LncRNA loc285194 is a p53-regulated tumor suppressor

被引:345
|
作者
Liu, Qian [1 ,2 ]
Huang, Jianguo [1 ,3 ]
Zhou, Nanjiang [1 ,3 ]
Zhang, Ziqiang [3 ]
Zhang, Ali [1 ]
Lu, Zhaohui [4 ]
Wu, Fangting [5 ]
Mo, Yin-Yuan [1 ,3 ]
机构
[1] So Illinois Univ, Sch Med, Dept Med Microbiol Immunol & Cell Biol, Springfield, IL USA
[2] Chongqing Med Univ, Inst Neurosci, Chongqing 400016, Peoples R China
[3] Univ Mississippi, Med Ctr, Inst Canc, Jackson, MS 39216 USA
[4] Peoples Liberat Army Gen Hosp, Dept Endocrinol, Beijing 100853, Peoples R China
[5] Syst Biosci, Mountain View, CA USA
基金
美国国家卫生研究院;
关键词
LONG NONCODING RNA; HOST GENE; MICRORNA; CHROMATIN; ACTIVATION; CANCER; TRANSCRIPTION; EXPRESSION; PTEN; HULC;
D O I
10.1093/nar/gkt182
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein-coding genes account for only a small part of the human genome, whereas the vast majority of transcripts make up the non-coding RNAs including long non-coding RNAs (lncRNAs). Accumulating evidence indicates that lncRNAs could play a critical role in regulation of cellular processes such as cell growth and apoptosis as well as cancer progression and metastasis. LncRNA loc285194 was previously shown to be within a tumor suppressor unit in osteosarcoma and to suppress tumor cell growth. However, it is unknown regarding the regulation of loc285194. Moreover, the underlying mechanism by which loc285194 functions as a potential tumor suppressor is elusive. In this study, we show that loc285194 is a p53 transcription target; ectopic expression of loc285194 inhibits tumor cell growth both in vitro and in vivo. Through deletion analysis, we identify an active region responsible for tumor cell growth inhibition within exon 4, which harbors two miR-211 binding sites. Importantly, this loc285194-mediated growth inhibition is in part due to specific suppression of miR-211. We further demonstrate a reciprocal repression between loc285194 and miR-211; in contrast to loc285194, miR-211 promotes cell growth. Finally, we detect downregulation of loc285194 in colon cancer specimens by quantitative PCR arrays and in situ hybridization of tissue microarrays. Together, these results suggest that loc285194 is a p53-regulated tumor suppressor, which acts in part through repression of miR-211.
引用
收藏
页码:4976 / 4987
页数:12
相关论文
共 50 条
  • [31] DNA repair inhibitor effect on p53-regulated apoptosis
    Geske, FJ
    Lieberman, R
    Strange, R
    Gerschenson, LE
    FASEB JOURNAL, 2000, 14 (04): : A196 - A196
  • [32] Constitutive DNase I hypersensitivity of p53-regulated promoters
    Braastad, CD
    Han, ZY
    Hendrickson, EA
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (10) : 8261 - 8268
  • [33] lncRNA LOC285194在肾癌组织中的表达及其对786-O细胞增殖、迁移与侵袭的影响
    刘明兴
    王科峰
    裴冬梅
    解剖科学进展, 2020, 26 (04) : 413 - 416
  • [34] ONCOGENIC FORMS OF P53 INHIBIT P53-REGULATED GENE-EXPRESSION
    KERN, SE
    PIETENPOL, JA
    THIAGALINGAM, S
    SEYMOUR, A
    KINZLER, KW
    VOGELSTEIN, B
    SCIENCE, 1992, 256 (5058) : 827 - 830
  • [35] p53-regulated lncRNAs in cancers: from proliferation and metastasis to therapy
    Yang, Kaixin
    Xiao, Yinan
    Zhong, Linghui
    Zhang, Wenyang
    Wang, Peng
    Ren, Yaru
    Shi, Lei
    CANCER GENE THERAPY, 2023, 30 (11) : 1456 - 1470
  • [36] Inhibition of p53-induced apoptosis without affecting expression of p53-regulated genes
    Lotem, J
    Gal, H
    Kama, R
    Amariglio, N
    Rechavi, G
    Domany, E
    Sachs, L
    Givol, D
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) : 6718 - 6723
  • [37] p53-regulated lncRNAs in cancers: from proliferation and metastasis to therapy
    Kaixin Yang
    Yinan Xiao
    Linghui Zhong
    Wenyang Zhang
    Peng Wang
    Yaru Ren
    Lei Shi
    Cancer Gene Therapy, 2023, 30 : 1456 - 1470
  • [38] Hyperglycemia activates p53 and p53-regulated genes leading to myocyte cell death
    Fiordaliso, F
    Leri, A
    Cesselli, D
    Limana, F
    Safai, B
    Nadal-Ginard, B
    Anversa, P
    Kajstura, J
    DIABETES, 2001, 50 (10) : 2363 - 2375
  • [39] p53-regulated autophagy is controlled by glycolysis and determines cell fate
    Duan, Lei
    Perez, Ricardo E.
    Davaadelger, Batzaya
    Dedkova, Elena N.
    Blatter, Lothar A.
    Maki, Carl G.
    ONCOTARGET, 2015, 6 (27) : 23135 - 23156
  • [40] CHARACTERIZATION OF HUMAN GADD45, A P53-REGULATED PROTEIN
    CARRIER, F
    SMITH, ML
    BAE, I
    KILPATRICK, KE
    LANSING, TJ
    CHEN, CY
    ENGELSTEIN, M
    FRIEND, SH
    HENNER, WD
    GILMER, TM
    KASTAN, MB
    FORNACE, AJ
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1994, 269 (51) : 32672 - 32677