Evidence map›Paper›PMID 29926310›Full record

ReviewCancer metastasis reviews2018

Role of autotaxin in cancer stem cells.

Dongjun Lee, Dong-Soo Suh, Sue Chin Lee, Gabor J Tigyi, Jae Ho Kim

Abstract readReview
In one paragraph

Review in Cancer metastasis reviews, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. E2F7 drives autotaxin/Enpp2 transcription via chromosome looping: Repression by p53 in murine but not in human carcinomas.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  10. Article
  11. Article
  12. Designing Dual Inhibitors of Autotaxin-LPAR GPCR Axis.Molecules (Basel, Switzerland) · 2022
    Review
  13. Article
  14. Observational
  15. Article
  16. Article
  17. Autotaxin: An Early Warning Biomarker for Acute-on-chronic Liver Failure.Journal of clinical and translational hepatology · 2020
    Article
  18. The Role of Lysophosphatidic Acid in Adult Stem Cells.International journal of stem cells · 2020
    Review
  19. Review
  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

5 authors at 2 institutions in 2 countries.

Dongjun LeeDepartment of Medical Science, Pusan National University School of Medicine, Yangsan, 50612, South Korea.
Dong-Soo SuhDepartment of Obstetrics and Gynecology, Pusan National University School of Medicine, Yangsan, 50612, South Korea.
Sue Chin LeeDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Gabor J TigyiDepartment of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Jae Ho KimDepartment of Physiology, Pusan National University School of Medicine, Yangsan, 50612, Gyeongsangnam-do, Republic of Korea. jhkimst@pusan.ac.kr.
Pusan National University · KRUniversity of Tennessee Health Science Center · 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
Analysis of Radiomitigative Cell SignalingR01AI080405 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI TIGYI, GABOR J · 2008 to 2012
$2.1M
Novel Radiomitigators Targeting LPA ReceptorsI01BX001187 · VA · MEMPHIS VA MEDICAL CENTER · PI TIGYI, GABOR J · 2013 to 2016
–
BLRD VA I01 BX001187NCI NIH HHS R01 CA092160NIAID NIH HHS R01 AI080405
6 · The paper itself

Abstract

Stem cells are a rare subpopulation defined by the potential to self-renew and differentiate into specific cell types. A population of stem-like cells has been reported to possess the ability of self-renewal, invasion, metastasis, and engraftment of distant tissues. This unique cell subpopulation has been designated as cancer stem cells (CSC). CSC were first identified in leukemia, and the contributions of CSC to cancer progression have been reported in many different types of cancers. The cancer stem cell hypothesis attempts to explain tumor cell heterogeneity based on the existence of stem cell-like cells within solid tumors. The elimination of CSC is challenging for most human cancer types due to their heightened genetic instability and increased drug resistance. To combat these inherent abilities of CSC, multi-pronged strategies aimed at multiple aspects of CSC biology are increasingly being recognized as essential for a cure. One of the most challenging aspects of cancer biology is overcoming the chemotherapeutic resistance in CSC. Here, we provide an overview of autotaxin (ATX), lysophosphatidic acid (LPA), and their signaling pathways in CSC. Increasing evidence supports the role of ATX and LPA in cancer progression, metastasis, and therapeutic resistance. Several studies have demonstrated the ATX-LPA axis signaling in different cancers. This lipid mediator regulatory system is a novel potential therapeutic target in CSC. In this review, we summarize the evidence linking ATX-LPA signaling to CSC and its impact on cancer progression and metastasis. We also provide evidence for the efficacy of cancer therapy involving the pharmacological inhibition of this signaling pathway.

Indexed as

AnimalsHumansLysophospholipase DLysophospholipidsNeoplasmsNeoplastic Stem CellsPhosphoric Diester Hydrolaseslysophosphatidic acidLysophospholipase DLysophospholipidsPhosphoric Diester HydrolasesAutotaxinCancer stem cellsLysophosphatidic acidLysophosphatidic acid receptor

Identifiers

PMID29926310
PMCPMC6309296
OpenAlexW2808846255

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.