[1]郑葆龙,肖绍文.CT23基因在脑肿瘤中的表达情况及临床价值[J].医学信息,2020,33(05):94-96.[doi:10.3969/j.issn.1006-1959.2020.05.028]
 ZHENG Bao-long,XIAO Shao-wen.CT23 Gene Expression in Brain Tumors and its Clinical Value[J].Medical Information,2020,33(05):94-96.[doi:10.3969/j.issn.1006-1959.2020.05.028]
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CT23基因在脑肿瘤中的表达情况及临床价值()
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医学信息[ISSN:1006-1959/CN:61-1278/R]

卷:
33卷
期数:
2020年05期
页码:
94-96
栏目:
论著
出版日期:
2020-03-01

文章信息/Info

Title:
CT23 Gene Expression in Brain Tumors and its Clinical Value
文章编号:
1006-1959(2020)05-0094-03
作者:
郑葆龙肖绍文
(广西医科大学第一附属医院神经外科,广西 南宁 530021)
Author(s):
ZHENG Bao-longXIAO Shao-wen
(Department of Neurosurgery,the First Affiliated Hospital of Guangxi Medical University,Nanning 530021,Guangxi,China)
关键词:
CT23基因脑肿瘤癌-睾丸抗原逆转录聚合酶链反应
Keywords:
CT23 geneBrain tumorCancer-testis antigenReverse transcription polymerase chain reaction
分类号:
R739.4
DOI:
10.3969/j.issn.1006-1959.2020.05.028
文献标志码:
A
摘要:
目的 检测和明确癌-睾丸相关抗原(CTA)CT23基因在人脑肿瘤中的表达情况,评估该基因潜在的临床价值。方法 收集广西医科大学第一附属医院神经外科14例颅脑肿瘤病理标本,包括星形细胞瘤5例,髓母细胞瘤4例,胶质母细胞瘤5例,使用RT-PCR技术检测CT23基因在不同病理类型的脑肿瘤中的表达情况,比较其在不同类型脑肿瘤中的表达差异。结果 14例脑肿瘤样本中13例CT23表达阳性,其中星形细胞瘤4例,胶质母细胞瘤5例,髓母细胞瘤4例,CT23基因在三类脑肿瘤样本中的表达比较,差异无统计学意义(P>0.05)。结论 CT23基因作为一种肿瘤相关的基因,可表达于多种类型的人类脑肿瘤中,另外该基因的表达与脑肿瘤的发生、发展可能有关。
Abstract:
Objective To detect and clarify the expression of the cancer-testis-associated antigen (CTA) CT23 gene in human brain tumors, and to evaluate its potential clinical value. Methods Collected 14 cases of craniocerebral tumor pathological specimens from Neurosurgery Department of the First Affiliated Hospital of Guangxi Medical University, including 5 cases of astrocytoma, 4 cases of medulloblastoma, and 5 cases of glioblastoma. RT-PCR was used to detect the expression of CT23 gene in brain tumors of different pathological types, and to compare the expression difference of CT23 gene in different types of brain tumors.Results The CT23 gene expression was positive in 13 of 14 brain tumor samples, including 4 astrocytomas, 5 glioblastomas, and 4 medullary tumors. Comparison of CT23 gene expression in three types of brain tumor samples, the difference was not statistically significant (P>0.05).Conclusion As a tumor-related gene, CT23 gene can be expressed in many types of human brain tumors. In addition, the expression of this gene may be related to the occurrence and development of brain tumors.

参考文献/References:

