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[1]胡 源,许戈良,荚卫东,等.C1QL1蛋白在原发性肝细胞癌中的表达及其临床意义[J].天津医科大学学报,2019,25(04):329-333.
 HU Yuan,XU Ge-liang,JIA Wei-dong,et al.Expressions of C1QL1 protein inprimaryhepatocellular carcinoma and its clinical significance[J].Journal of Tianjin Medical University,2019,25(04):329-333.
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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
25卷
期数:
2019年04期
页码:
329-333
栏目:
临床医学
出版日期:
2019-07-20

文章信息/Info

Title:
Expressions of C1QL1 protein inprimaryhepatocellular carcinoma and its clinical significance
文章编号:
1006-8147(2019)04-0329-05
作者:
胡 源1许戈良2荚卫东2潘婷婷2余继海2黄 玫3周杭城4
(1.天津医科大学研究生院,天津300070;2.中国科学技术大学附属第一医院(安徽省立医院)肝脏外科,合肥 230001;3.肝胆胰安徽省重点实验室,合肥230001;4.中国科学技术大学附属第一医院(安徽省立医院)病理科,合肥230001)
Author(s):
HU Yuan1 XU Ge-liang2 JIA Wei-dong2 PAN Ting-ting2 YU Ji-hai2 HUANG Mei3ZHOU Hang-cheng4
(1.Graduate School, Tianjin Medical University, Tianjin 300070, China; 2.Department of Hepatic Surgery, The First Affiliated Hospital, University of Science and Technology of China (Anhui Provincial Hospital),Hefei 230001, China; 3.Anhui Province Key Laboratory of Hepatopancreatobiliary Surgery, Hefei 230001, China; 4. Department of Pathology, The First Affiliated Hospital, University of Science and Technology of China (Anhui Provincial Hospital),Hefei 230001, China)
关键词:
肝细胞癌 C1QL1免疫组织化学Western blotqRT-PCR
Keywords:
hepatocellular carcinomaC1QL1immunohistochemistrywestern blotreal-time fluorescent qunatiative PCR
分类号:
R735.7
DOI:
-
文献标志码:
A
摘要:
目的:探讨C1QL1(C1q-like-1)蛋白在原发性肝细胞癌(HCC)中的表达及其临床意义。方法:采用免疫组织化学技术检测80例HCC组织中C1QL1蛋白的表达情况及其临床意义,用qRT-PCR及 Western blot 方法检测20对冷冻HCC组织及癌旁组织中C1QL1蛋白的表达。结果:80例石蜡组织标本的免疫组化结果显示,55例(68.8%)HCC组织中C1QL1蛋白呈高表达;而癌旁组织中8例(10%)C1QL1蛋白呈高表达,两组间表达差异具有统计学意义(P <0.001);C1QL1在HCC中的表达与有无乙肝病史(P=0.021)、肿瘤的大小(P=0.003)、血管侵犯(P=0.003)、TNM分期(P=0.002)及Edmondson分级(P=0.002)相关,而与年龄(P=0.758)、性别(P=0.672)、甲胎蛋白(AFP)(P=0.191)、肿瘤数目(P=0.877)、Child-Pugh分级(P=0.866)、肿瘤包膜完整程度(P=0.238)和肝硬化程度(P=0.316)均无关。qRT-PCR及Western blot 均显示HCC组织中C1QL1的表达量显著高于对应的癌旁组织,组间差异具有统计学意义( P<0. 01,P<0. 001) 。结论:在HCC组织中,C1QL1蛋白呈高表达,而C1QL1的高表达可能与HCC的发生发展及恶性程度密切相关。
Abstract:
Objective: To investigate the expression and clinical significance of C1QL1 in hepatocellular carcinoma (HCC). Methods:The expression level of C1QL1 in paraffin-embedded HCC tissues and adjacent tissues of HCC patients was measured by 80 cases of hepatectomy and postoperative pathology, and its relationship with clinicopathological was studied. Theq RT-PCR and Western blot were used to detect the expression of C1QL1 in 20 pairs of freshly frozen HCC and adjacent tissues. Results: Immunohistochemical results of paraffin tissue showed: the high expression rate of C1QL1 in HCC tissues was 68.8%(55/80), the high expression rate in adjacent tissues was 10%(8/80), and the expression difference between the two groups was statistically significant(P< 0.001). The expression of C1QL1 in HCC was correlated with the history of hepatitis B(P=0.021), tumor size(P=0.003), vascular invasion(P=0.003), TNM staging(P=0.002) and Edmondson classification (P=0.002), but was not correlated with age(P=0.758), sex(P=0.672), alpha fetoprotein(AFP)(P=0.191), the number of tumor(P=0.877), child-pugh classification(P=0.866), tumor envelope integrity(P=0.238) and degree of liver cirrhosis(P=0.316). BothqRT-PCR and Western blot showed that the expression of C1QL1 in HCC tissues was significantly higher than that in the corresponding paracancerous tissues, and the difference between the groups was statistically significant( P <0. 01,P <0. 001) . Conclusion:The expression of C1QL1 protein in HCC tissues is high.The high expression rate of C1QL1 may be closely related to the occurrence, progression and grade malignancy of hepatocellular carcinoma.

