Overexpressed DAAM1 correlates with metastasis and predicts poor prognosis in breast cancer.


Journal

Pathology, research and practice
ISSN: 1618-0631
Titre abrégé: Pathol Res Pract
Pays: Germany
ID NLM: 7806109

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 09 09 2019
revised: 26 10 2019
accepted: 10 11 2019
pubmed: 24 11 2019
medline: 20 11 2020
entrez: 24 11 2019
Statut: ppublish

Résumé

Recent studies have reported that dishevelled-associated activator of morphogenesis 1 (DAAM1) is remarkably essential for mediating cell migration and invasion in breast cancer (BrCa). Nonetheless, the definite expression profile of DAAM1 in BrCa patients and the impact on metastasis of BrCa in vivo have not been explored up to now. The differential expression of DAAM1 in BrCa and adjacent tissues was assessed via immunohistochemistry (IHC) staining. The metastatic capacities of BrCa SUM-1315 cells were examined in BALB/c nude mice. Besides, the prognostic values of DAAM1 mRNA in BrCa were explored based on Kaplan-Meier (KM) plotter. The expression of DAAM1 protein was notably overexpressed in BrCa tissues compared with that in paired normal breast tissues. The high expression of DAAM1 in BrCa tissues was significantly associated with lymph-node metastasis. Furthermore, DAAM1 overexpression promoted the invasive capacity of BrCa cells and stimulated lung metastatic extent in vivo. We also found that overexpressed DAAM1 mRNA was significantly associated with poor relapse-free survival (RFS), overall survival (OS), distance-metastasis-free survival (DMFS), and post-progression survival (PPS). Our findings reveal that DAAM1 might be a novel therapeutic target to manage the deteriorated metastasis of BrCa and identified DAAM1 as a promising biomarker for unfavorable prognosis in BrCa patients.

Identifiants

pubmed: 31757662
pii: S0344-0338(19)31949-1
doi: 10.1016/j.prp.2019.152736
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
DAAM1 protein, human 0
Microfilament Proteins 0
rho GTP-Binding Proteins EC 3.6.5.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

152736

Informations de copyright

Copyright © 2019 Elsevier GmbH. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no competing interests.

Auteurs

Jie Mei (J)

Department of Physiology, Nanjing Medical University, Nanjing 211166, China; Department of Oncology, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi 214023, China. Electronic address: meijie199621@163.com.

Bujie Xu (B)

Department of Physiology, Nanjing Medical University, Nanjing 211166, China. Electronic address: bujiexu192@163.com.

Leiyu Hao (L)

Department of Physiology, Nanjing Medical University, Nanjing 211166, China. Electronic address: leiyuhao316@163.com.

Zhuang Xiao (Z)

Department of Physiology, Nanjing Medical University, Nanjing 211166, China. Electronic address: xiaozhuang_325@163.com.

Yan Liu (Y)

Department of Physiology, Nanjing Medical University, Nanjing 211166, China. Electronic address: kldliuyan@163.com.

Ting Yan (T)

Safety Assessment and Research Center for Drug, Pesticide and Veterinary Drug of Jiangsu Province, Nanjing Medical University, Nanjing 211166, China. Electronic address: yanting@njmu.edu.cn.

Yichao Zhu (Y)

Department of Physiology, Nanjing Medical University, Nanjing 211166, China; State Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing 211166, China. Electronic address: zhuyichao@njmu.edu.cn.

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Classifications MeSH