Evidence map›Paper›PMID 34354264›Full record

ArticleNature nanotechnology2021

Intrinsic bioactivity of black phosphorus nanomaterials on mitotic centrosome destabilization through suppression of PLK1 kinase.

Ximing Shao, Zhihao Ding, Wenhua Zhou, Yanyan Li, Zhibin Li, Haodong Cui, Xian Lin, Guoli Cao, Binghua Cheng, Haiyan Sun and 16 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature nanotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 111 citations in OpenAlex.

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  20. Black Phosphorus Accelerates Bone Regeneration Based on Immunoregulation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    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

26 authors at 3 institutions in 2 countries.

Ximing Shao *Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Zhihao Ding *Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Wenhua ZhouShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Yanyan LiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Zhibin LiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Haodong CuiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Xian LinShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Guoli CaoShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Binghua ChengShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Haiyan SunShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Meiqing LiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Ke LiuShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Danyi LuShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.ORCID http://orcid.org/0000-0002-3346-2362
Shengyong GengShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Wenli ShiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Guofang ZhangShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Qingle SongShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Liang ChenShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Guocheng WangShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Wu SuShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Lintao CaiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.ORCID http://orcid.org/0000-0002-2461-6390
Lijing FangShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
David Tai LeongDepartment of Chemical and Biomolecular Engineering, National University of Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0001-8539-9062
Yang LiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China. yang.li@siat.ac.cn.ORCID http://orcid.org/0000-0001-7242-4687
Xue-Feng YuShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China. xf.yu@siat.ac.cn.ORCID http://orcid.org/0000-0003-2566-6194
Hongchang LiShenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China. hc.li@siat.ac.cn.ORCID http://orcid.org/0000-0003-0072-4706
Chinese Academy of Sciences · CNNational University of Singapore · SGShenzhen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although nanomaterials have shown promising biomedical application potential, incomplete understanding of their molecular interactions with biological systems prevents their inclusion into mainstream clinical applications. Here we show that black phosphorus (BP) nanomaterials directly affect the cell cycle's centrosome machinery. BP destabilizes mitotic centrosomes by attenuating the cohesion of pericentriolar material and consequently leads to centrosome fragmentation within mitosis. As a result, BP-treated cells exhibit multipolar spindles and mitotic delay, and ultimately undergo apoptosis. Mechanistically, BP compromises centrosome integrity by deactivating the centrosome kinase polo-like kinase 1 (PLK1). BP directly binds to PLK1, inducing its aggregation, decreasing its cytosolic mobility and eventually restricting its recruitment to centrosomes for activation. With this mechanism, BP nanomaterials show great anticancer potential in tumour xenografted mice. Together, our study reveals a molecular mechanism for the tumoricidal properties of BP and proposes a direction for biomedical application of nanomaterials by exploring their intrinsic bioactivities.

Indexed as

AnimalsApoptosisCell Cycle ProteinsCentrosomeHeLa CellsHeterograftsHumansMiceMitosisNanostructuresNeoplasmsPhosphorusPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsCell Cycle ProteinsPhosphorusPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene Proteins

Identifiers

PMID34354264
OpenAlexW3192433760

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.