Evidence map›Paper›PMID 35216080›Full record

ArticleInternational journal of molecular sciences2022

Lysophosphatidic Acid Promotes the Expansion of Cancer Stem Cells via TRPC3 Channels in Triple-Negative Breast Cancer.

Naoya Hirata, Shigeru Yamada, Shota Yanagida, Atsushi Ono, Yukuto Yasuhiko, Motohiro Nishida, Yasunari Kanda

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
1.6field-weighted citation impact, top 17% 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, 22 citations in OpenAlex.

  1. Review
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  4. The Mechanism of LTXInternational journal of molecular sciences · 2025
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  7. Calcium channels as pharmacological targets for cancer therapy.Clinical and experimental medicine · 2025
    Review
  8. Review
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  10. Article
  11. Review
  12. Review
  13. Crosstalk between CaInternational journal of molecular sciences · 2022
    Review
  14. Article
  15. Review
  16. Article
  17. 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

7 authors at 3 institutions in 1 country.

Naoya HirataDivision of Pharmacology, National Institute of Health Sciences, Kanagawa 210-9501, Japan.
Shigeru YamadaDivision of Pharmacology, National Institute of Health Sciences, Kanagawa 210-9501, Japan.
Shota YanagidaDivision of Pharmacology, National Institute of Health Sciences, Kanagawa 210-9501, Japan.
Atsushi OnoDivision of Pharmaceutical Sciences, Graduated School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama 700-8530, Japan.ORCID 0000-0001-5056-0442
Yukuto YasuhikoDivision of Pharmacology, National Institute of Health Sciences, Kanagawa 210-9501, Japan.ORCID 0000-0002-1366-0978
Motohiro NishidaGraduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka 812-8582, Japan.ORCID 0000-0002-2587-5458
Yasunari KandaDivision of Pharmacology, National Institute of Health Sciences, Kanagawa 210-9501, Japan.ORCID 0000-0003-2527-3526
National Institute of Health Sciences · JPOkayama University · JPKyushu University · JP

Funding

Japan Agency for Medical Research and Development JP21mk0101189Ministry of Education, Culture, Sports, Science and Technology #17H04107Ministry of Education, Culture, Sports, Science and Technology #17K15586Ministry of Education, Culture, Sports, Science and Technology #21H02634
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is a highly aggressive cancer for which targeted therapeutic agents are limited. Growing evidence suggests that TNBC originates from breast cancer stem cells (BCSCs), and elucidation of the molecular mechanisms controlling BCSC proliferation will be crucial for new drug development. We have previously reported that the lysosphingolipid sphingosine-1-phosphate mediates the CSC phenotype, which can be identified as the ALDH-positive cell population in several types of human cancer cell lines. In this study, we have investigated additional lipid receptors upregulated in BCSCs. We found that lysophosphatidic acid (LPA) receptor 3 was highly expressed in ALDH-positive TNBC cells. The LPAR3 antagonist inhibited the increase in ALDH-positive cells after LPA treatment. Mechanistically, the LPA-induced increase in ALDH-positive cells was dependent on intracellular calcium ion (Ca

Indexed as

BreastCalciumCell Line, TumorEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansInterleukin-8LysophospholipidsNeoplastic Stem CellsReceptors, Lysophosphatidic AcidSignal TransductionSphingosineTriple Negative Breast NeoplasmsTRPC Cation ChannelsCalciumInterleukin-8lysophosphatidic acidLysophospholipidsReceptors, Lysophosphatidic AcidSphingosinesphingosine 1-phosphateTRPC3 cation channelTRPC Cation Channelscancer stem cellslysophosphatidic acidnuclear factor of activated T cellstransient receptor potential cation channel subfamily C member 3triple-negative breast cancer

Identifiers

PMID35216080
PMCPMC8877950
OpenAlexW4211160157

What Socratic 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 Socratic graph.