasis in Ovarian Cancer.Current oncology (Toronto, Ont.) · 2023
    Review
  9. 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

9 authors at 2 institutions in 1 country.

Vijayalakshmi AyyagariDepartment of Obstetrics and Gynecology, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Maio LiDepartment of Obstetrics and Gynecology, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Zvi PasmanDepartment of Obstetrics and Gynecology, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Xinjia WangDepartment of Obstetrics and Gynecology, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Somaja LouisDepartment of Obstetrics and Gynecology, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Paula Diaz-SylvesterDepartment of Obstetrics and Gynecology, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Kathleen GroeschDepartment of Obstetrics and Gynecology, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Teresa WilsonDepartment of Obstetrics and Gynecology, Southern Illinois University School of Medicine, Springfield, Illinois, USA.
Laurent BrardDepartment of Obstetrics and Gynecology, Southern Illinois University School of Medicine, Springfield, Illinois, USA. lbrard@siumed.edu.
Southern Illinois University School of Medicine · USIllinois College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAbnormal accumulation of acyl-CoA cholesterol acyltransferase-1 (ACAT1) and ACAT1-mediated cholesterol esterified with fatty acids (CE) contribute to cancer progression in various cancers. Our findings of increased CE and ACAT1 levels in epithelial ovarian cancer (EOC) cell lines prompted us to investigate whether such an increase occurs in primary clinical samples obtained from human subjects diagnosed with EOC. We evaluated the diagnostic/prognostic potential of ACAT1 and CE in EOC by: 1) assessing ACAT1 and CE levels in plasma, peritoneal fluid, and ovarian/tumor tissues; 2) assessing diagnostic performance by Receiver Operating Characteristic (ROC) analysis; and 3) comparing expression of ACAT1 and CE with that of tumor proliferation marker, Ki67.

methodsACAT1 protein levels in plasma, peritoneal fluid and tissue were measured via enzyme-linked immunosorbent assay. Tissue expression of ACAT1 and Ki67 proteins were confirmed by immunohistochemistry and mRNA transcript levels were evaluated using quantitative real-time polymerase chain reaction (qRT-PCR). CE levels were assessed in plasma, peritoneal fluid (colorimetric assay) and in tissue (thin layer chromatography).

resultsPreoperative levels of ACAT1 and CE on the day of surgery were significantly higher in tissue and peritoneal fluid from EOC patients vs. the non-malignant group, which included subjects with benign tumors and normal ovaries; however, no significant differences were observed in plasma. In tissue and peritoneal fluid, positive correlations were observed between CE and ACAT1 levels, as well as between ACAT1/CE and Ki67.

conclusionsACAT1 and CE accumulation may be linked to the aggressive potential of EOC; therefore, these mediators may be useful biomarkers for EOC prognosis and target-specific treatments.

Indexed as

Acetyl-CoA C-AcetyltransferaseCarcinoma, Ovarian EpithelialOvarian NeoplasmsAcyltransferasesAscitic FluidBiomarkers, TumorCholesterolFatty AcidsFemaleHumansKi-67 AntigenPilot ProjectsPrognosisACAT1 protein, humanAcetyl-CoA C-AcetyltransferaseAcyltransferasesBiomarkers, TumorCholesterolFatty AcidsKi-67 AntigenACAT1CEEpithelial ovarian cancerKi67

Identifiers

PMID35399074
PMCPMC8994887
OpenAlexW4223470676

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.