Evidence map›Paper›PMID 31006104›Full record

ArticleBreast cancer research and treatment2019

A novel RNA aptamer identifies plasma membrane ATP synthase beta subunit as an early marker and therapeutic target in aggressive cancer.

S Speransky, P Serafini, J Caroli, S Bicciato, M E Lippman, N H Bishopric

Open access · hybridAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

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  6. Proteomics Investigation of the Impact of theInternational journal of molecular sciences · 2023
    Article
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  12. Aptamer-Based Tumor-Targeted Diagnosis and Drug Delivery.Advances in experimental medicine and biology · 2023
    Review
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  14. Article
  15. Review
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  17. Article
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  19. Natural products and other inhibitors of FEuropean journal of medicinal chemistry · 2020
    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

6 authors at 3 institutions in 2 countries.

S SperanskyDepartment of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, USA.
P SerafiniDepartment of Microbiology & Immunology, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, USA.
J CaroliCenter for Genome Research, Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
S BicciatoCenter for Genome Research, Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
M E LippmanDepartment of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, USA.
N H BishopricDepartment of Medicine, Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, USA. nhb20@georgetown.edu.
Sylvester Comprehensive Cancer Center · USUniversity of Modena and Reggio Emilia · ITGeorgetown University · US

Funding

Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI George S. Grills · 2019 to 2026
$24.1M
AIRC Special Program Molecular Clinical Oncology 10016NCI NIH HHS P30 CA240139U.S. Department of Defense W81XWH1210034
6 · The paper itself

Abstract

purposePrimary breast and prostate cancers can be cured, but metastatic disease cannot. Identifying cell factors that predict metastatic potential could guide both prognosis and treatment.

methodsWe used Cell-SELEX to screen an RNA aptamer library for differential binding to prostate cancer cell lines with high vs. low metastatic potential. Mass spectroscopy, immunoblot, and immunohistochemistry were used to identify and validate aptamer targets. Aptamer properties were tested in vitro, in xenograft models, and in clinical biopsies. Gene expression datasets were queried for target associations in cancer.

resultsWe identified a novel aptamer (Apt63) that binds to the beta subunit of F

conclusionEcto-ATP5B binding by Apt63 may disrupt an essential survival mechanism in a subset of tumors with high metastatic potential, and defines a novel category of cancers with potential vulnerability to ATP5B-targeted therapy. Apt63 is a unique tool for elucidating the function of surface ATP synthase, and potentially for predicting and treating metastatic breast and prostate cancer.

Indexed as

Administration, IntravenousAnimalsAptamers, NucleotideBiomarkers, TumorBreast NeoplasmsCell Line, TumorCell MembraneCell ProliferationCell SurvivalEarly Detection of CancerFemaleGene Expression Regulation, NeoplasticHumansMaleMCF-7 CellsMiceAptamers, NucleotideATP5F1B protein, humanBiomarkers, TumorMitochondrial Proton-Translocating ATPasesAptamerBreast cancerCell-SELEXEcto-ATP synthaseMetastasisProstate cancer

Identifiers

PMID31006104
PMCPMC6555781
OpenAlexW2938581263

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.