Analysis of the role of Ly-1 antibody reactive in different cancer types

被引:3
作者
Chen, Linlin [1 ,2 ]
Jin, Congwen [1 ,2 ]
Liu, Hao [1 ,2 ]
Feng, Rongmei [3 ,4 ]
Li, Zhengdong [1 ,2 ]
Zhang, Jiasheng [5 ,6 ]
机构
[1] West Anhui Hlth Vocat Coll, Affiliated Hosp, Gen Surg, Luan, Peoples R China
[2] West Anhui Hlth Vocat Coll, Luan, Peoples R China
[3] Anhui Med Univ, Luan Hosp, Crit Care Med, Luan, Peoples R China
[4] Luan Peoples Hosp, Crit Care Med, Luan, Peoples R China
[5] Anhui Med Univ, Luan Hosp, Emergency Surg, Luan, Peoples R China
[6] Luan Peoples Hosp, Emergency Surg, Luan, Peoples R China
关键词
LYAR; hepatocellular carcinoma; tcga; prognosis; cancer; NUCLEOLAR PROTEIN; LYAR; EXPRESSION;
D O I
10.1080/21655979.2021.1995100
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
LYAR (Ly-1 antibody reactive) is a transcription factor with a specific DNA-binding domain, which plays a key role in the regulation of embryonic stem cell self-renewal and differentiation. However, the role of LYAR in human cancers remains unclear. This study aimed to analyze the prognostic value of LYAR in cancer. In this study, we evaluated the prognostic value of LYAR in various tumors. We research found that, compared with normal tissues, LYAR levels werehigher in a variety of tumors. LYAR expression level was associated with poor overall survival, progression-free interval, and disease-specific survival. LYAR expression was also related to tumor grade, stage, age, and tumor status. Cell counting kit-8, Transwell, and wound healing assay showed that knocking out LYAR significantly inhibited the proliferation, migration, and invasion of hepatocellular carcinoma cells. In addition, this study found that LYARexpression was significantly positively correlated with MKI67IP, BZW2, and CCT2. Gene set enrichment analysis results showed that samples with high LYAR expression levels were rich in spliceosomes, RNA degradation, pyrimidine metabolism, cell cycle, nucleotide excision repair, and base excision repair.
引用
收藏
页码:9452 / 9462
页数:11
相关论文
共 22 条
[1]   Genome-Wide Gain-of-Function Screen Identifies Novel Regulators of Pluripotency [J].
Abujarour, Ramzey ;
Efe, Jem ;
Ding, Sheng .
STEM CELLS, 2010, 28 (09) :1487-1497
[2]   The multifunctional nucleolus [J].
Boisvert, Francois-Michel ;
van Koningsbruggen, Silvana ;
Navascues, Joaquin ;
Lamond, Angus I. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2007, 8 (07) :574-585
[3]   Splicing and cancer: Challenges and opportunities [J].
Coltri, Patricia P. ;
dos Santos, Maria G. P. ;
da Silva, Guilherme H. G. .
WILEY INTERDISCIPLINARY REVIEWS-RNA, 2019, 10 (03)
[4]   Hypermutation of DPYD Deregulates Pyrimidine Metabolism and Promotes Malignant Progression [J].
Edwards, Lauren ;
Gupta, Rohit ;
Filipp, Fabian Volker .
MOLECULAR CANCER RESEARCH, 2016, 14 (02) :196-206
[5]   The nucleolus: structure/function relationship in RNA metabolism [J].
Hernandez-Verdun, Daniele ;
Roussel, Pascal ;
Thiry, Marc ;
Sirri, Valentina ;
Lafontaine, Denis L. J. .
WILEY INTERDISCIPLINARY REVIEWS-RNA, 2010, 1 (03) :415-431
[6]   BZW2 promotes the malignant progression of colorectal cancer via activating the ERK/MAPK pathway [J].
Huang, Longping ;
Chen, Si ;
Fan, Haijun ;
Ai, Fan ;
Sheng, Weiwei .
JOURNAL OF CELLULAR PHYSIOLOGY, 2020, 235 (05) :4834-4842
[7]   Building an efficient factory: where is pre-rRNA synthesized in the nucleolus? [J].
Huang, S .
JOURNAL OF CELL BIOLOGY, 2002, 157 (05) :739-741
[8]   Interconnection between Metabolism and Cell Cycle in Cancer [J].
Icard, Philippe ;
Fournel, Ludovic ;
Wu, Zherui ;
Alifano, Marco ;
Lincet, Hubert .
TRENDS IN BIOCHEMICAL SCIENCES, 2019, 44 (06) :490-501
[9]   Whole genome expression profiling of blood cells in ovarian cancer patients -Prognostic impact of the CYP1B1, MTSS1, NCALD, and NOP14 genes [J].
Isaksson, Helena S. ;
Sorbe, Bengt ;
Nilsson, Torbjorn K. .
ONCOTARGET, 2014, 5 (12) :4040-4049
[10]   Role of the novel gene BZW2 in the development of hepatocellular carcinoma [J].
Jin, Xin ;
Liao, Mingmei ;
Zhang, Lihua ;
Yang, Manyi ;
Zhao, Jinfeng .
JOURNAL OF CELLULAR PHYSIOLOGY, 2019, 234 (09) :16592-16600