Long Noncoding RNAs in Cancer and Therapeutic Potential

被引:229
作者
Renganathan, Arun [1 ]
Felley-Bosco, Emanuela [2 ]
机构
[1] Jawaharlal Nehru Ctr Adv Sci Res, Mol Biol & Genet Unit, Bangalore, Karnataka, India
[2] Univ Hosp Zurich, Mol Oncol Lab, Div Thorac Surg, Zurich, Switzerland
来源
LONG NON CODING RNA BIOLOGY | 2017年 / 1008卷
关键词
Cancer; Natural antisense transcripts; Antisense oligonucleotides; Chemoresistance; Epigenetic regulation; Therapeutic target; Gene regulation; ceRNA; NATURAL ANTISENSE TRANSCRIPTS; PROSTATE-CANCER; TUMOR-SUPPRESSOR; MESSENGER-RNA; CELL-PROLIFERATION; C-MYC; HEPATOCELLULAR-CARCINOMA; COLORECTAL-CANCER; DRUG-RESISTANCE; GENE-EXPRESSION;
D O I
10.1007/978-981-10-5203-3_7
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Long noncoding RNAs (lncRNAs) are the major elements of the mammalian transcriptome that is emerging as a central player controlling diverse cellular mechanisms. Most of the well-studied lncRNAs so far are found to be crucial in regulating cellular processes such as cell cycle, growth, and apoptosis that ensure homeostasis. Owing to their location and distribution in the genome, lncRNAs influence the transcription of a wide range of proteins directly or indirectly by transcriptional and posttranscriptional alterations, which opens up the "LncRNA-cancer paradigm" in a context-dependent manner, i.e., either oncogenic or tumor suppressive. Thus, this chapter is a consolidation of lncRNA association in exhibiting or suppressing the typical cancer hallmarks such as continuous proliferation, surpassing apoptosis, genomic instability, drug resistance, invasion, and metastasis studied till date. In addition, special focus has been given on the efficient application of lncRNAs as potential targets for therapeutics that holds a great promise for future cancer therapy.
引用
收藏
页码:199 / 222
页数:24
相关论文
共 130 条
[1]   p53 induces formation of NEAT1 lncRNA-containing paraspeckles that modulate replication stress response and chemosensitivity [J].
Adriaens, Carmen ;
Standaert, Laura ;
Barra, Jasmine ;
latil, MathilDe ;
Verfaillie, Annelien ;
Kalev, Peter ;
Boeckx, Bram ;
Wijnhoven, Paul W. G. ;
Radaelli, Enrico ;
Vermi, William ;
Leucci, Eleonora ;
Lapouge, Gaelle ;
Beck, Benjamin ;
van den Oord, Joost ;
Nakagawa, Shinichi ;
Hirose, Tetsuro ;
Sablina, Anna A. ;
Lambrechts, Diether ;
Aerts, Stein ;
Blanpain, Cedric ;
Marine, Jean-Christophe .
NATURE MEDICINE, 2016, 22 (08) :861-+
[2]   Differentiation of mammary tumors and reduction in metastasis upon Malat1 lncRNA loss [J].
Arun, Gayatri ;
Diermeier, Sarah ;
Akerman, Martin ;
Chang, Kung-Chi ;
Wilkinson, J. Erby ;
Hearn, Stephen ;
Kim, Youngsoo ;
MacLeod, A. Robert ;
Krainer, Adrian R. ;
Norton, Larry ;
Brogi, Edi ;
Egeblad, Mikala ;
Spector, David L. .
GENES & DEVELOPMENT, 2016, 30 (01) :34-51
[3]   The c-Myc oncogene directly induces the H19 noncoding RNA by allele-specific binding to potentiate tumorigenesis [J].
Barsyte-Lovejoy, Dalia ;
Lau, Suzanne K. ;
Boutros, Paul C. ;
Khosravi, Fereshteh ;
Jurisica, Igor ;
Andrulis, Irene L. ;
Tsao, Ming S. ;
Penn, Linda Z. .
