Evidence map›Paper›PMID 29880710›Full record

ArticleEMBO reports2018

Map7/7D1 and Dvl form a feedback loop that facilitates microtubule remodeling and Wnt5a signaling.

Koji Kikuchi, Akira Nakamura, Masaki Arata, Dongbo Shi, Mami Nakagawa, Tsubasa Tanaka, Tadashi Uemura, Toshihiko Fujimori, Akira Kikuchi, Akiyoshi Uezu and 2 more

Open access · greenAbstract read
In one paragraph

Article in EMBO reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  14. Wnt5a Signaling in Gastric Cancer.Frontiers in cell and developmental biology · 2020
    Review
  15. Article
  16. Article
  17. Regulation of Proliferation and Epithelial-to-Mesenchymal Transition (EMT) of Gastric Cancer by ZEB1 via Modulating Wnt5a and Related Mechanisms.Medical science monitor : international medical journal of experimental and clinical research · 2019
    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

12 authors at 4 institutions in 1 country.

Koji KikuchiDepartment of Molecular Pharmacology, Graduate School of Medical Sciences, Kumamoto University, Chuo-ku Kumamoto, Japan kojik@kumamoto-u.ac.jp hnakanis@gpo.kumamoto-u.ac.jp.ORCID 0000-0002-7616-8200
Akira NakamuraDepartment of Germline Development, Institute of Molecular Embryology and Genetics, Kumamoto University, Chuo-ku Kumamoto, Japan.
Masaki ArataGraduate School of Biostudies, Kyoto University, Sakyo-ku Kyoto, Japan.
Dongbo ShiDivision of Embryology, National Institute for Basic Biology, Okazaki Aichi, Japan.ORCID 0000-0002-4408-3042
Mami NakagawaDivision of Embryology, National Institute for Basic Biology, Okazaki Aichi, Japan.
Tsubasa TanakaDepartment of Germline Development, Institute of Molecular Embryology and Genetics, Kumamoto University, Chuo-ku Kumamoto, Japan.
Tadashi UemuraGraduate School of Biostudies, Kyoto University, Sakyo-ku Kyoto, Japan.
Toshihiko FujimoriDivision of Embryology, National Institute for Basic Biology, Okazaki Aichi, Japan.
Akira KikuchiDepartment of Molecular Biology and Biochemistry, Graduate School of Medicine, Osaka University, Suita Osaka, Japan.
Akiyoshi UezuDepartment of Molecular Pharmacology, Graduate School of Medical Sciences, Kumamoto University, Chuo-ku Kumamoto, Japan.
Yasuhisa SakamotoDepartment of Molecular Pharmacology, Graduate School of Medical Sciences, Kumamoto University, Chuo-ku Kumamoto, Japan.
Hiroyuki NakanishiDepartment of Molecular Pharmacology, Graduate School of Medical Sciences, Kumamoto University, Chuo-ku Kumamoto, Japan kojik@kumamoto-u.ac.jp hnakanis@gpo.kumamoto-u.ac.jp.ORCID 0000-0002-9765-0266
Kumamoto University · JPNational Institute for Basic Biology · JPKyoto University · JPThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Wnt signaling pathway can be grouped into two classes, the β-catenin-dependent and β-catenin-independent pathways. Wnt5a signaling through a β-catenin-independent pathway promotes microtubule (MT) remodeling during cell-substrate adhesion, cell migration, and planar cell polarity formation. Although Wnt5a signaling and MT remodeling are known to form an interdependent regulatory loop, the underlying mechanism remains unknown. Here we show that in HeLa cells, the paralogous MT-associated proteins Map7 and Map7D1 (Map7/7D1) form an interdependent regulatory loop with Disheveled, the critical signal transducer in Wnt signaling. Map7/7D1 bind to Disheveled, direct its cortical localization, and facilitate the cortical targeting of MT plus-ends in response to Wnt5a signaling. Wnt5a signaling also promotes Map7/7D1 movement toward MT plus-ends, and depletion of the Kinesin-1 member Kif5b abolishes the Map7/7D1 dynamics and Disheveled localization. Furthermore, Disheveled stabilizes Map7/7D1. Intriguingly, Map7/7D1 and its

Indexed as

Evolution, MolecularAnimalsbeta CateninCell MovementCell PolarityDishevelled ProteinsDrosophilaHeLa CellsHumansKinesinsMiceMicrotubule-Associated ProteinsProtein BindingWnt-5a ProteinWnt Signaling Pathwaybeta CateninCTNNB1 protein, humanDishevelled ProteinsDVL1 protein, humanKIF5B protein, humanKinesinsMicrotubule-Associated ProteinsWnt-5a ProteinWNT5A protein, humanDisheveledKinesin‐1microtubule‐associated proteinsmicrotubule remodelingβ‐catenin‐independent Wnt5a signaling

Identifiers

PMID29880710
PMCPMC6030700
OpenAlexW2805880543

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.