Evidence map›Paper›PMID 31370073›Full record

ArticleThrombosis and haemostasis2019

All-Trans Retinoic Acid Impairs Platelet Function and Thrombus Formation and Inhibits Protein Kinase CßI/δ Phosphorylation.

Qi Luo, Guangyu Wei, Xiamin Wang, Xiaoqi Xu, Wen Ju, Zhenyu Li, Elizabeth E Gardiner, Robert K Andrews, Lingyu Zeng, Kailin Xu and 1 more

Erratum issuedAbstract read
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In one paragraph

Article in Thrombosis and haemostasis, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Systemic Review of Clot Retraction Modulators.International journal of molecular sciences · 2023
    Pooled it
  2. Article
  3. Article
  4. Effect of Therapeutically Related Drugs on Coagulation-Anticoagulation Balance in Acute Promyelocytic Leukemia.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Qi Luo *Blood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Guangyu Wei *Blood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Xiamin Wang *Blood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Xiaoqi XuBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Wen JuBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Zhenyu LiBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Elizabeth E GardinerACRF Department of Cancer Biology and Therapeutics, John Curtin School of Medical Research, The Australian National University, Canberra, Australia.ORCID 0000-0001-9453-9688
Robert K AndrewsAustralian Centre for Blood Diseases, Monash University, Melbourne, Australia.
Lingyu ZengBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Kailin XuBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Jianlin QiaoBlood Diseases Institute, Xuzhou Medical University, Xuzhou, China.
Xuzhou Medical College · CNAustralian Centre for HIV and Hepatitis Virology Research · AUAustralian National University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

All-trans retinoic acid (ATRA) is widely used for induction of complete remission in patients with acute promyelocytic leukemia (APL). ATRA also regulates protein kinase C (PKC) activity. Therapeutic use of ATRA reportedly interferes with hemostatic function in APL patients, including effects on coagulation or other vascular cells, although effects of ATRA on platelets remain unclear. This study aims to investigate the effect of therapeutic-relevant doses of ATRA on platelet function. Human platelets were preincubated with ATRA (0-20 μM) for 1 hour at 37°C, followed by analysis of aggregation, granule secretion, receptor expression by flow cytometry, platelet spreading, or clot retraction. Additionally, ATRA (10 mg/kg) was injected intraperitoneally into mice and tail bleeding time and arterial thrombus formation were evaluated. ATRA inhibited platelet aggregation and adenosine triphosphate release induced by collagen (5 μg/mL) or thrombin (0.05 U/mL) in a dose-dependent manner without affecting P-selectin expression or surface levels of glycoprotein (GP) Ibα, GPVI, or α

Indexed as

AnimalsBlood CoagulationBlood PlateletsCardiovascular DiseasesClot RetractionCollagenCytoskeletonHemostasisHumansMiceMice, Inbred C57BLPhosphorylationPlatelet ActivationPlatelet AggregationPlatelet Function TestsProtein Kinase C betaCollagenProtein Kinase C betaProtein Kinase C-deltaTretinoin

Identifiers

PMID31370073
OpenAlexW2966328233

What OpenQuestion holds

Textmetadata
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.