参考文献/References:


[1] El-Serag H B. Epidemiology of viral hepatitis and hepatocellular carcinoma[J]. Gastroenterology, 2012, 142(6): 1264
[2] Qiu X, Feng J R, Wang F, et al. Profiles of differentially expressed genes and overexpression of NEBL indicates a positive prognosis in patients with colorectal cancer[J]. Mol Med Rep, 2018, 17(2): 3028
[3] Celestino R, Nome T, Pestana A, et al. CRABP1, C1QL1 and LCN2 are biomarkers of differentiated thyroid carcinoma, and predict extrathyroidal extension[J]. BMC Cancer, 2018, 18(1):68
[4] Chun Y S, Pawlik T M, Vauthey J N. 8th Edition of the AJCC Cancer Staging Manual: Pancreas and Hepatobiliary Cancers[J]. Ann Surg Oncol, 2018, 25(4): 845
[5] Maréchal R, Demetter P, Nagy N, et al. High expression of CXCR4 may predict poor survival in resected pancreatic adenocarcinoma[J]. Briti J Cancer, 2009, 100(9): 1444
[6] 马杰,盛治勇,许戈良,等.CD90和CXCR4在肝癌中的表达及其与术后早期复发的关系[J].安徽医科大学学报,2016,51(1):129
[7] Edmondson H A, Steiner P E. Primary carcinoma of the liver: a study of 100 cases among 48,900 necropsies[J]. Cancer, 1954, 7(3):462
[8] Bruix J, Gores G J, Mazzaferro V. Hepatocellular carcinoma: clinical frontiers and perspectives[J]. Gut, 2014, 63(5): 844
[9] Chen W, Zheng R, Baade P D, et al. Cancer statistics in China, 2015[J]. CA Cancer J Clin, 2016, 66(2): 115
[10] Pascual S, Herrera I, Irurzun J. New advances in hepatocellular carcinoma[J]. World J Hepatol, 2016, 8(9): 421
[11] Ressl S, Vu B K, Vivona S, et al. Structures of C1q-like proteins reveal unique features among the C1q/TNF superfamily[J]. Structure, 2015, 23(4): 688
[12] Berube N G, Swanson X H, Bertram M J, et al. Cloning and characterization of CRF, a novel C1q-related factor, expressed in areas of the brain involved in motor function[J]. Brain Res Mol Brain Res, 1999, 63(2): 233
[13] Kakegawa W, Mitakidis N, Miura E, et al. Anterograde C1ql1 signaling is required in order to determine and maintain a single-winner climbing fiber in the mouse cerebellum[J]. Neuron, 2015, 85(2): 316
[14] Sigoillot S M, Iyer K, Binda F, et al. The Secreted Protein C1QL1 and Its Receptor BAI3 Control the Synaptic Connectivity of Excitatory Inputs Converging on Cerebellar Purkinje Cells[J]. Cell Rep, 2015, 10(5):820
[15] Yuzaki M. The C1q complement family of synaptic organizers: not just complementary[J]. Curr Opin Neurobiol, 2017, 45: 9

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备注/Memo

备注/Memo:
基金项目 国家自然科学基金资助项目(81501354)
作者简介 胡源(1993-),男,硕士在读;研究方向:肝肿瘤专题研究;通信作者:许戈良, E-mail:ahsyxgl@163.com。
更新日期/Last Update: 2019-08-28