Evidence map›Paper›PMID 23918800›Full record

ArticleMolecular and cellular biology2013

Molecular mechanism of SLC5A8 inactivation in breast cancer.

Selvakumar Elangovan, Rajneesh Pathania, Sabarish Ramachandran, Sudha Ananth, Ravi N Padia, Sonne R Srinivas, Ellappan Babu, Lesleyann Hawthorn, Patricia V Schoenlein, Thomas Boettger and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2013. 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
1.5field-weighted citation impact, top 18% 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, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. MicroRNAs and Their Inhibition in ModulatingInternational journal of molecular sciences · 2025
    Article
  4. Article
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  6. Prognostic value ofFrontiers in oncology · 2023
    Article
  7. Article
  8. Review
  9. Cancer research · 2020
    Article
  10. Frontiers in oncology · 2020
    Article
  11. Article
  12. Article
  13. Deficiency of Dietary Fiber inCanadian journal of gastroenterology & hepatology · 2019
    Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Frontiers in cellular and infection microbiology · 2016
    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

14 authors at 4 institutions in 3 countries.

Selvakumar ElangovanDepartments of Biochemistry and Molecular Biology.
Rajneesh Pathania
Sabarish Ramachandran
Sudha Ananth
Ravi N Padia
Sonne R Srinivas
Ellappan Babu
Lesleyann Hawthorn
Patricia V Schoenlein
Thomas Boettger
Sylvia B Smith
Puttur D Prasad
Vadivel Ganapathy
Muthusamy Thangaraju
University of Georgia · USAugusta University · USAugusta University Health · USMax Planck Society · DE

Funding

Tumor-Suppressive Function of SLC5A8 in Mammary Gland and its Relevance to BreastR01CA131402 · NCI · AUGUSTA UNIVERSITY · PI THANGARAJU, MUTHUSAMY · 2008 to 2012
$1.3M
NCI NIH HHS BC074289NCI NIH HHS R01 CA131402
6 · The paper itself

Abstract

SLC5A8 is a putative tumor suppressor that is inactivated in more than 10 different types of cancer, but neither the oncogenic signaling responsible for SLC5A8 inactivation nor the functional relevance of SLC5A8 loss to tumor growth has been elucidated. Here, we identify oncogenic HRAS (HRAS(G12V)) as a potent mediator of SLC5A8 silencing in human nontransformed normal mammary epithelial cell lines and in mouse mammary tumors through DNMT1. Further, we demonstrate that loss of Slc5a8 increases cancer-initiating stem cell formation and promotes mammary tumorigenesis and lung metastasis in an HRAS-driven murine model of mammary tumors. Mammary-gland-specific overexpression of Slc5a8 (mouse mammary tumor virus-Slc5a8 transgenic mice), as well as induction of endogenous Slc5a8 in mice with inhibitors of DNA methylation, protects against HRAS-driven mammary tumors. Collectively, our results provide the tumor-suppressive role of SLC5A8 and identify the oncogenic HRAS as a mediator of tumor-associated silencing of this tumor suppressor in mammary glands. These findings suggest that pharmacological approaches to reactivate SLC5A8 expression in tumor cells have potential as a novel therapeutic strategy for breast cancer treatment.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBreast NeoplasmsCarcinogenesisCation Transport ProteinsCell LineCell Line, TumorDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesFemaleHCT116 CellsHumansImmunoblottingMaleMCF-7 CellsMiceCation Transport ProteinsDNA (Cytosine-5-)-Methyltransferase 1DNA (Cytosine-5-)-MethyltransferasesDNMT1 protein, humanDnmt1 protein, mouseHRAS protein, humanMonocarboxylic Acid TransportersProto-Oncogene Proteins p21(ras)SLC5A8 protein, human

Identifiers

PMID23918800
PMCPMC3811868
OpenAlexW2123312374

What OpenQuestion holds

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Registered trials

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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.