META-ANALYSIS OF THE CORRELATION BETWEEN HIGH EXPRESSION OF LNCRNA NEAT1 IN RECTAL CANCER AND PATHOLOGICAL FEATURES AND PROGNOSIS

被引:0
作者
Lin, Qiyi [1 ]
Pan, Jianpeng [1 ]
Wang, Huaishuai [1 ]
Li, Yinlin [1 ]
Zhuang, Yixiang [1 ]
Cai, Zhicong [1 ]
Lin, Gaofeng [1 ]
Liu, Weibo [1 ]
Xu, Guoxi [1 ]
机构
[1] Jinjiang Municipal Hosp, Dept Gastrointestinal Surg, 16 Jinguang Rd,Luoshan St, Quanzhou 362200, Fujian, Peoples R China
关键词
lncRNA NEAT1; prognosis; rectal cancer; meta; COLORECTAL-CANCER; METASTASIS;
D O I
10.5937/jomb0-47889
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
Background: To systematically evaluate the relationship between the expression level of long noncoding RNA NEAT1 and the clinical characteristics and prognostic value of rectal cancer patients. Methods: PubMed, EMBASE, Cochrane library database and case -control studies on the correlation between abnormal expression of lncRNA NEAT1 and prognosis of rectal cancer patients published by the American clinical trials registry before May 1, 2023 were searched. The search time was from the establishment of the database to May 30, 2023. Results: A total of 7 case -control studies were included, including 1063 cancer patients. The results of meta -analysis showed that the high expression of lncRNA NEAT1 was significantly correlated with the degree of differentiation [or=0.45, 95%CI=0.32-0.63, P<0.01 ], tumor size [or=0.59, 95%CI=0.42-0.82, P<0.01 ], and overall survival [HR=1.34, 95%CI=1.21-1.48, P<0.001 ]; However, it was not associated with gender [or=1.23, 95%CI= 0.88-1.72, P=0.23 ] and lymph node metastasis [or=0.87, 95%CI=0.45-1.66, P=0.67 ]. Conclusions: The high expression of lncRNA NEAT1 may be a risk factor for poor prognosis in patients with malignant tumors, and lncRNA NEAT1 can be used as a biomarker to evaluate its
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页码:503 / 511
页数:9
相关论文
共 19 条
[1]   Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries (vol 68, pg 394, 2018) [J].
Bray, F. ;
Ferlay, J. ;
Soerjomataram, I ;
Siegel, R. L. ;
Torre, L. A. ;
Jemal, A. .
CA-A CANCER JOURNAL FOR CLINICIANS, 2020, 70 (04) :313-313
[2]  
[Anonymous], 2020, CA Cancer J Clin, V70, P313, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[3]  
Feng YG, 2020, AM J CANCER RES, V10, P237
[4]  
Guo T, 2020, AM J TRANSL RES, V12, P4542
[5]   The Cochrane Collaboration's tool for assessing risk of bias in randomised trials [J].
Higgins, Julian P. T. ;
Altman, Douglas G. ;
Gotzsche, Peter C. ;
Jueni, Peter ;
Moher, David ;
Oxman, Andrew D. ;
Savovic, Jelena ;
Schulz, Kenneth F. ;
Weeks, Laura ;
Sterne, Jonathan A. C. .
BMJ-BRITISH MEDICAL JOURNAL, 2011, 343
[6]   A screen for nuclear transcripts identifies two linked noncoding RNAs associated with SC35 splicing domains [J].
Hutchinson, John N. ;
Ensminger, Alexander W. ;
Clemson, Christine M. ;
Lynch, Christopher R. ;
Lawrence, Jeanne B. ;
Chess, Andrew .
BMC GENOMICS, 2007, 8 (1)
[7]   MALAT-1, a novel noncoding RNA, and thymosin β4 predict metastasis and survival in early-stage non-small cell lung cancer [J].
Ji, P ;
Diederichs, S ;
Wang, WB ;
Böing, S ;
Metzger, R ;
Schneider, PM ;
Tidow, N ;
Brandt, B ;
Buerger, H ;
Bulk, E ;
Thomas, M ;
Berdel, WE ;
Serve, H ;
Müller-Tidow, C .
ONCOGENE, 2003, 22 (39) :8031-8041
[8]   ANEMIA OF INFLAMMATION IN PATIENTS WITH COLORECTAL CANCER: CORRELATION WITH INTERLEUKIN-1, INTERLEUKIN-33 AND GALECTIN-1 [J].
Jocic, Miodrag ;
Arsenijevic, Nebojsa ;
Gajovic, Nevena ;
Jurisevic, Milena ;
Jovanovic, Ivan ;
Jovanovic, Milan ;
Zdravkovic, Natasa ;
Maric, Veljko ;
Jovanovic, Marina .
JOURNAL OF MEDICAL BIOCHEMISTRY, 2022, 41 (01) :79-90
[9]   Involvement of the long noncoding RNA NEAT1 in carcinogenesis [J].
Klec, Christiane ;
Prinz, Felix ;
Pichler, Martin .
MOLECULAR ONCOLOGY, 2019, 13 (01) :46-60
[10]   NEAT expression is associated with tumor recurrence and unfavorable prognosis in colorectal cancer [J].
Li, Yunlong ;
Li, Yaohui ;
Chen, Wenping ;
He, Fenfei ;
Tan, Zhaobang ;
Zheng, Jianyong ;
Wang, Weizhong ;
Zhao, Qingchuan ;
Li, Jipeng .
ONCOTARGET, 2015, 6 (29) :27641-27650