HOXA5 determines cell fate transition and impedes tumor initiation and progression in breast cancer through regulation of E-cadherin and CD24.

Teo, W W; Merino, V F; Cho, S; Korangath, P; Liang, X; Wu, R-C; Neumann, N M; Ewald, A J; Sukumar, S

Teo, W W; Merino, V F; Cho, S; Korangath, P; Liang, X; Wu, R-C; Neumann, N M; Ewald, A J; Sukumar, S.

Affiliation

Teo WW; Department of Oncology, Johns Hopkins University School of Medicine, Breast Cancer Program Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD, USA.
Merino VF; Graduate Program in Pathobiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Cho S; Department of Oncology, Johns Hopkins University School of Medicine, Breast Cancer Program Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD, USA.
Korangath P; Department of Oncology, Johns Hopkins University School of Medicine, Breast Cancer Program Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD, USA.
Liang X; Department of Oncology, Johns Hopkins University School of Medicine, Breast Cancer Program Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD, USA.
Wu RC; Department of Oncology, Johns Hopkins University School of Medicine, Breast Cancer Program Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD, USA.
Neumann NM; Graduate Program in Pathobiology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Ewald AJ; Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sukumar S; Department of Cell Biology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Oncogene ; 35(42): 5539-5551, 2016 10 20.

Article de En | MEDLINE | ID: mdl-27157614

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Tumeurs du sein / Cadhérines / Régulation de l'expression des gènes tumoraux / Transformation cellulaire néoplasique / Protéines à homéodomaine / Antigènes CD24 Type d'étude: Prognostic_studies Limites: Animals / Female / Humans Langue: En Journal: Oncogene Sujet du journal: BIOLOGIA MOLECULAR / NEOPLASIAS Année: 2016 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Royaume-Uni

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