CANCER RESEARCH, 2006, 66 (10) :5330-5337
[4]   Long noncoding RNAs in cancer: mechanisms of action and technological advancements [J].
Bartonicek, Nenad ;
Maag, Jesper L. V. ;
Dinger, Marcel E. .
MOLECULAR CANCER, 2016, 15
[5]   The Snail repressor recruits EZH2 to specific genomic sites through the enrollment of the lncRNA HOTAIR in epithelial-to-mesenchymal transition [J].
Battistelli, C. ;
Cicchini, C. ;
Santangelo, L. ;
Tramontano, A. ;
Grassi, L. ;
Gonzalez, F. J. ;
de Nonno, V. ;
Grassi, G. ;
Amicone, L. ;
Tripodi, M. .
ONCOGENE, 2017, 36 (07) :942-955
[6]   A natural antisense transcript regulates Zeb2/Sip1 gene expression during Snail1-induced epithelial-mesenchymal transition [J].
Beltran, Manuel ;
Puig, Isabel ;
Pena, Cristina ;
Miguel Garcia, Jose ;
Belen Alvarez, Ana ;
Pena, Raul ;
Bonilla, Felix ;
Garcia de Herreros, Antonio .
GENES & DEVELOPMENT, 2008, 22 (06) :756-769
[7]   LncRNA-UCA1 enhances cell proliferation and 5-fluorouracil resistance in colorectal cancer by inhibiting miR-204-5p [J].
Bian, Zehua ;
Jin, Liugen ;
Zhang, Jiwei ;
Yin, Yuan ;
Quan, Chao ;
Hu, Yaling ;
Feng, Yuyang ;
Liu, Heyong ;
Fei, Bojian ;
Mao, Yong ;
Zhou, Leyuan ;
Qi, Xiaowei ;
Huang, Shenlin ;
Hua, Dong ;
Xing, Chungen ;
Huang, Zhaohui .
SCIENTIFIC REPORTS, 2016, 6
[8]   Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project [J].
Birney, Ewan ;
Stamatoyannopoulos, John A. ;
Dutta, Anindya ;
Guigo, Roderic ;
Gingeras, Thomas R. ;
Margulies, Elliott H. ;
Weng, Zhiping ;
Snyder, Michael ;
Dermitzakis, Emmanouil T. ;
Stamatoyannopoulos, John A. ;
Thurman, Robert E. ;
Kuehn, Michael S. ;
Taylor, Christopher M. ;
Neph, Shane ;
Koch, Christoph M. ;
Asthana, Saurabh ;
Malhotra, Ankit ;
Adzhubei, Ivan ;
Greenbaum, Jason A. ;
Andrews, Robert M. ;
Flicek, Paul ;
Boyle, Patrick J. ;
Cao, Hua ;
Carter, Nigel P. ;
Clelland, Gayle K. ;
Davis, Sean ;
Day, Nathan ;
Dhami, Pawandeep ;
Dillon, Shane C. ;
Dorschner, Michael O. ;
Fiegler, Heike ;
Giresi, Paul G. ;
Goldy, Jeff ;
Hawrylycz, Michael ;
Haydock, Andrew ;
Humbert, Richard ;
James, Keith D. ;
Johnson, Brett E. ;
Johnson, Ericka M. ;
Frum, Tristan T. ;
Rosenzweig, Elizabeth R. ;
Karnani, Neerja ;
Lee, Kirsten ;
Lefebvre, Gregory C. ;
Navas, Patrick A. ;
Neri, Fidencio ;
Parker, Stephen C. J. ;
Sabo, Peter J. ;
Sandstrom, Richard ;
Shafer, Anthony .
NATURE, 2007, 447 (7146) :799-816
[9]   Noncoding RNA transcription beyond annotated genes [J].
Carninci, Piero ;
Hayashizaki, Yoshihide .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2007, 17 (02) :139-144
[10]   aHIF but not HIF-1α transcript is a poor prognostic marker in human breast cancer [J].
Cayre, A ;
Rossignol, F ;
Clottes, E ;
Penault-Llorca, F .
BREAST CANCER RESEARCH, 2003, 5 (06) :R223-R230