Evidence map›Paper›PMID 28687976›Full record

ArticleFrontiers of medicine2017

Annexin A2-S100A10 heterotetramer is upregulated by PML/RARα fusion protein and promotes plasminogen-dependent fibrinolysis and matrix invasion in acute promyelocytic leukemia.

Dan Huang, Yan Yang, Jian Sun, Xiaorong Dong, Jiao Wang, Hongchen Liu, Chengquan Lu, Xueyu Chen, Jing Shao, Jinsong Yan

Abstract read
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Article in Frontiers of medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Dysregulated hemostasis in acute promyelocytic leukemia.International journal of hematology · 2024
    Review
  3. Article
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  18. S100 Proteins in Acute Myeloid Leukemia.Neoplasia (New York, N.Y.) · 2018
    Review
  19. 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

10 authors at 2 institutions in 1 country.

Dan HuangDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Hematology of the Second Hospital of Dalian Medical University, Dalian, 116027, China.
Yan YangDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Hematology of the Second Hospital of Dalian Medical University, Dalian, 116027, China.
Jian SunDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Hematology of the Second Hospital of Dalian Medical University, Dalian, 116027, China.
Xiaorong DongDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Hematology of the Second Hospital of Dalian Medical University, Dalian, 116027, China.
Jiao WangDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Hematology of the Second Hospital of Dalian Medical University, Dalian, 116027, China.
Hongchen LiuDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Hematology of the Second Hospital of Dalian Medical University, Dalian, 116027, China.
Chengquan LuDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Environmental Health and Toxicology, School of Public Health, Dalian Medical University, Dalian, 116044, China.
Xueyu ChenDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Hematology of the Second Hospital of Dalian Medical University, Dalian, 116027, China.
Jing ShaoDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Environmental Health and Toxicology, School of Public Health, Dalian Medical University, Dalian, 116044, China. jshao@uw.edu.
Jinsong YanDalian Key Laboratory of Hematology, Liaoning Hematopoietic Stem Cell Transplantation Medical Center, Department of Hematology of the Second Hospital of Dalian Medical University, Dalian, 116027, China. yanjsdmu@126.com.
Dalian Medical University · CNSecond Affiliated Hospital of Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant expression of annexin A2-S100A10 heterotetramer (AIIt) associated with PML/RARα fusion protein causes lethal hyperfibrinolysis in acute promyelocytic leukemia (APL), but the mechanism is unclear. To facilitate the investigation of regulatory association between ANXA2 and promyelocytic leukemia/retinoic acid receptor a (PML/RARα) fusion protein, this work was performed to determine the transcription start site of ANXA2 promoter with rapid amplification of 5'-cDNA ends analysis. Zinc-induced U937/PR9 cells expressed PML/RARα fusion protein, and resultant increases in ANXA2 transcripts and translational expressions of both ANXA2 and S100A10, while S100A10 transcripts remained constitutive. The transactivation of ANXA2 promoter by PML/RARα fusion protein was 3.29 ± 0.13 fold higher than that by control pSG5 vector or wild-type RARα. The overexpression of ANXA2 in U937 transfected with full-length ANXA2 cDNA was associated with increased S100A10 subunit, although S100A10 transcripts remained constitutive. The tPA-dependent initial rate of plasmin generation (IRPG) in zinc-treated U937/PR9 increased by 2.13-fold, and cell invasiveness increased by 27.6%. Antibodies against ANXA2, S100A10, or combination of both all remarkably inhibited the IRPG and invasiveness in U937/PR9 and NB4. Treatment of zinc-induced U937/PR9 or circulating APL blasts with all-trans retinoic acid (ATRA) significantly reduced cell surface ANXA2 and S100A10 and associated reductions in IRPG and invasiveness. Thus, PML/RARα fusion protein transactivated the ANXA2 promoter to upregulate ANXA2 and accumulate S100A10. Increased AIIt promoted IRPG and invasiveness, both of which were partly abolished by antibodies against ANXA2 and S100A10 or by ATRA.

Indexed as

Annexin A2FibrinolysisHumansLeukemia, Promyelocytic, AcuteNuclear ProteinsOncogene Proteins, FusionPlasminogenS100 Calcium Binding Protein A10S100 ProteinsTranscription FactorsTretinoinTumor Cells, CulturedU937 CellsAnnexin A2Nuclear ProteinsOncogene Proteins, FusionPlasminogenpromyelocytic leukemia-retinoic acid receptor alpha fusion oncoproteinS100 Calcium Binding Protein A10S100 ProteinsTranscription FactorsTretinoinacute promyelocytic leukemiaannexin A2-S100A10 heterotetramercell invasionplasminPML/RARα fusion protein

Identifiers

PMID28687976
OpenAlexW2734273643

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.