Evidence map›Paper›PMID 26148251›Full record

ArticleCell cycle (Georgetown, Tex.)2015

Functional analysis of phosphorylation of the mitotic centromere-associated kinesin by Aurora B kinase in human tumor cells.

Andreas Ritter, Mourad Sanhaji, Alexandra Friemel, Susanne Roth, Udo Rolle, Frank Louwen, Juping Yuan

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Andreas Rittera Department of Gynecology and Obstetrics ; JW Goethe-University ; Frankfurt , Germany.
Mourad Sanhajia Department of Gynecology and Obstetrics ; JW Goethe-University ; Frankfurt , Germany.
Alexandra Friemela Department of Gynecology and Obstetrics ; JW Goethe-University ; Frankfurt , Germany.
Susanne Rotha Department of Gynecology and Obstetrics ; JW Goethe-University ; Frankfurt , Germany.
Udo Rolleb Department of Pediatric Surgery and Pediatric Urology ; School of Medicine; JW Goethe-University ; Frankfurt , Germany.
Frank Louwena Department of Gynecology and Obstetrics ; JW Goethe-University ; Frankfurt , Germany.
Juping Yuana Department of Gynecology and Obstetrics ; JW Goethe-University ; Frankfurt , Germany.
Goethe University Frankfurt · DEGoethe Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitotic centromere-associated kinesin (MCAK) is the best characterized member of the kinesin-13 family and plays important roles in microtubule dynamics during mitosis. Its activity and subcellular localization is tightly regulated by an orchestra of mitotic kinases, such as Aurora B. It is well known that serine 196 of MCAK is the major phosphorylation site of Aurora B in Xenopus leavis extracts and that this phosphorylation regulates its catalytic activity and subcellular localization. In the current study, we have addressed the conserved phosphorylation site serine 192 in human MCAK to characterize its function in more depth in human cancer cells. Our data confirm that S192 is the major phosphorylation site of Aurora B in human MCAK and that this phosphorylation has crucial roles in regulating its catalytic activity and localization at the kinetochore/centromere region in mitosis. Interfering with this phosphorylation leads to a delayed progression through prometa- and metaphase associated with mitotic defects in chromosome alignment and segregation. We show further that MCAK is involved in directional migration and invasion of tumor cells, and interestingly, interference with the S192 phosphorylation affects this capability of MCAK. These data provide the first molecular explanation for clinical observation, where an overexpression of MCAK was associated with lymphatic invasion and lymph node metastasis in gastric and colorectal cancer patients.

Indexed as

Aurora Kinase BBinding SitesCell Line, TumorCell MovementHeLa CellsHumansKinesinsMitosisNeoplasm InvasivenessNeoplasm MetastasisPhosphorylationProtein Processing, Post-TranslationalProtein Structure, TertiaryAURKB protein, humanAurora Kinase BKIF2C protein, humanKinesinsAurora Bcell motilityMCAK phosphorylationmicrotubule dynamicsmitotic defect

Identifiers

PMID26148251
PMCPMC4825789
OpenAlexW2220986820

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.