Evidence map›Paper›PMID 28092823›Full record

ArticleNeoplasia (New York, N.Y.)2017

pH, Lactate, and Hypoxia: Reciprocity in Regulating High-Affinity Monocarboxylate Transporter Expression in Glioblastoma.

James P Caruso, Brandon J Koch, Philip D Benson, Elsa Varughese, Michael D Monterey, Amy E Lee, Ajal M Dave, Sam Kiousis, Andrew E Sloan, Saroj P Mathupala

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Metabolic Rewiring in Glioblastoma Cancer:Frontiers in oncology · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Cell communication and signaling : CCS · 2019
    Article
  15. Article
  16. 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

10 authors at 3 institutions in 1 country.

James P CarusoDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI 48201; Program in Biophysics, University of Michigan, Ann Arbor, MI 48109.
Brandon J KochDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI 48201; Department of Biochemistry and Molecular Biology, Rollins College, Winter Park, FL 32789.
Philip D BensonDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI 48201.
Elsa VarugheseDepartment of Physics & Astronomy, Wayne State University College of Liberal Arts & Sciences, Detroit, MI, 48201.
Michael D MontereyDepartment of Neurosurgery & Basic Medical Sciences Program, Wayne State University School of Medicine, Detroit, MI 48201.
Amy E LeeDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI 48201.
Ajal M DaveDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI 48201.
Sam KiousisDepartment of Neurosurgery, Wayne State University School of Medicine, Detroit, MI 48201.
Andrew E SloanDepartment of Neurological Surgery, University Hospitals-Case Medical Center & Case Comprehensive Cancer Center, Cleveland, OH 44106.
Saroj P MathupalaDepartment of Neurosurgery and Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI 48201. Electronic address: ah1244@wayne.edu.
Wayne State University · USThe Barbara Ann Karmanos Cancer Institute · USUniversity Hospitals Case Medical Center · US

Funding

Lactate Transport as a Therapeutic Target in GliomaR01CA116257 · NCI · WAYNE STATE UNIVERSITY · PI MATHUPALA, SAROJ PRIYANTHA · 2006 to 2010
$1.2M
NCI NIH HHS R01 CA116257
6 · The paper itself

Abstract

Highly malignant brain tumors harbor the aberrant propensity for aerobic glycolysis, the excessive conversion of glucose to lactic acid even in the presence of ample tissue oxygen. Lactic acid is rapidly effluxed to the tumor microenvironment via a group of plasma-membrane transporters denoted monocarboxylate transporters (MCTs) to prevent "self-poisoning." One isoform, MCT2, has the highest affinity for lactate and thus should have the ability to respond to microenvironment conditions such as hypoxia, lactate, and pH to help maintain high glycolytic flux in the tumor. Yet, MCT2 is considered to not respond to hypoxia, which is counterintuitive. Its response to tumor lactate has not been reported. In this report, we experimentally identify the transcription initiation site/s for MCT2 in astrocytes (normal) and glioma (tumor). We then use a BACmid library to isolate a 4.2-kbp MCT2 promoter-exon I region and examine promoter response to glycolysis-mediated stimuli in glioma cells. Reporter analysis of nested-promoter constructs indicated response of MCT2 to hypoxia, pH, lactate, and glucose, the major physiological "players" that facilitate a tumor's growth and proliferation. Immunoblot analysis of native MCT2 expression under altered pH and hypoxia reflected the reporter data. The pH-mediated gene-regulation studies we describe are the first to record H

Indexed as

Hydrogen-Ion ConcentrationAstrocytesCell HypoxiaCell Line, TumorCells, CulturedGene ExpressionGene Expression Regulation, NeoplasticGenes, ReporterGlioblastomaGliomaHumansHypoxiaLactic AcidMonocarboxylic Acid TransportersMutationPromoter Regions, GeneticLactic AcidMonocarboxylic Acid TransportersSLC16A7 protein, human

Identifiers

PMID28092823
PMCPMC5238458
OpenAlexW2573577038

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.