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cAMP Responsive Element Binding Protein-1 Is a Transcription Factor of Lysosomal-Associated Protein Transmembrane-4 beta in Human Breast Cancer Cells
被引:18
|作者:
Zhang, Meng
[1
]
Xu, Jian-Jun
[1
]
Zhou, Rou-Li
[2
]
Zhang, Qing-Yun
[1
]
机构:
[1] Peking Univ, Canc Hosp & Inst, Key Lab Carcinogenesis & Translat Res, Minist Educ,Dept Clin Lab, Beijing 100871, Peoples R China
[2] Peking Univ, Sch Basic Med Sci, Dept Cell Biol, Beijing 100871, Peoples R China
来源:
PLOS ONE
|
2013年
/
8卷
/
02期
基金:
中国国家自然科学基金;
关键词:
HEPATOCELLULAR-CARCINOMA;
GALLBLADDER CARCINOMA;
DOWN-REGULATION;
CREB;
LAPTM4B-35;
EXPRESSION;
OVEREXPRESSION;
GENE;
PHOSPHORYLATION;
RESISTANCE;
D O I:
10.1371/journal.pone.0057520
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Lysosomal-associated protein transmembrane-4 beta (LAPTM4B) is a potential proto-oncogene, whose overexpression is involved in cancer occurrence and progression. Its transcript is up-regulated in various types of solid tumors including breast cancer. However, its transcriptional regulation mechanism is still unclear. To investigate the mechanism of transcriptional regulation of LAPTM4B in human breast cancer cells, a series of luciferase reporter constructs and construct with mutated binding site for cAMP responsive element binding protein-1 (CREB1) were generated by PCR amplification and transiently transfected into breast cancer cells to determine the transcriptional activities of different promoter regions. The + 10 similar to+ 292 promoter region was possessed the highest transcriptional activity. The ability of CREB1 to bind the LAPMT4B promoter was confirmed by electrophoretic mobility shift assay, super-shift and RNA interference experiments. Our study identified the core promoter region responsible for constitutive expression of LAPTM4B and clarified that CREB1 played an important role in LAPTM4B transcriptional regulation in human breast cancer cells.
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页数:7
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