[1]Smith JS,Chang EF,Lamborn KR,et al.Role of extent of resection in the long-term outcome of low-grade hemispheric gliomas[J].Journal of Clinical Oncology,2008,26(8):1338-1345.[2]Randomized Trial on the efficacy of Radiotherapy for Cerebral Low-Grade Glioma in the Adult:European Organization for Research and Treatment of Cancer Study 22845 with the Medical Research Council Study BR04:An Interim Analysis[J].International Journal of Radiation Oncology Biology Physics,2002,52(2):316-324.[3]Popova SN,Bergqvist M,Dimberg A,et al.Subtyping of gliomas of various WHO grades by the application of immunohistochemistry[J].Histopathology,2014,64(3):365-379.[4]Whitehurst AW.Tumor antigen acrosin binding protein normalizes mitotic spindle function to promote cancer cell proliferation[J].Cancer Research,2010,70(19):7652-7661.[5]Fan R,Huang W,Luo B,et al.Cancer testis antigen OY-TES-1:analysis of protein expression in ovarian cancer with tissue microarrays[J].European Journal of Gynaecological Oncology,2015,36(3):298-303.[6]Luo B,Yun X,Fan R,et al.Cancer testis antigen OY-TES-1 expression and serum immunogenicity in colorectal cancer:its relationship to clinicopathological parameters[J].International Journal of Clinical&Experimental Pathology,2013,6(12):2835-2845.[7]Hu Q,Fu J,Luo B,et al.OY-TES-1 may regulate the malignant behavior of liver cancer via NANOG, CD9,CCND2 and CDCA3:A bioinformatic analysis combine with RNAi and oligonucleotide microarray[J].Oncology Reports,2015,33(4):1965-1975.[8]Tammela J,Uenaka A,Ono T,et al.OY-TES-1 expression and serum immunoreactivity in epithelial ovarian cancer[J].International Journal of Oncology,2006,29(4):903-910.[9]Li X,Yan J,Fan R,et al.Serum immunoreactivity of cancer/testis antigen OY-TES-1 and its tissues expression in glioma[J].Oncology Letters,2017,13(5):3080-3086..[10]Dube C.The Proacrosin Binding Protein,sp32,Is Tyrosine Phosphorylated During Capacitation of Pig Sperm[J].Journal of Andrology,2005,26(4):519-528.[11]Fagerberg L,Hallstr?m BM,Oksvold P,et al.Analysis of the Human Tissue-specific Expression by Genome-wide Integration of Transcriptomics and Antibody-based Proteomics[J].Molecular&Cellular Proteomics,2014,13(2):397-406.[12]Ono T,Kurashige T,Harada N,et al.Identification of proacrosin binding protein sp32 precursor as a human cancer/testis antigen[J].Proceedings of the National Academy of Sciences,2001,98(6):3282-3287.[13]谢学成,邱海,汤帆,等.端粒酶逆转录酶在结直肠癌组织中的表达及其临床意义[J].中国癌症防治杂志,2014,6(3):252-257.[14]Luo Y,Liang F,Zhang ZY.PRL1 Promotes Cell Migration and Invasion by Increasing MMP2 and MMP9 Expression through Src and ERK1/2 Pathways\r[J].Biochemistry,2009,48(8):1838-1846.[15]Fu J,Luo B,Guo W,et al.Down-regulation of cancer/testis antigen OY-TES-1 attenuates malignant behaviors of hepatocellular carcinoma cells in vitro[J].International Journal of Clinical&Experimental Pathology,2015,8(7):7786.[16]Cen YH,Guo WW,Luo B,et al.Knockdown of OY-TES-1 by RNAi causes cell cycle arrest and migration decrease in bone marrow-derived mesenchymal stem cells[J].Cell Biology International,2012,36(10):917-922.[17]Groff JL,Rutkowski RB,Brantley NB.Automation of a kinetic method for determiningangiotensin-converting enzyme in serum[J].Clinical Chemistry,1995,41(11):1662-1663.[18]Okumura H,Noguchi Y,Uenaka A,et al.Identification of an HLA-A24-Restricted OY-TES-1 Epitope Recognized by Cytotoxic T-Cells[J].Microbiology and Immunology,2005,49(11):1009-1016.[19]Karen SA,Joshua L.The Sentinel Within:Exploiting the Immune System for Cancer Biomarkers[J].Journal of Proteome Research,2005(4):1123-1133.[20]He SJ,Gu YY,Yu L,et al.High expression and frequently humoral immune response of melanoma-associated antigen D4 in glioma[J].International Journal of Clinical and Experimental Pathology,2014,7(5):2350-2360.[21]Laidi F,Bouziane A,Errachid A,et al.Usefulness of Salivary and Serum Auto-antibodies Against Tumor Biomarkers HER2 and MUC1 in Breast Cancer Screening[J].Asian Pacific Journal of Cancer Prevention,2016,17(1):335-339.

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更新日期/Last Update: 2020-03-01