Evidence map›Paper›PMID 35411033›Full record

ArticleOncogene2022

Fatty acid oxidation enzyme Δ3, Δ2-enoyl-CoA isomerase 1 (ECI1) drives aggressive tumor phenotype and predicts poor clinical outcome in prostate cancer patients.

Yogesh M Bramhecha, Karl-Philippe Guérard, Étienne Audet-Walsh, Shaghayegh Rouzbeh, Ola Kassem, Erwan Pernet, Eleonora Scarlata, Lucie Hamel, Fadi Brimo, Maziar Divangahi and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Membrane Stress and Ferroptosis: Lipid Dynamics in Cancer.International journal of molecular sciences · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Emerging Hallmarks of Metabolic Reprogramming in Prostate Cancer.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Review
  13. Article
  14. 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

14 authors at 1 institution in 1 country.

Yogesh M BramhechaDepartment of Surgery, Division of Urology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Karl-Philippe GuérardDepartment of Surgery, Division of Urology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Étienne Audet-WalshGoodman Cancer Research Centre, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.ORCID http://orcid.org/0000-0002-7710-8365
Shaghayegh RouzbehDepartment of Surgery, Division of Urology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Ola KassemDepartment of Surgery, Division of Urology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Erwan PernetMeakins-Christie Laboratories, Department of Medicine, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Eleonora ScarlataDepartment of Surgery, Division of Urology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Lucie HamelDepartment of Surgery, Division of Urology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Fadi BrimoDepartment of Pathology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Maziar DivangahiMeakins-Christie Laboratories, Department of Medicine, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Armen G AprikianDepartment of Surgery, Division of Urology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Simone ChevalierDepartment of Surgery, Division of Urology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Vincent GiguèreGoodman Cancer Research Centre, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada.ORCID http://orcid.org/0000-0001-9567-3694
Jacques LapointeDepartment of Surgery, Division of Urology, McGill University and the Research Institute of the McGill University Health Centre, Montreal, QC, Canada. Jacques.lapointe@mcgill.ca.ORCID http://orcid.org/0000-0002-4586-8052
McGill University Health Centre · CA

Funding

CIHR
6 · The paper itself

Abstract

Prostate cancer (PCa) metastases are highly enriched with genomic alterations including a gain at the 16p13.3 locus, recently shown to be associated with disease progression and poor clinical outcome. ECI1, residing at the 16p13.3 gain region, encodes Δ3, Δ2-Enoyl-CoA Delta Isomerase 1 (ECI1), a key mitochondrial fatty acid β-oxidation enzyme. Although deregulated mitochondrial fatty acid β-oxidation is known to drive PCa pathogenesis, the role of ECI1 in PCa is still unknown. We investigated the impacts of ECI1 on PCa phenotype in vitro and in vivo by modulating its expression in cell lines and assessed the clinical implications of its expression in human prostate tissue samples. In vitro, ECI1 overexpression increased PCa cell growth while ECI1 deficiency reduced its growth. ECI1 also enhanced colony formation, cell motility, and maximal mitochondrial respiratory capacity. In vivo, PCa cells stably overexpressing ECI1 injected orthotopically in nude mice formed larger prostate tumors with higher number of metastases. Immunohistochemistry analysis of the human tissue microarray representing 332 radical prostatectomy cases revealed a stronger ECI1 staining in prostate tumors compared to corresponding benign tissues. ECI1 expression varied amongst tumors and was higher in cases with 16p13.3 gain, high Gleason grade, and advanced tumor stage. ECI1 overexpression was a strong independent predictor of biochemical recurrence after adjusting for known clinicopathologic parameters (hazard ratio: 3.65, P < 0.001) or the established CAPRA-S score (hazard ratio: 3.95, P < 0.001). ECI1 overexpression was also associated with significant increased risk of distant metastasis and reduced overall survival. Overall, this study demonstrates the functional capacity of ECI1 in PCa progression and highlights the clinical implication of ECI1 as a potential target for the management of PCa.

Indexed as

Dodecenoyl-CoA IsomeraseProstatic NeoplasmsAnimalsFatty AcidsHumansMaleMiceMice, NudePhenotypeDodecenoyl-CoA IsomeraseECI1 protein, humanFatty Acids

Identifiers

PMID35411033
OpenAlexW4223509603

What OpenQuestion holds

Textmetadata
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.