Evidence map›Paper›PMID 25689426›Full record

ReviewInternational journal of molecular sciences2015

Autophagy as a regulatory component of erythropoiesis.

Jieying Zhang, Kunlu Wu, Xiaojuan Xiao, Jiling Liao, Qikang Hu, Huiyong Chen, Jing Liu, Xiuli An

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.7field-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

45 citing papers in PubMed, 66 citations in OpenAlex.

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  16. Reticulocyte Maturation.Membranes · 2022
    Review
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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

8 authors at 2 institutions in 2 countries.

Jieying ZhangState Key Laboratory of Medical Genetics & School of Life Sciences, Central South University, Changsha 410078, China. jzhang@nybloodcenter.org.
Kunlu WuState Key Laboratory of Medical Genetics & School of Life Sciences, Central South University, Changsha 410078, China. wukunlu@163.com.
Xiaojuan XiaoState Key Laboratory of Medical Genetics & School of Life Sciences, Central South University, Changsha 410078, China. xiaojuan_xiao0809@163.com.
Jiling LiaoState Key Laboratory of Medical Genetics & School of Life Sciences, Central South University, Changsha 410078, China. liaojilingcsu@163.com.
Qikang HuState Key Laboratory of Medical Genetics & School of Life Sciences, Central South University, Changsha 410078, China. huqikang1001@163.com.
Huiyong ChenState Key Laboratory of Medical Genetics & School of Life Sciences, Central South University, Changsha 410078, China. chenhy5000@126.com.
Jing LiuState Key Laboratory of Medical Genetics & School of Life Sciences, Central South University, Changsha 410078, China. liaojilingcsu@163.com.
Xiuli AnLaboratory of Membrane Biology, New York Blood Center, New York, NY 10065, USA. xan@nybloodcenter.org.
Central South University · CNNew York Blood Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a process that leads to the degradation of unnecessary or dysfunctional cellular components and long-lived protein aggregates. Erythropoiesis is a branch of hematopoietic differentiation by which mature red blood cells (RBCs) are generated from multi-potential hematopoietic stem cells (HSCs). Autophagy plays a critical role in the elimination of mitochondria, ribosomes and other organelles during erythroid terminal differentiation. Here, the modulators of autophagy that regulate erythroid differentiation were summarized, including autophagy-related (Atg) genes, the B-cell lymphoma 2 (Bcl-2) family member Bcl-2/adenovirus E1B 19 kDa interacting protein 3-like (Nix/Binp3L), transcription factors globin transcription factor 1 (GATA1) and forkhead box O3 (FoxO3), intermediary factor KRAB-associated protein1 (KAP1), and other modulators, such as focal adhesion kinase family-interacting protein of 200-kDa (FIP200), Ca2+ and 15-lipoxygenase. Understanding the modulators of autophagy in erythropoiesis will benefit the autophagy research field and facilitate the prevention and treatment of autophagy-related red blood cell disorders.

Indexed as

AutophagyErythropoiesisArachidonate 15-Lipoxygenasebeta-ThalassemiaErythrocytesHematopoietic Stem CellsHumansProtein-Tyrosine KinasesProto-Oncogene Proteins c-bcl-2Transcription FactorsArachidonate 15-LipoxygenaseProtein-Tyrosine KinasesProto-Oncogene Proteins c-bcl-2Transcription Factors

Identifiers

PMID25689426
PMCPMC4346945
OpenAlexW2084988418

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.