A p53/lnc‐Ip53 Negative Feedback Loop Regulates Tumor Growth and Chemoresistance

• Published in: Advanced science Vol. 7; no. 21; pp. 2001364 - n/a
• Main Authors: Zhang, Li‐Zhen, Yang, Jin‐E, Luo, Yu‐Wei, Liu, Feng‐Ting, Yuan, Yun‐Fei, Zhuang, Shi‐Mei
• Format: Journal Article
• Language: English
• Published: Weinheim John Wiley & Sons, Inc 01.11.2020; John Wiley and Sons Inc; Wiley
• Subjects: acetylation; Antibodies; Apoptosis; Binding sites; Cell cycle; Deoxyribonucleic acid; DNA; DNA damage; Kinases; lnc‐Ip53; non‐coding RNA; p53; Physiology; Proteins; tumor growth
• ISSN: 2198-3844; 2198-3844
• DOI: 10.1002/advs.202001364

Acetylation is a critical mechanism to modulate tumor‐suppressive activity of p53, but the causative roles of long non‐coding RNAs (lncRNAs) in p53 acetylation and their biological significance remain unexplored. Here, lncRNA LOC100294145 is discovered to be transactivated by p53 and is thus designated as lnc‐Ip53 for lncRNA induced by p53. Furthermore, lnc‐Ip53 impedes p53 acetylation by interacting with histone deacetylase 1 (HDAC1) and E1A binding protein p300 (p300) to prevent HDAC1 degradation and attenuate p300 activity, resulting in abrogation of p53 activity and subsequent cell proliferation and apoptosis resistance. Mouse xenograft models reveal that lnc‐Ip53 promotes tumor growth and chemoresistance in vivo, which is attenuated by an HDAC inhibitor. Silencing lnc‐Ip53 inhibits the growth of xenografts with wild‐type p53, but not those expressing acetylation‐resistant p53. Consistently, lnc‐Ip53 is upregulated in multiple cancer types, including hepatocellular carcinoma (HCC). High levels of lnc‐Ip53 is associated with low levels of acetylated p53 in human HCC and mouse xenografts, and is also correlated with poor survival of HCC patients. These findings identify a novel p53/lnc‐Ip53 negative feedback loop in cells and indicate that abnormal upregulation of lnc‐Ip53 represents an important mechanism to inhibit p53 acetylation/activity and thereby promote tumor growth and chemoresistance, which may be exploited for anticancer therapy. Acetylation is indispensable for activation of tumor suppressor p53. LncRNA lnc‐Ip53 is induced by p53 and in turn represses p53 acetylation by interacting with HDAC1 and p300 to prevent HDAC1 degradation and attenuate p300 activity, which consequently abrogates p53 activity and thus facilitates cell proliferation and apoptosis resistance. Abnormal upregulation of lnc‐Ip53 in tumors promotes tumor growth and confers chemoresistance.