Transcribed Ultraconserved Regions Are Associated with Clinicopathological Features in Breast Cancer

被引:3
作者
Zambalde, Erika Pereira [1 ]
Adamoski, Douglas [2 ]
Gradia, Daniela Fiori [1 ]
Rabinovich, Iris [3 ]
Rodrigues, Ana Carolina [1 ]
Ivan, Cristina [4 ]
Ribeiro, Enilze M. S. F. [1 ]
Calin, George Adrian [4 ,5 ]
Carvalho de Oliveira, Jaqueline [1 ]
机构
[1] Univ Fed Parana, Dept Genet, Lab Human Cytogenet & Oncogenet, BR-81531980 Curitiba, PR, Brazil
[2] Brazilian Ctr Res Energy & Mat CNPEM, Brazilian Biosci Natl Lab LNBio, BR-13083970 Campinas, SP, Brazil
[3] Hosp Nossa Senhora Gracas, Ctr Doencas Mama, BR-80810040 Curitiba, PR, Brazil
[4] Univ Texas MD Anderson Canc Ctr, Translat Mol Pathol Dept, Houston, TX 77230 USA
[5] Univ Texas MD Anderson Canc Ctr, Ctr RNA Interference & Noncoding RNAs, Houston, TX 77230 USA
关键词
T-UCRs; breast cancer (BC); lncRNAs; INTERNATIONAL EXPERT CONSENSUS; LONG NONCODING RNA; MOLECULAR PORTRAITS; PRIMARY THERAPY; EXPRESSION;
D O I
10.3390/biom12020214
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
Ultraconserved regions (UCRs) are 481 genome segments, with length longer than 200 bp, that are 100% conserved among humans, mice, and rats. The majority of UCRs are transcriptionally active (T-UCRs) as many of them produce non-coding RNAs. In a previous study, we evaluated the expression level of T-UCRs in breast cancer (BC) patients and found that 63% of transcripts correlated with some clinical and/or molecular parameter of BC. In this study, we delved into the expression levels of 12 T-UCRs and correlated them with clinicopathological parameters, immunohistochemical markers, and overall survival in two breast cancer cohorts: TCGA and Brazilian patients. We found that uc.268 is more expressed in TCGA patients under 40 years of age, associated with progesterone receptor (PR) and estrogen receptor (ER), and its high expression is found in luminal A. Lower uc.84 and uc.376 were respectively observed in metastatic and stage IV tumors associated with good prognostic in luminal B. Moreover, uc.84 was only related to the HER2+, while uc.376 was related to ER+ and PR+, and HER2+. A panel composed of uc.147, uc.271, and uc.427 distinguished luminal A from triple negative patients with an AUC of 0.9531 (sensitivity 92.19% and specificity 86.76%). These results highlight the potential role of T-UCRs in BC and provide insights into the potential application of T-UCRs as biomarkers.
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页数:16
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共 37 条
[1]   Use of Biomarkers to Guide Decisions on Adjuvant Systemic Therapy for Women With Early-Stage Invasive Breast Cancer: ASCO Clinical Practice Guideline Update Summary [J].
Andre, Fabrice ;
Ismaila, Nofisat ;
Stearns, Vered .
JOURNAL OF ONCOLOGY PRACTICE, 2019, 15 (09) :495-+
[2]   Ultraconserved elements in the human genome [J].
Bejerano, G ;
Pheasant, M ;
Makunin, I ;
Stephen, S ;
Kent, WJ ;
Mattick, JS ;
Haussler, D .
SCIENCE, 2004, 304 (5675) :1321-1325
[3]  
Beniey Michele, 2019, Oncoscience, V6, P287, DOI 10.18632/oncoscience.474
[4]   Expression and functional role of a transcribed noncoding RNA with an ultraconserved element in hepatocellular carcinoma [J].
Braconi, Chiara ;
Valeri, Nicola ;
Kogure, Takayuki ;
Gasparini, Pierluigi ;
Huang, Nianyuan ;
Nuovo, Gerard J. ;
Terracciano, Luigi ;
Croce, Carlo M. ;
Patel, Tushar .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (02) :786-791
[5]   The Function of Non-Coding RNAs in Lung Cancer Tumorigenesis [J].
