Evidence map›Paper›PMID 33031638›Full record

ArticleMolecular oncology2020

The FABP12/PPARγ pathway promotes metastatic transformation by inducing epithelial-to-mesenchymal transition and lipid-derived energy production in prostate cancer cells.

Rong-Zong Liu, Won-Shik Choi, Saket Jain, Deepak Dinakaran, Xia Xu, Woo Hyun Han, Xiao-Hong Yang, Darryl D Glubrecht, Ronald B Moore, Hélène Lemieux and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Dual function of activated PPARγ by ligands on tumor growth and immunotherapy.Medical oncology (Northwood, London, England) · 2024
    Review
  8. Article
  9. Article
  10. Metabolic heterogeneity in cancer.Nature metabolism · 2024
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Emerging Hallmarks of Metabolic Reprogramming in Prostate Cancer.International journal of molecular sciences · 2023
    Review
  19. Review
  20. 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

11 authors at 1 institution in 1 country.

Rong-Zong LiuDepartment of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada.ORCID 0000-0001-8625-3188
Won-Shik ChoiDepartment of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada.
Saket JainDepartment of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada.
Deepak DinakaranDepartment of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada.
Xia XuDepartment of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada.
Woo Hyun HanFaculty Saint-Jean, University of Alberta, Edmonton, AB, Canada.
Xiao-Hong YangDepartment of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada.
Darryl D GlubrechtDepartment of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada.
Ronald B MooreDepartment of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada.
Hélène LemieuxFaculty Saint-Jean, University of Alberta, Edmonton, AB, Canada.
Roseline GodboutDepartment of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB, Canada.ORCID 0000-0002-4779-9265
University of Alberta · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early stage localized prostate cancer (PCa) has an excellent prognosis; however, patient survival drops dramatically when PCa metastasizes. The molecular mechanisms underlying PCa metastasis are complex and remain unclear. Here, we examine the role of a new member of the fatty acid-binding protein (FABP) family, FABP12, in PCa progression. FABP12 is preferentially amplified and/or overexpressed in metastatic compared to primary tumors from both PCa patients and xenograft animal models. We show that FABP12 concurrently triggers metastatic phenotypes (induced epithelial-to-mesenchymal transition (EMT) leading to increased cell motility and invasion) and lipid bioenergetics (increased fatty acid uptake and accumulation, increased ATP production from fatty acid β-oxidation) in PCa cells, supporting increased reliance on fatty acids for energy production. Mechanistically, we show that FABP12 is a driver of PPARγ activation which, in turn, regulates FABP12's role in lipid metabolism and PCa progression. Our results point to a novel role for a FABP-PPAR pathway in promoting PCa metastasis through induction of EMT and lipid bioenergetics.

Indexed as

Energy MetabolismEpithelial-Mesenchymal TransitionCell Line, TumorCell MovementCell Transformation, NeoplasticDisease ProgressionFatty Acid-Binding ProteinsGene DosageHumansLipidsMaleNeoplasm InvasivenessNeoplasm MetastasisPPAR gammaProstatic NeoplasmsSignal TransductionFABP12 protein, humanFatty Acid-Binding ProteinsLipidsPPAR gammabioenergeticsepithelial-mesenchymal transitionfatty acid-binding proteinsmetastasisperoxisome proliferator-activated receptor gammaprostate cancer

Identifiers

PMID33031638
PMCPMC7718947
OpenAlexW3091801559

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.