Evidence map›Paper›PMID 30191636›Full record

ArticleCancer science2018

Inhibition of kinesin family member 20B sensitizes hepatocellular carcinoma cell to microtubule-targeting agents by blocking cytokinesis.

Xinran Liu, Yangkai Li, Xia Zhang, Xin-Yuan Liu, Anlin Peng, Yuchen Chen, Lijing Meng, Hong Chen, Yu Zhang, Xiaoping Miao and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2018. 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
1.5field-weighted citation impact, top 19% 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, 26 citations in OpenAlex.

  1. Article
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  5. The role of kinesin superfamily proteins in hepatocellular carcinoma.Medical oncology (Northwood, London, England) · 2024
    Review
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  9. Endothelial c-Myc knockout enhances diet-induced liver inflammation and fibrosis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
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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

12 authors at 6 institutions in 1 country.

Xinran LiuTongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan, China.
Yangkai LiTongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Xia ZhangTongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan, China.
Xin-Yuan LiuInstitute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Anlin PengThe Third Hospital of Wuhan, Wuhan, China.
Yuchen ChenTongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan, China.
Lijing MengTongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan, China.
Hong ChenTongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan, China.
Yu ZhangTongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan, China.
Xiaoping MiaoTongji School of Public Health, Huazhong University of Science and Technology, Wuhan, China.
Ling ZhengCollege of Life Sciences, Wuhan University, Wuhan, China.
Kun HuangTongji School of Pharmacy, Huazhong University of Science and Technology, Wuhan, China.ORCID http://orcid.org/0000-0002-0808-2325
Huazhong University of Science and Technology · CNChinese Academy of Sciences · CNTongji Hospital · CNWuhan Institute of Bioengineering · CNWuhan Third Hospital · CNWuhan University · CN

Funding

Academic Frontier Youth Team Project of HUST, Integrated Innovative Team for Major Human Diseases Program of Tongji Medical College (HUST)National Natural Science Foundation of China 31671195Natural Science Foundation of Hubei Province 2014CFA021Natural Science Foundation of Hubei Province 2017CFB651Natural Science Foundation of the Self-dependent Innovation of HUST 2016YXMS144
6 · The paper itself

Abstract

Kinesin family member 20B (KIF20B, also known as MPHOSPH1) is a kinesin protein that plays a critical role in cytokinesis. Previously, we and others have demonstrated the oncogenic role of KIF20B in several cancers; however, the exact mechanisms underlying its tumorigenic effects remain unclear. Herein, we showed overexpression of KIF20B in human hepatocellular carcinoma (HCC) and reported a negative correlation between KIF20B level and prognosis of patients. Mechanistically, reducing KIF20B blockades mitotic exit of HCC cells at telophase in a spindle assembly checkpoint independent way. Importantly, reducing KIF20B acts synergistically with three microtubule-associated agents (MTA) to p53- or p14ARF-dependently suppress p53-wt or p53-null HCC cells. In addition to taxol, reducing KIF20B also enhanced the toxicity of two chemotherapeutic drugs, hydroxycamptothecin and mitomycin C. In conclusion, we found a novel mechanism in that blocking cytokinesis by KIF20B inhibition increases the efficacy of MTA; our results thus suggested a dual-mitotic suppression approach against HCC by combining MTA with KIF20B inhibition, which simultaneously blocks mitosis at both metaphase and telophase.

Indexed as

Carcinoma, HepatocellularCell Line, TumorCell ProliferationCell SurvivalCytokinesisDrug SynergismGene Expression Regulation, NeoplasticHep G2 CellsHumansKinesinsLiver NeoplasmsMitosisPrognosisRNA, Small InterferingTubulin ModulatorsUp-RegulationKIF20B protein, humanKinesinsRNA, Small InterferingTubulin Modulatorscytokinesis defecthepatocellular carcinomaKIF20Bmetaphase and telophase inhibitionmicrotubule-targeting agent resistance

Identifiers

PMID30191636
PMCPMC6215872
OpenAlexW2891409588

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.