Nuclear-enriched abundant transcript 1 as a diagnostic and prognostic biomarker in colorectal cancer

被引:138
作者
Wu, Yuchen [1 ,2 ]
Yang, Li [1 ,2 ]
Zhao, Jiang [1 ,2 ]
Li, Cong [1 ,2 ]
Nie, Jia [3 ]
Liu, Fangqi [1 ,2 ]
Zhuo, Changhua [4 ]
Zheng, Yaxin [5 ]
Li, Bin [3 ]
Wang, Zhimin [6 ,7 ]
Xu, Ye [1 ,2 ]
机构
[1] Fudan Univ, Shanghai Canc Ctr, Dept Colorectal Surg, Shanghai 20032, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai 20032, Peoples R China
[3] Chinese Acad Sci, Inst Pasteur Shanghai, Shanghai Inst Biol Sci, Unit Mol Immunol,Key Lab Mol Virol & Immunol, Shanghai 20031, Peoples R China
[4] Fujian Med Univ, Teaching Hosp, Dept Surg Oncol, Fujian Prov Canc Hosp, Fuzhou 350014, Peoples R China
[5] Second Mil Med Univ, Eastern Hepatobiliary Hosp, Shanghai 200438, Peoples R China
[6] Chinese Natl Human Genome Ctr, Shanghai MOST Key Lab Hlth & Dis Genom, Dept Genet, Shanghai 201203, Peoples R China
[7] Shanghai Ind Technol Inst, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomarker; Prognosis; Diagnosis; Colorectal cancer; Long non-coding RNA; LONG NONCODING RNA; LYMPHOCYTE RATIO; LNCRNA NEAT1; NEUTROPHIL; EXPRESSION; IDENTIFICATION; VALIDATION; SURVIVAL;
D O I
10.1186/s12943-015-0455-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Background: High expression of the long non-coding RNA nuclear-enriched abundant transcript 1 (NEAT1) in whole blood has been reported in colorectal cancer patients; however, its' clinical significance and origin are unclear. We evaluated the diagnostic and prognostic value, and origin of whole blood NEAT1 in colorectal cancer. Methods: Expression of NEAT1 variants, NEAT1_v1 and NEAT1_v2 were determined using real-time quantitative PCR. The diagnostic value of whole blood NEAT1 expression was evaluated in test (n = 60) and validation (n = 200) cohorts of colorectal cancer patients and normal controls (NCs). To identify the origin of NEAT1, its expression was analyzed in blood, matched primary tumor tissues, para-tumor tissues, metastatic tissues, and also immune cells from patients or NCs. Function of NEAT1 in colorectal cell lines was also assessed. The correlation of NEAT1 expression with clinical outcomes was assessed in 191 patients. Results: Whole blood NEAT1 expression was significantly higher in colorectal cancer patients than in NCs. NEAT1_v1 and NEAT1_v2 expression were highly accurate in distinguishing colorectal cancer patients from NCs (area under the curve: 0.787 and 0.871, respectively). Knockdown of NEAT1_v1 in vitro could inhibit cell invasion and proliferation, while knockdown of NEAT1_v2 promoted cell growth. However, whole blood expression was not correlated with matched tissues. An elevated expression was seen in neutrophils from CRC patients. Furthermore, high expression of NEAT1_v1 was correlated with worse overall survival. In contrast, high expression of NEAT1_v2 alone was correlated with better overall survival. Conclusion: Whole blood NEAT1 expression is a novel diagnostic and prognostic biomarker of overall survival in colorectal cancer. Elevated NEAT1 may derive from neutrophils.
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页数:12
相关论文
共 50 条
[1]
MicroRNAome Genome: A Treasure for Cancer Diagnosis and Therapy [J].
Berindan-Neagoe, Ioana ;
Monroig, Paloma del C. ;
Pasculli, Barbara ;
Calin, George A. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2014, 64 (05) :311-336
[2]
The transcriptional landscape of the mammalian genome [J].
