Evidence map›Paper›PMID 35831551›Full record

ArticleScientific reports2022

Proteomic profiling of plasma exosomes from patients with B-cell acute lymphoblastic leukemia.

Shicong Zhu, Cheng Xing, Ruijuan Li, Zhao Cheng, Mingyang Deng, Yunya Luo, Heng Li, Guangsen Zhang, Yue Sheng, Hongling Peng and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
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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

11 authors at 2 institutions in 1 country.

Shicong ZhuDepartment of Geriatrics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Cheng XingDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Ruijuan LiDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zhao ChengDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Mingyang DengDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yunya LuoDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Heng LiDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Guangsen ZhangDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yue ShengDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hongling PengDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zhihua WangDepartment of Hematology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China. wangzhihuazsc@csu.edu.cn.
Second Xiangya Hospital of Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to comprehensively investigate the proteomic profile and underlying biological function of exosomal proteins associated with B-cell acute lymphoblastic leukemia. Exosomes were isolated from plasma samples collected from five patients with B-ALL and five healthy individuals, and their protein content was quantitatively analyzed by liquid chromatography with tandem mass spectrometry. A total of 342 differentially expressed proteins were identified in patients with B-ALL. The DEPs were mainly associated with protein metabolic processes and protein activity regulation and were significantly enriched in the Notch and autophagy pathways. Furthermore, we found that ADAM17 and ATG3 were upregulated in patients with B-ALL and enriched in the Notch and autophagy pathways, respectively. Further western blot analysis of exosomes collected from additional 18 patients with B-ALL and 10 healthy controls confirmed that both ADAM17 and ATG3 were overexpressed in exosomes derived from patients with B-ALL (p < 0.001). The areas under the curves of ADAM17 and ATG3 were 0.989 and 0.956, respectively, demonstrating their diagnostic potential. In conclusion, ADAM17 and ATG3 in plasma-derived exosomes may contribute to the progression of B-ALL by regulating the Notch and autophagy pathways. Hence, these proteins may represent valuable diagnostic biomarkers and therapeutic targets for B-ALL.

Indexed as

ExosomesPrecursor Cell Lymphoblastic Leukemia-LymphomaChromatography, LiquidHumansProteomicsTandem Mass Spectrometry

Identifiers

PMID35831551
PMCPMC9279438
OpenAlexW4285392934

What OpenQuestion holds

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LicenceCC BY
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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.