Evidence map›Paper›PMID 27127175›Full record

ArticleOncotarget2016

Monocarboxylate transporter 1 contributes to growth factor-induced tumor cell migration independent of transporter activity.

Alana L Gray, David T Coleman, Runhua Shi, James A Cardelli

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Histone lactylation: from tumor lactate metabolism to epigenetic regulation.International journal of biological sciences · 2024
    Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Heteromeric Solute Carriers: Function, Structure, Pathology and Pharmacology.Advances in experimental medicine and biology · 2021
    Review
  8. Article
  9. The Crosstalk between Microbiome and Immune Response in Gastric Cancer.International journal of molecular sciences · 2020
    Review
  10. Article
  11. Monocarboxylate transporters in cancer.Molecular metabolism · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

4 authors at 1 institution in 1 country.

Alana L GrayLouisiana State University Health Sciences Center-Shreveport, Shreveport, LA, USA.
David T ColemanLouisiana State University Health Sciences Center-Shreveport, Shreveport, LA, USA.
Runhua ShiLouisiana State University Health Sciences Center-Shreveport, Shreveport, LA, USA.
James A CardelliLouisiana State University Health Sciences Center-Shreveport, Shreveport, LA, USA.
Louisiana State University Health Sciences Center Shreveport · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor progression to metastatic disease contributes to the vast majority of incurable cancer. Understanding the processes leading to advanced stage cancer is important for the development of future therapeutic strategies. Here, we establish a connection between tumor cell migration, a prerequisite to metastasis, and monocarboxylate transporter 1 (MCT1). MCT1 transporter activity is known to regulate aspects of tumor progression and, as such, is a clinically relevant target for treating cancer. Knockdown of MCT1 expression caused decreased hepatocyte growth factor (HGF)-induced as well as epidermal growth factor (EGF)-induced tumor cell scattering and wound healing. Western blot analysis suggested that MCT1 knockdown (KD) hinders signaling through the HGF receptor (c-Met) but not the EGF receptor. Exogenous, membrane-permeable MCT1 substrates were not able to rescue motility in MCT1 KD cells, nor was pharmacologic inhibition of MCT1 able to recapitulate decreased cell motility as seen with MCT1 KD cells, indicating transporter activity of MCT1 was dispensable for EGF- and HGF-induced motility. These results indicate MCT1 expression, independent of transporter activity, is required for growth factor-induced tumor cell motility. The findings presented herein suggest a novel function for MCT1 in tumor progression independent of its role as a monocarboxylate transporter.

Indexed as

Cell Line, TumorCell MovementEpidermal Growth FactorGene Expression Regulation, NeoplasticHepatocyte Growth FactorHumansLactic AcidMonocarboxylate Transport Protein 1Monocarboxylic Acid TransportersMuscle ProteinsNeoplasm InvasivenessPhosphorylationProto-Oncogene Proteins c-metRNA InterferenceSignal TransductionSymportersEpidermal Growth FactorHepatocyte Growth FactorLactic AcidMET protein, humanMonocarboxylate Transport Protein 1Monocarboxylic Acid TransportersMuscle ProteinsProto-Oncogene Proteins c-metSLC16A4 protein, humanSymporterscancerEGFHGFMCT1motility

Identifiers

PMID27127175
PMCPMC5078044
OpenAlexW2344755899

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.