Evidence map›Paper›PMID 25158955›Full record

ArticleMolecular cancer research : MCR2015

Autotaxin and LPA1 and LPA5 receptors exert disparate functions in tumor cells versus the host tissue microenvironment in melanoma invasion and metastasis.

Sue-Chin Lee, Yuko Fujiwara, Jianxiong Liu, Junming Yue, Yoshibumi Shimizu, Derek D Norman, Yaohong Wang, Ryoko Tsukahara, Erzsebet Szabo, Renukadevi Patil and 7 more

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

55 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. PARP1 modulates METTL3 promoter chromatin accessibility and associated LPAR5 RNA mMolecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Designing Dual Inhibitors of Autotaxin-LPAR GPCR Axis.Molecules (Basel, Switzerland) · 2022
    Review
  10. World journal of gastrointestinal oncology · 2022
    Review
  11. Article
  12. Review
  13. Article
  14. Revisiting the role of lysophosphatidic acid in stem cell biology.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  15. Article
  16. Review
  17. LPACells · 2021
    Article
  18. 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

17 authors at 2 institutions in 1 country.

Sue-Chin LeeDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Yuko FujiwaraDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Jianxiong LiuDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Junming YueDepartment of Pathology, University of Tennessee Health Science Center, Memphis, Tennessee.
Yoshibumi ShimizuDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Derek D NormanDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Yaohong WangDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Ryoko TsukaharaDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Erzsebet SzaboDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Renukadevi PatilDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, Tennessee.
Souvik BanerjeeDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, Tennessee.
Duane D MillerDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Tennessee Health Science Center, Memphis, Tennessee.
Louisa BalazsDepartment of Pathology, University of Tennessee Health Science Center, Memphis, Tennessee.
Manik C GhoshDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Christopher M WatersDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee.
Tamas OraveczImmunology and Oncology, Lexicon Pharmaceuticals, The Woodlands, Texas.
Gabor J TigyiDepartment of Physiology, College of Medicine, University of Tennessee Health Science Center, Memphis, Tennessee. gtigyi@uthsc.edu.
University of Tennessee Health Science Center · USLexicon Pharmaceuticals (United States) · US

Funding

Ligand Recognition by Phospholipid Growth Factor ReceptorsR01CA092160 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TIGYI, GABOR J · 2001 to 2022
$5.9M
NCI NIH HHS CA 092160NCI NIH HHS R01 CA092160
6 · The paper itself

Abstract

unlabelledAutotaxin (ENPP2/ATX) and lysophosphatidic acid (LPA) receptors represent two key players in regulating cancer progression. The present study sought to understand the mechanistic role of LPA G protein-coupled receptors (GPCR), not only in the tumor cells but also in stromal cells of the tumor microenvironment. B16F10 melanoma cells predominantly express LPA5 and LPA2 receptors but lack LPA1. LPA dose dependently inhibited invasion of cells across a Matrigel layer. RNAi-mediated knockdown of LPA5 relieved the inhibitory effect of LPA on invasion without affecting basal invasion. This suggests that LPA5 exerts an anti-invasive action in melanoma cells in response to LPA. In addition, both siRNA-mediated knockdown and pharmacologic inhibition of LPA2 reduced the basal rate invasion. Unexpectedly, when probing the role of this GPCR in host tissues, it was found that the incidence of melanoma-derived lung metastasis was greatly reduced in LPA5 knockout (KO) mice compared with wild-type (WT) mice. LPA1-KO but not LPA2-KO mice also showed diminished melanoma-derived lung metastasis, suggesting that host LPA1 and LPA5 receptors play critical roles in the seeding of metastasis. The decrease in tumor cell residence in the lungs of LPA1-KO and LPA5-KO animals was apparent 24 hours after injection. However, KO of LPA1, LPA2, or LPA5 did not affect the subcutaneous growth of melanoma tumors. IMPLICATIONS: These findings suggest that tumor and stromal LPA receptors, in particular LPA1 and LPA5, play different roles in invasion and the seeding of metastasis.

Indexed as

AnimalsCarcinogenesisHumansLung NeoplasmsLysophospholipase DMelanoma, ExperimentalMiceMice, KnockoutNeoplasm InvasivenessNeoplasm MetastasisPhosphoric Diester HydrolasesReceptors, Lysophosphatidic AcidSignal TransductionTumor MicroenvironmentLPAR5 protein, mouseLysophospholipase DPhosphoric Diester HydrolasesReceptors, Lysophosphatidic Acid

Identifiers

PMID25158955
PMCPMC4297753
OpenAlexW1990390822

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.