Evidence map›Paper›PMID 29024936›Full record

ArticleBritish journal of cancer2017

Glucose insult elicits hyperactivation of cancer stem cells through miR-424-cdc42-prdm14 signalling axis.

Sushmita Bose Nandy, Alexis Orozco, Rebecca Lopez-Valdez, Rene Roberts, Ramadevi Subramani, Arunkumar Arumugam, Alok Kumar Dwivedi, Viktoria Stewart, Gautham Prabhakar, Stephanie Jones and 1 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  6. MicroRNAs: A Link between Mammary Gland Development and Breast Cancer.International journal of molecular sciences · 2022
    Review
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  8. Review
  9. Therapeutic siRNA targeting the cancer cell stemness regulator PRDI-BF1 and RIZ domain zinc finger protein 14.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2022
    Article
  10. Article
  11. Review
  12. PRDM14 promotes malignant phenotype and correlates with poor prognosis in colorectal cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Article
  13. Multifaceted Role of PRDM Proteins in Human Cancer.International journal of molecular sciences · 2020
    Review
  14. Role of miRNA-424 in Cancers.OncoTargets and therapy · 2020
    Review
  15. Review
  16. Article
  17. Article
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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 3 institutions in 1 country.

Sushmita Bose NandyDepartment of Biomedical Sciences, Center of Emphasis in Cancer Research, Texas Tech University Health Sciences Center El Paso, El Paso, TX 79905, USA.
Alexis OrozcoGraduate School of Biomedical Sciences, Texas Tech University Health Sciences Center El Paso, El Paso, TX 79905, USA.
Rebecca Lopez-ValdezDepartment of Biomedical Sciences, Center of Emphasis in Cancer Research, Texas Tech University Health Sciences Center El Paso, El Paso, TX 79905, USA.
Rene RobertsDepartment of Biomedical Sciences, Paul L Foster School of Medicine, Texas Tech University Health Sciences Center, Center of Excellence in Cancer Research, El Paso, TX 79905, USA.
Ramadevi SubramaniDepartment of Biomedical Sciences, Center of Emphasis in Cancer Research, Texas Tech University Health Sciences Center El Paso, El Paso, TX 79905, USA.
Arunkumar ArumugamDepartment of Biomedical Sciences, Center of Emphasis in Cancer Research, Texas Tech University Health Sciences Center El Paso, El Paso, TX 79905, USA.
Alok Kumar DwivediBiostatistics and Epidemiology Consulting Laboratory, Texas Tech University Health Sciences Center El Paso, El Paso, TX 79905, USA.
Viktoria StewartDepartment of Biomedical Sciences, Paul L Foster School of Medicine, Texas Tech University Health Sciences Center, Center of Excellence in Cancer Research, El Paso, TX 79905, USA.
Gautham PrabhakarDepartment of Biomedical Sciences, Paul L Foster School of Medicine, Texas Tech University Health Sciences Center, Center of Excellence in Cancer Research, El Paso, TX 79905, USA.
Stephanie JonesDepartment for Biological Science, University of Texas El Paso, El Paso, TX 79902, USA.
Rajkumar LakshmanaswamyDepartment of Biomedical Sciences, Center of Emphasis in Cancer Research, Texas Tech University Health Sciences Center El Paso, El Paso, TX 79905, USA.
Texas Tech University Health Sciences Center · USTexas Tech University · USThe University of Texas at El Paso · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMeta-analysis shows that women with diabetes have a 20% increased risk of breast cancer and also an increased risk for distant metastasis and mortality. The molecular mechanisms for distant metastasis and mortality in breast cancer patients with diabetes are not very well understood.

methodsWe compared the effect of physiological (5 mM) and diabetic (10 mM) levels of glucose on malignant breast epithelial cell invasion and stemness capabilities. We performed microRNA array to determine the dysregulated microRNAs in hyperglycaemic conditions and performed functional and molecular analysis of the gene targets.

resultsHyperglycaemia leads to hyperactivation of cancer stem cell pool and enhances invasive ability of breast cancer cells. MiR-424 seems to be a key regulator of cancer cell stemness and invasion. Knockdown of miR-424 in cancer cells under euglycaemic conditions leads to enhanced invasion and stem cell activity, whereas ectopic expression of miR-424 in cancer cells under hyperglycaemic conditions results in suppressed invasion and stem cell activity. Cdc42, a target of miR-424, influences cancer stem cell activity by positively regulating prdm14 through activation of pak1 (p-21-activated kinase 1) and stat5.

conclusionsOur findings establish miR-424→︀cdc42→︀prdm14 axis as a key molecular signalling cascade that might influence breast cancer progression in diabetic patients through hyperactivation of cancer stem cells.

Indexed as

AnimalsBreast Neoplasmscdc42 GTP-Binding ProteinCell Line, TumorDNA-Binding ProteinsFemaleGlucoseHumansHyperglycemiaMiceMicroRNAsNeoplasm InvasivenessNeoplastic Stem CellsRepressor ProteinsRNA-Binding ProteinsSignal Transductioncdc42 GTP-Binding ProteinDNA-Binding ProteinsGlucoseMicroRNAsMIRN424 microrna, humanPRDM14 protein, humanRepressor ProteinsRNA-Binding ProteinsTranscription Factors

Identifiers

PMID29024936
PMCPMC5729435
OpenAlexW2762548324

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.