Evidence map›Paper›PMID 36224382›Full record

ArticleMedical oncology (Northwood, London, England)2022

Identification and analysis of dysregulated fatty acid metabolism genes in breast cancer subtypes.

Umar Yousuf, Shazia Sofi, Aanisa Makhdoomi, Manzoor Ahmad Mir

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Genetic Associations ofAnimals : an open access journal from MDPI · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. CytochromeSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Introduction ofIranian journal of basic medical sciences · 2024
    Article
  20. 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.

Umar Yousuf *Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, J&K, 190006, India.
Shazia Sofi *Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, J&K, 190006, India.
Aanisa MakhdoomiDepartment of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, J&K, 190006, India.
Manzoor Ahmad MirDepartment of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, J&K, 190006, India. drmanzoor@kashmiruniversity.ac.in.ORCID http://orcid.org/0000-0003-3297-1402
University of Kashmir · IN

Funding

Jammu Kashmir Science Technology and Innovation Council Govt of J&K Grant NO. JKST&IC/SRE/885-87 Dated 27-10-2021
6 · The paper itself

Abstract

Breast cancer is one of the most aggressive and lethal types of transformation among women. An anomaly of normal fatty acid metabolism is acknowledged as a critical trigger for malignant transformations including breast cancer, but the prospect of targeting fatty acid metabolism for the treatment of malignancy has remained unrecognized so far. It has been observed that specific fatty acid metabolism genes are involved in the commencement and development of breast cancer. These specific genes have also been observed to be related to different isotypes/molecular subtypes of breast cancer. The main purpose of this study was to scrutinize the prognostic significance, functional role, and expression pattern of fatty acid metabolism genes. In-Silico tools like TCGA BrCA, Gepia2, Ualcan Analysis, UCSC Xena, Kaplan-Meier plotter, Bc-gene EXminer, String, gene ontology, and KEGG databases, were used to assess the expression pattern of the fatty acid metabolism genes in breast cancer patients and also among the different molecular sub-types of breast cancer. Differential gene expression analysis revealed dysregulation of FABP4, FABP5, PLIN1, PLIN2, PLIN4, PLIN5, LPIN1, MGLL, PNPLA2, PNPLA7, ACSL1, and ACOX2 showing a fold change >  ± 1.5. Also, most of these genes show downregulation in Ualcan analysis of different isotypes/molecular subtypes of breast cancer. The study reveals that the screened genes i.e., FABP4, FABP5, PLIN1, PLIN2, PLIN4, PLIN5, LPIN1, MGLL, PNPLA2, PNPLA7, ACSL1, and ACOX2 can be used as biomarkers that reveal poor prognosis and may serve as therapeutic targets for the treatment of breast cancer.

Indexed as

Breast NeoplasmsBiomarkers, TumorFatty Acid-Binding ProteinsFatty AcidsFemaleGene Expression Regulation, NeoplasticGene OntologyHumansPhosphatidate PhosphatasePrognosisBiomarkers, TumorFABP5 protein, humanFatty Acid-Binding ProteinsFatty AcidsLPIN1 protein, humanPhosphatidate PhosphataseBioinformaticsBreast cancerDysregulated genesExpression patternFatty acid metabolismGene ontologyPrognosisSurvival probability

Identifiers

PMID36224382
OpenAlexW4304734167

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.