Carninci, P ;
Kasukawa, T ;
Katayama, S ;
Gough, J ;
Frith, MC ;
Maeda, N ;
Oyama, R ;
Ravasi, T ;
Lenhard, B ;
Wells, C ;
Kodzius, R ;
Shimokawa, K ;
Bajic, VB ;
Brenner, SE ;
Batalov, S ;
Forrest, ARR ;
Zavolan, M ;
Davis, MJ ;
Wilming, LG ;
Aidinis, V ;
Allen, JE ;
Ambesi-Impiombato, X ;
Apweiler, R ;
Aturaliya, RN ;
Bailey, TL ;
Bansal, M ;
Baxter, L ;
Beisel, KW ;
Bersano, T ;
Bono, H ;
Chalk, AM ;
Chiu, KP ;
Choudhary, V ;
Christoffels, A ;
Clutterbuck, DR ;
Crowe, ML ;
Dalla, E ;
Dalrymple, BP ;
de Bono, B ;
Della Gatta, G ;
di Bernardo, D ;
Down, T ;
Engstrom, P ;
Fagiolini, M ;
Faulkner, G ;
Fletcher, CF ;
Fukushima, T ;
Furuno, M ;
Futaki, S ;
Gariboldi, M .
SCIENCE, 2005, 309 (5740) :1559-1563
[3]
The oestrogen receptor alpha-regulated lncRNA NEAT1 is a critical modulator of prostate cancer [J].
Chakravarty, Dimple ;
Sboner, Andrea ;
Nair, Sujit S. ;
Giannopoulou, Eugenia ;
Li, Ruohan ;
Hennig, Sven ;
Mosquera, Juan Miguel ;
Pauwels, Jonathan ;
Park, Kyung ;
Kossai, Myriam ;
MacDonald, Theresa Y. ;
Fontugne, Jacqueline ;
Erho, Nicholas ;
Vergara, Ismael A. ;
Ghadessi, Mercedeh ;
Davicioni, Elai ;
Jenkins, Robert B. ;
Palanisamy, Nallasivam ;
Chen, Zhengming ;
Nakagawa, Shinichi ;
Hirose, Tetsuro ;
Bander, Neil H. ;
Beltran, Himisha ;
Fox, Archa H. ;
Elemento, Olivier ;
Rubin, Mark A. .
NATURE COMMUNICATIONS, 2014, 5
[4]
Report of incidence and mortality in China cancer registries, 2009 [J].
Chen, Wanqing ;
Zheng, Rongshou ;
Zhang, Siwei ;
Zhao, Ping ;
Li, Guanglin ;
Wu, Lingyou ;
He, Jie .
CHINESE JOURNAL OF CANCER RESEARCH, 2013, 25 (01) :10-21
[5]
Choudhry H., 2014, Oncogene
[6]
An Architectural Role for a Nuclear Noncoding RNA: NEAT1 RNA Is Essential for the Structure of Paraspeckles [J].
Clemson, Christine M. ;
Hutchinson, John N. ;
Sara, Sergio A. ;
Ensminger, Alexander W. ;
Fox, Archa H. ;
Chess, Andrew ;
Lawrence, Jeanne B. .
MOLECULAR CELL, 2009, 33 (06) :717-726
[7]
CXCR2 and CXCR4 antagonistically regulate neutrophil trafficking from murine bone marrow [J].
Eash, Kyle J. ;
Greenbaum, Adam M. ;
Gopalan, Priya K. ;
Link, Daniel C. .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (07) :2423-2431
[8]
Transcriptomic Analysis Comparing Tumor-Associated Neutrophils with Granulocytic Myeloid-Derived Suppressor Cells and Normal Neutrophils [J].
Fridlender, Zvi G. ;
Sun, Jing ;
Mishalian, Inbal ;
Singhal, Sunil ;
Cheng, Guanjun ;
Kapoor, Veena ;
Horng, Wenhwai ;
Fridlender, Gil ;
Bayuh, Rachel ;
Worthen, G. Scott ;
Albelda, Steven M. .
PLOS ONE, 2012, 7 (02)
[9]
Tumor-associated neutrophils: friend or foe? [J].
Fridlender, Zvi G. ;
Albelda, Steven M. .
CARCINOGENESIS, 2012, 33 (05) :949-955
[10]
Polarization of Tumor-Associated Neutrophil Phenotype by TGF-β: "N1" versus "N2" TAN [J].
Fridlender, Zvi G. ;
Sun, Jing ;
Kim, Samuel ;
Kapoor, Veena ;
Cheng, Guanjun ;
Ling, Leona ;
Worthen, G. Scott ;
Albelda, Steven M. .
CANCER CELL, 2009, 16 (03) :183-194