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PMID: 29378908 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The Transcription Factor AP4 Promotes Oncogenic Phenotypes and Cisplatin Resistance by Regulating LAPTM4B Expression.

Molecular cancer research : MCR ·Vol. 16 ·No. 5 ·2018-00-00 ·Pages 857-868

Wang L, Meng Y, Xu JJ, Zhang QY

Abstract

Lysosomal-associated protein transmembrane-4 beta (LAPTM4B) is a novel oncogene, whose overexpression is involved in cancer occurrence and progression. However, the mechanism of LAPTM4B transcriptional regulation remains unclear. In this study, the results of transcription factor (TF) profiling plate arrays indicated that AP4 was a potential transcription factor regulating LAPTM4B expression. LAPTM4B was positively correlated with AP4 and they were both associated with poor overall and disease-free survival. Luciferase and electrophoretic mobility shift assay assays confirmed that AP4 directly bound to the polymorphism region of LAPTM4B promoter and modulated its transcription. Functionally, AP4 promoted cell proliferation, migration, invasion, and assisted drug resistance in part through upregulation of LAPTM4B. Taken together, these findings identify LAPTM4B as a direct AP4 target gene and the interaction of AP4 and LAPTM4B plays an important role in breast cancer progression.Implications: This study demonstrates that AP4 promotes cell growth, migration, invasion, and cisplatin resistance through upregulation of LAPTM4B expression, thus representing an attractive therapeutic target for breast cancer. Mol Cancer Res; 16(5); 857-68. ©2018 AACR.

MeSH Terms
Animals Antineoplastic Agents/pharmacology Basic Helix-Loop-Helix Leucine Zipper Transcription Factors/genetics,metabolism Breast Neoplasms/genetics,metabolism,pathology Carcinogenesis Cell Line, Tumor Cell Movement/physiology Cell Proliferation/physiology Cisplatin/pharmacology DNA-Binding Proteins Drug Resistance, Neoplasm Female Heterografts Humans MCF-7 Cells Membrane Proteins/biosynthesis,genetics,metabolism Mice Mice, Inbred NOD Mice, SCID Oncogene Proteins/biosynthesis,genetics,metabolism Phenotype RNA-Binding Proteins Transfection
Chemicals
Antineoplastic Agents Basic Helix-Loop-Helix Leucine Zipper Transcription Factors DNA-Binding Proteins LAPTM4B protein, human Membrane Proteins Oncogene Proteins REPIN1 protein, human RNA-Binding Proteins Cisplatin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wang Lu
Department of Clinical Laboratory, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University School of Oncology, Beijing Cancer Hospital & Institute, Beijing, China.
Meng Yue
Department of Clinical Laboratory, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University School of Oncology, Beijing Cancer Hospital & Institute, Beijing, China.
Xu Jian-Jun
Department of Clinical Laboratory, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University School of Oncology, Beijing Cancer Hospital & Institute, Beijing, China.
Zhang Qing-Yun
Department of Clinical Laboratory, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University School of Oncology, Beijing Cancer Hospital & Institute, Beijing, China. zhqy_208@163.com.
Article Info
Journal
Molecular cancer research : MCR
Abbr.
Mol Cancer Res
ISSN
1557-3125
Published
2018-00-00
Epub
2018-00-29
Pages
857-868
Language
English
Region
United States
NLM ID
101150042
Subset
IM
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