Evidence map›Paper›PMID 31212704›Full record

ReviewInternational journal of molecular sciences2019

Lysophosphatidic Acid Signaling in Diabetic Nephropathy.

Jong Han Lee, Donghee Kim, Yoon Sin Oh, Hee-Sook Jun

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 64 citations in OpenAlex.

  1. Trial
  2. Context-dependent lysophosphatidic acid signalling in inflammation: evidence hierarchy, myeloid regulation and translational gaps.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  3. Lysophosphatidic Acid Synergizes With 1,25-Dihydroxyvitamin D to Promote Fibroblast Growth Factor-23 Synthesis via MAPK Signaling and Induction of the IL12A Gene.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Investigation into temporal changes in the human bloodstain lipidome.International journal of legal medicine · 2025
    Article
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  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Glucagon-like Peptide-1 Secretion Is Inhibited by Lysophosphatidic Acid.International journal of molecular sciences · 2022
    Article
  20. 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 2 institutions in 1 country.

Jong Han LeeCollege of Pharmacy, Gachon University, Incheon 21936, Korea. jhleecw@gachon.ac.kr.
Donghee KimLee Gil Ya Cancer and Diabetes Institute, Gachon University, Incheon 21999, Korea. dh2388@gachon.ac.kr.
Yoon Sin OhDepartment of Food and Nutrition, Eulji University, Seongnam 13135, Korea. ysoh@eulji.ac.kr.ORCID 0000-0003-3995-4429
Hee-Sook JunCollege of Pharmacy, Gachon University, Incheon 21936, Korea. hsjun@gachon.ac.kr.ORCID 0000-0002-1166-4932
Gachon University · KREulji University · KR

Funding

Ministry of Education of Korea, The Ministry of Health & Welfare,Republic of Korea NRF-2016R1A2B2013347, NRF-2018R1C1B6000998, 2017R1D1A1B03036210, HI14C1135
6 · The paper itself

Abstract

Lysophosphatidic acid (LPA) is a bioactive phospholipid present in most tissues and body fluids. LPA acts through specific LPA receptors (LPAR1 to LPAR6) coupled with G protein. LPA binds to receptors and activates multiple cellular signaling pathways, subsequently exerting various biological functions, such as cell proliferation, migration, and apoptosis. LPA also induces cell damage through complex overlapping pathways, including the generation of reactive oxygen species, inflammatory cytokines, and fibrosis. Several reports indicate that the LPA-LPAR axis plays an important role in various diseases, including kidney disease, lung fibrosis, and cancer. Diabetic nephropathy (DN) is one of the most common diabetic complications and the main risk factor for chronic kidney diseases, which mostly progress to end-stage renal disease. There is also growing evidence indicating that the LPA-LPAR axis also plays an important role in inducing pathological alterations of cell structure and function in the kidneys. In this review, we will discuss key mediators or signaling pathways activated by LPA and summarize recent research findings associated with DN.

Indexed as

AnimalsDiabetic NephropathiesHumansLysophospholipidsRenal Insufficiency, ChronicSignal Transductionlysophosphatidic acidLysophospholipidschronic kidney injurydiabetic nephropathylysophosphatidic acidlysophosphatidic acid receptor

Identifiers

PMID31212704
PMCPMC6600156
OpenAlexW2950345003

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.