Evidence map›Paper›PMID 31694904›Full record

ArticleCancer research2020

A Novel Bioengineered miR-127 Prodrug Suppresses the Growth and Metastatic Potential of Triple-Negative Breast Cancer Cells.

Maxine Umeh-Garcia, Catalina Simion, Pui-Yan Ho, Neelu Batra, Anastasia L Berg, Kermit L Carraway, Aiming Yu, Colleen Sweeney

Abstract read
In one paragraph

Article in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–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

35 citing papers in PubMed.

  1. Review
  2. Article
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  9. Article
  10. Review
  11. Article
  12. Review
  13. RNAi-Based Therapeutics and Novel RNA Bioengineering Technologies.The Journal of pharmacology and experimental therapeutics · 2023
    Review
  14. Review
  15. Article
  16. Emerging Roles of NANOS RNA-Binding Proteins in Cancer.International journal of molecular sciences · 2022
    Article
  17. Article
  18. Correlation of serum miR-127 level with severity and prognosis of sepsis.American journal of translational research · 2022
    Article
  19. Article
  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

8 authors.

Maxine Umeh-GarciaDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Sacramento, California.
Catalina SimionDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Sacramento, California.
Pui-Yan HoDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Sacramento, California.
Neelu BatraDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Sacramento, California.
Anastasia L BergDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Sacramento, California.ORCID 0000-0002-1021-4278
Kermit L CarrawayDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Sacramento, California.
Aiming YuDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Sacramento, California.
Colleen SweeneyDepartment of Biochemistry and Molecular Medicine, University of California, Davis, Sacramento, California. casweeney@ucdavis.edu.

Funding

Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura Marcu · 2002 to 2026
$84.9M
UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
Novel bioengineered microRNA therapeutics for lung cancerR01CA225958 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Aiming Yu · 2019 to 2026
$3.7M
Predoctoral Training in Pharmacological SciencesT32GM099608 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2012 to 2021
$2.2M
Recombinant microRNAs in xenobiotic dispositionR01GM113888 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI YU, AIMING · 2016 to 2019
$1.3M
NCI NIH HHS P30 CA093373NCI NIH HHS R01 CA225958NIGMS NIH HHS R01 GM113888NIGMS NIH HHS T32 GM007377NIGMS NIH HHS T32 GM099608
6 · The paper itself

Abstract

miR-127 is downregulated in breast cancer, where it has been shown to suppress the proliferation, migration, and invasion of breast cancer cells. In triple-negative breast cancer (TNBC), miR-127 downregulation correlates with decreased disease-free and overall patient survival. Tumor suppressor miRNAs may hold therapeutic promise but progress has been limited by several factors, including the lability and high cost of miRNA mimics. Here, we take a novel approach to produce a miR-127 prodrug (miR-127

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntineoplastic AgentsApoptosisBiomarkers, TumorCell ProliferationFemaleHumansLung NeoplasmsLymphatic MetastasisMiceMice, Inbred NODMice, SCIDMicroRNAsProdrugsPrognosisAntineoplastic AgentsBiomarkers, TumorMicroRNAsMIRN127 microRNA, humanProdrugsSOXC Transcription Factors

Identifiers

PMID31694904
PMCPMC7002233

What OpenQuestion holds

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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.