Evidence map›Paper›PMID 30206215›Full record

ArticleOncogenesis2018

TTK promotes mesenchymal signaling via multiple mechanisms in triple negative breast cancer.

Jamie L King, Baotong Zhang, Yixiang Li, Kathy P Li, Jianping J Ni, Harold I Saavedra, Jin-Tang Dong

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Developing a gene expression classifier for breast cancer diagnosis.Medical & biological engineering & computing · 2025
    Article
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  5. Identification of Associations with Dermatologic Diseases through a Focused GWAS of the UK Biobank.JID innovations : skin science from molecules to population health · 2025
    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

7 authors at 2 institutions in 2 countries.

Jamie L KingWinship Cancer Institute, Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Baotong ZhangWinship Cancer Institute, Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Yixiang LiWinship Cancer Institute, Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Kathy P LiWinship Cancer Institute, Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Jianping J NiWinship Cancer Institute, Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.
Harold I SaavedraDepartment of Pharmacology, Ponce Health Sciences University School of Medicine, Ponce Research Institute, Ponce, Puerto Rico. hsaavedra@psm.edu.
Jin-Tang DongWinship Cancer Institute, Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA. j.dong@emory.edu.ORCID http://orcid.org/0000-0003-2349-5782
Emory University · USPonce Health Sciences University · PR

Funding

Winship Cancer Institute Cancer Center Support GrantP30CA138292 · NCI · EMORY UNIVERSITY · PI Suresh S Ramalingam · 2009 to 2026
$47.5M
TECHNOLOGIES AND RESOURCES FOR CORE LABORATORIESU54MD007587 · NIMHD · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI LUCIANO, CARLOS A., WOJNA, VALERIE · 2012 to 2018
$23.2M
Using MC1R genotype to impact skin cancer risk behaviors in Hispanics/LatinosU54CA163068 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI KENNETH Lynn WRIGHT · 2012 to 2026
$23.1M
Using MC1R genotype to impact skin cancer risk behaviors in Hispanics/LatinosU54CA163071 · NCI · PONCE SCHOOL OF MEDICINE · PI Luisa Morales-Torres · 2012 to 2026
$23.0M
VIRAL SEQUENCES IN PEDIATRIC HIV INFECTION IN PRG12MD007579 · NIMHD · PONCE SCHOOL OF MEDICINE · PI TORRES-RUIZ, JOSE A · 2012 to 2018
$15.9M
Emory Initiative for Maximizing Student DevelopmentR25GM099644 · NIGMS · EMORY UNIVERSITY · PI MARSTELLER, PATRICIA A., WILKINSON, KEITH D · 2013 to 2017
$2.7M
Bidirectional role of KLF5 in prostatic epithelial homeostasis and tumorigenesisR01CA171189 · NCI · EMORY UNIVERSITY · PI DONG, JIN-TANG · 2013 to 2017
$1.6M
Nek2 and NPM in centrosome amplificationR01CA151521 · NCI · EMORY UNIVERSITY · PI SAAVEDRA, HAROLD I · 2010 to 2014
$1.5M
FUNCTIONAL ANALYSIS OF BRCA1 MUTANTSR01CA092309 · NCI · STRANG CANCER PREVENTION CENTER · PI MONTEIRO, ALVARO N · 2002 to 2006
$1.3M
NCI NIH HHS P30 CA138292NCI NIH HHS R01 CA092309NCI NIH HHS R01 CA151521NCI NIH HHS R01 CA171189NCI NIH HHS U54 CA163068NCI NIH HHS U54 CA163071NIGMS NIH HHS R25 GM099644NIMHD NIH HHS G12 MD007579NIMHD NIH HHS U54 MD007587
6 · The paper itself

Abstract

Abnormal expression of TTK kinase has been associated with the initiation, progression, and therapeutic resistance of breast and other cancers, but its roles remain to be clarified. In this study, we examined the role of TTK in triple negative breast cancer (TNBC), and found that higher TTK expression correlated with mesenchymal and proliferative phenotypes in TNBC cells. Pharmacologic inhibition and genomic silencing of TTK not only reversed the epithelial-to-mesenchymal transition (EMT) in TNBC cells, but also increased the expression of KLF5, an effector of TGF-β signaling and inhibitor of EMT. In addition, TTK inhibition decreased the expression of EMT-associated micro-RNA miR-21 but increased the expression of miR-200 family members and suppressed TGF-β signaling. To test if upregulation of KLF5 plays a role in TTK-induced EMT, TTK and KLF5 were silenced simultaneously, which reversed the decreased EMT caused by loss of TTK. Consistently, the decrease in miR-21 expression and increase in miR-200 expression caused by TTK silencing were rescued by loss of KLF5. Altogether, this study highlights a novel role and signaling pathway for TTK in regulating EMT of TN breast cancer cells through TGF-β and KLF5 signaling, highlighting targetable signaling pathways for TTK inhibitors in aggressive breast cancer.

Identifiers

PMID30206215
PMCPMC6133923
OpenAlexW2890897078

What OpenQuestion holds

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Registered trials

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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.