Evidence map›Paper›PMID 39538154›Full record

ArticleBMC cancer2024

Prognostic role of Androgen Receptor splice variant 7 (AR-V7) in the pathogenesis of breast cancer.

Tryambak Pratap Srivastava, Swati Ajmeriya, Isha Goel, Joyeeta Talukdar, Anurag Srivastava, Rajinder Parshad, S V S Deo, Sandeep R Mathur, Ajay Gogia, Avdhesh Rai and 2 more

Abstract read
In one paragraph

Article in BMC cancer, 2024. 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
–field-weighted citation impact
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.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  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

12 authors.

Tryambak Pratap Srivastava *Department of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.
Swati AjmeriyaDepartment of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.
Isha GoelDepartment of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.
Joyeeta TalukdarDepartment of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.
Anurag SrivastavaDepartment of Surgical Disciplines, All India Institute of Medical Sciences, New Delhi, India.
Rajinder ParshadDepartment of Surgical Disciplines, All India Institute of Medical Sciences, New Delhi, India.
S V S DeoDepartment of Surgical Oncology, All India Institute of Medical Sciences, New Delhi, India.
Sandeep R MathurDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, India.
Ajay GogiaDepartment of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India.
Avdhesh RaiDBT Centre For Molecular Biology and Cancer Research, Dr. Bhubaneswar Borooah Cancer Institute, Guwahati, India.
Ruby DharDepartment of Biochemistry, All India Institute of Medical Sciences, New Delhi, India. rubydhar@gmail.com.
Subhradip KarmakarDepartment of Biochemistry, All India Institute of Medical Sciences, New Delhi, India. subhradip.k@aiims.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Androgen Receptor (AR) has emerged as an endocrine therapy target in Breast Cancer, exhibiting up to 80% expression in clinical cases. AR-V7, a constitutively activated splice variant of AR with a truncated ligand-binding domain (LBD), demonstrates ligand-independent transcriptional activity and resistance to nonsteroidal antiandrogens like Bicalutamide or Enzalutamide, targeting the LBD. In metastatic prostate cancer, elevated AR-V7 levels lead to therapeutic resistance and increased metastasis.

methodsIn this study, we evaluated the expression of AR and AR-V7 in cell lines and a cohort of 89 patients undergoing surgical intervention for treatment-naïve breast cancer. Further clinicopathological correlations and survival analysis were performed to evaluate the relationship between the AR and AR-V7 expression and clinical outcomes.

resultsAR-V7/AR-FL ratio was elevated in the TNBC cell line and downregulation of AR-FL upon AR antagonists' treatment led to a compensatory increase in AR-V7. Clinical samples showed significantly elevated expression of AR and AR-V7 in tumors compared to control cases. Further clinicopathological correlation revealed aggressive clinical traits, higher pathological grades, and poor survival with AR-V7 expression.

conclusionsOur study unravels AR-V7 as a marker for poor clinical outcomes, predicting breast cancer aggressiveness, and encourages consideration of AR-V7 as a probable target for therapeutic intervention.

Indexed as

Breast NeoplasmsReceptors, AndrogenAdultAgedAlternative SplicingBiomarkers, TumorCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedNitrilesPhenylthiohydantoinPrognosisProtein IsoformsTriple Negative Breast NeoplasmsAR protein, humanBiomarkers, TumorNitrilesPhenylthiohydantoinProtein IsoformsReceptors, AndrogenAndrogen receptorAR-V7BiomarkerBreast cancerSplice variant

Identifiers

PMID39538154
PMCPMC11562864

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.