ING5 suppresses breast cancer progression and is regulated by miR-24

Author:

Cui Shufang,Liao Xin,Ye Chao,Yin Xin,Liu Minghui,Hong Yeting,Yu Mengchao,Liu Yanqing,Liang Hongwei,Zhang Chen-Yu,Chen Xi

Funder

National Basic Research Program of China

National Natural Science Foundation of China

Research Special Fund for Public Welfare Industry of Health

Natural Science Foundation of Jiangsu Province

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology,Molecular Medicine

Reference29 articles.

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2. Gunduz M, Gunduz E, Rivera RS, Nagatsuka H. The inhibitor of growth (ING) gene family: potential role in cancer therapy. Curr Cancer Drug Targets. 2008;8:275–84.

3. Soliman MA, Riabowol K. After a decade of study-ING, a PHD for a versatile family of proteins. Trends Biochem Sci. 2007;32:509–19.

4. Gou WF, Shen DF, Yang XF, Zhao S, Liu YP, Sun HZ, Su RJ, Luo JS, Zheng HC. ING5 suppresses proliferation, apoptosis, migration and invasion, and induces autophagy and differentiation of gastric cancer cells: a good marker for carcinogenesis and subsequent progression. Oncotarget. 2015;6:19552–79.

5. Shiseki M, Nagashima M, Pedeux RM, Kitahama-Shiseki M, Miura K, Okamura S, Onogi H, Higashimoto Y, Appella E, Yokota J, Harris CC. p29ING4 and p28ING5 bind to p53 and p300, and enhance p53 activity. Cancer Res. 2003;63:2373–8.

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