Evidence map›Paper›PMID 25242325›Full record

ArticleCell reports2014

Structural insights into the tumor-promoting function of the MTDH-SND1 complex.

Feng Guo, Liling Wan, Aiping Zheng, Vitali Stanevich, Yong Wei, Kenneth A Satyshur, Minhong Shen, Woojong Lee, Yibin Kang, Yongna Xing

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

33 citing papers in PubMed, 53 citations in OpenAlex.

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  16. WTAP-mediated mCell death and differentiation · 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

10 authors at 2 institutions in 1 country.

Feng GuoMcArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI 53706, USA.
Liling WanDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Aiping ZhengMcArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI 53706, USA.
Vitali StanevichMcArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI 53706, USA.
Yong WeiDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Kenneth A SatyshurMcArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI 53706, USA.
Minhong ShenDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Woojong LeeMcArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI 53706, USA.
Yibin KangDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA. Electronic address: ykang@princeton.edu.
Yongna XingMcArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI 53706, USA. Electronic address: xing@oncology.wisc.edu.
University of Wisconsin–Madison · USPrinceton University · US

Funding

Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
Structural and Biochemical Insights into PP2A Holoenzyme BiogenesisR01GM096060 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI XING, YONGNA · 2012 to 2016
$1.7M
Metadherin in Metastasis and Chemoresistance of Breast CancerR01CA134519 · NCI · PRINCETON UNIVERSITY · PI KANG, YIBIN · 2008 to 2012
$1.6M
Analysis of mRNA splicing in plant hormone signalingF32GM069090 · NIGMS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI MOCKLER, TODD C · 2003 to 2005
$139k
NCATS NIH HHS UL1 TR000427NCATS NIH HHS UL1TR000427NCI NIH HHS R01 CA134519NCI NIH HHS R01CA134519NIGMS NIH HHS F32 GM069090NIGMS NIH HHS R01 GM096060NIGMS NIH HHS R01GM69090
6 · The paper itself

Abstract

Metadherin (MTDH) and Staphylococcal nuclease domain containing 1 (SND1) are overexpressed and interact in diverse cancer types. The structural mechanism of their interaction remains unclear. Here, we determined the high-resolution crystal structure of MTDH-SND1 complex, which reveals an 11-residue MTDH peptide motif occupying an extended protein groove between two SN domains (SN1/2), with two MTDH tryptophan residues nestled into two well-defined pockets in SND1. At the opposite side of the MTDH-SND1 binding interface, SND1 possesses long protruding arms and deep surface valleys that are prone to binding with other partners. Despite the simple binding mode, interactions at both tryptophan-binding pockets are important for MTDH and SND1's roles in breast cancer and for SND1 stability under stress. Our study reveals a unique mode of interaction with SN domains that dictates cancer-promoting activity and provides a structural basis for mechanistic understanding of MTDH-SND1-mediated signaling and for exploring therapeutic targeting of this complex.

Indexed as

AnimalsBinding SitesCell Adhesion MoleculesCell Line, TumorCrystallography, X-RayEndonucleasesHumansHydrogen BondingMembrane ProteinsMiceMolecular Dynamics SimulationMutagenesis, Site-DirectedNuclear ProteinsProtein BindingProtein Structure, TertiaryRecombinant Fusion ProteinsCell Adhesion MoleculesEndonucleasesMembrane ProteinsMTDH protein, humanNuclear ProteinsRecombinant Fusion ProteinsRNA-Binding ProteinsSND1 protein, human

Identifiers

PMID25242325
PMCPMC4309369
OpenAlexW2086207586

What OpenQuestion holds

Textmetadata
LicenceTDM
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.