Braicu, Cornelia ;
Zimta, Alina-Andreea ;
Harangus, Antonia ;
Iurca, Ioana ;
Irimie, Alexandru ;
Coza, Ovidiu ;
Berindan-Neagoe, Ioana .
CANCERS, 2019, 11 (05)
[6]   The long and the short of noncoding RNAs [J].
Brosnan, Christopher A. ;
Voinnet, Olivier .
CURRENT OPINION IN CELL BIOLOGY, 2009, 21 (03) :416-425
[7]   Expression of a family of noncoding mitochondrial RNAs distinguishes normal from cancer cells [J].
Burzio, Veronica A. ;
Villota, Claudio ;
Villegas, Jaime ;
Landerer, Eduardo ;
Boccardo, Enrique ;
Villa, Luisa L. ;
Martinez, Ronny ;
Lopez, Constanza ;
Gaete, Fancy ;
Toro, Viviana ;
Rodriguez, Ximena ;
Burzio, Luis O. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (23) :9430-9434
[8]   Ultraconserved regions encoding ncRNAs are, altered in human leukemias and carcinomas [J].
Calin, George A. ;
Liu, Chang-Gong ;
Ferracin, Manuela ;
Hyslop, Terry ;
Spizzo, Riccardo ;
Sevignani, Cinzia ;
Fabbri, Muller ;
Cimmino, Amelia ;
Lee, Eun Joo ;
Wojcik, Sylwia E. ;
Shimizu, Masayoshi ;
Tili, Esmerina ;
Rossi, Simona ;
Taccioli, Cristian ;
Pichiorri, Flavia ;
Liu, Xiuping ;
Zupo, Simona ;
Herlea, Vlad ;
Gramantieri, Laura ;
Lanza, Giovanni ;
Alder, Hansjuerg ;
Rassenti, Laura ;
Volinia, Stefano ;
Schmittgen, Thomas D. ;
Kipps, Thomas J. ;
Negrini, Massimo ;
Croce, Carlo M. .
CANCER CELL, 2007, 12 (03) :215-229
[9]   Wnt signalling modulates transcribed-ultraconserved regions in hepatobiliary cancers [J].
Carotenuto, Pietro ;
Fassan, Matteo ;
Pandolfo, Rosantony ;
Lampis, Andrea ;
Vicentini, Caterina ;
Cascione, Luciano ;
Paulus-Hock, Viola ;
Boulter, Luke ;
Guest, Rachel ;
Quagliata, Luca ;
Hahne, Jens Claus ;
Ridgway, Rachel ;
Jamieson, Tam ;
Athineos, Dimitris ;
Veronese, Angelo ;
Visone, Rosa ;
Murgia, Claudio ;
Ferrari, Giulia ;
Guzzardo, Vincenza ;
Evans, Thomas Ronald Jeffry ;
MacLeod, Martin ;
Feng, Gui Ji ;
Dale, Trevor ;
Negrini, Massimo ;
Forbes, Stuart J. ;
Terracciano, Luigi ;
Scarpa, Aldo ;
Patel, Tushar ;
Valeri, Nicola ;
Workman, Paul ;
Sansom, Owen ;
Braconi, Chiara .
GUT, 2017, 66 (07) :1268-1277
[10]   Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer [J].
Ciriello, Giovanni ;
Gatza, Michael L. ;
Beck, Andrew H. ;
Wilkerson, Matthew D. ;
Rhie, Suhn K. ;
Pastore, Alessandro ;
Zhang, Hailei ;
McLellan, Michael ;
Yau, Christina ;
Kandoth, Cyriac ;
Bowlby, Reanne ;
Shen, Hui ;
Hayat, Sikander ;
Fieldhouse, Robert ;
Lester, Susan C. ;
Tse, Gary M. K. ;
Factor, Rachel E. ;
Collins, Laura C. ;
Allison, Kimberly H. ;
Chen, Yunn-Yi ;
Jensen, Kristin ;
Johnson, Nicole B. ;
Oesterreich, Steffi ;
Mills, Gordon B. ;
Cherniack, Andrew D. ;
Robertson, Gordon ;
Benz, Christopher ;
Sander, Chris ;
Laird, Peter W. ;
Hoadley, Katherine A. ;
King, Tari A. ;
Perou, Charles M. .
CELL, 2015, 163 (02) :506-519