[1]沈华,盛晓鹃.HPV 阳性宫颈癌组织中IGF2BP2 和RPRD1B 的表达水平及临床价值研究[J].现代检验医学杂志,2023,38(05):121-126.[doi:10.3969/j.issn.1671-7414.2023.05.023]
 SHEN Hua,SHENG Xiaojuan.Expression and Clinical Value of IGF2BP2 and RPRD1B in HPV Positive Cervical Cancer Tissues[J].Journal of Modern Laboratory Medicine,2023,38(05):121-126.[doi:10.3969/j.issn.1671-7414.2023.05.023]
点击复制

HPV 阳性宫颈癌组织中IGF2BP2 和RPRD1B 的表达水平及临床价值研究()
分享到:

《现代检验医学杂志》[ISSN:/CN:]

卷:
第38卷
期数:
2023年05期
页码:
121-126
栏目:
论著
出版日期:
2023-09-15

文章信息/Info

Title:
Expression and Clinical Value of IGF2BP2 and RPRD1B in HPV Positive Cervical Cancer Tissues
文章编号:
1671-7414(2023)05-121-06
作者:
沈华盛晓鹃
(南通市海门区人民医院妇产科,江苏南通 226100)
Author(s):
SHEN Hua SHENG Xiaojuan
(Department of Obstetrics and Gynecology, Nantong Haimen District People’s Hospital, Jiangsu Nantong 226100, China)
关键词:
人乳头瘤病毒宫颈癌胰岛素样生长因子2 结合蛋白2细胞核前mRNA 结构域的调节因子1B
分类号:
R737.33;R730.43
DOI:
10.3969/j.issn.1671-7414.2023.05.023
文献标志码:
A
摘要:
目的 研究人乳头瘤病毒(human papilloma virus,HPV)阳性宫颈癌组织中胰岛素样生长因子2 结合蛋白2(insulin-like growth factor2 binding protein 2,IGF2BP2) 与细胞核前mRNA 结构域调节因子1B(regulatory nuclearpre-mRNA domain containing 1B,RPRD1B) 的表达及临床价值。方法 选取自2018 年1 月~ 2019 年1 月期间于南通市海门区人民医院诊治的82 例HPV 阳性宫颈癌患者的癌组织和癌旁组织,以41 例HPV 阴性宫颈癌组织为对照。应用免疫组织化学分析组织中IGF2BP2,RPRD1B 蛋白表达。Spearman 秩相关分析IGF2BP2 与RPRD1B 蛋白表达的相关性。Kaplan-Meier 生存分析IGF2BP2,RPRD1B 蛋白表达对生存预后的影响。COX 比例风险模型分析影响HPV 阳性宫颈癌患者生存预后的因素。结果 HPV 阳性癌组织IGF2BP2,RPRD1B 蛋白阳性率高于HPV 阴性癌组织(67.07% vs 9.76%,6.10%)及癌旁正常组织(70.73% vs 17.07%,7.32%),差异具有统计学意义(χ2=35.978,65.705;31.582,62.290,均P<0.05)。IGF2BP2 与RPRD1B 蛋白表达呈显著正相关(r=0.717,P<0.05)。肿瘤FIGO 分期Ⅱ A 期、伴淋巴结转移HPV 阳性宫颈癌组织中IGF2BP2(82.61%,90.63%),RPRD1B(86.95%,93.75%) 蛋白阳性率分别高于Ⅰ A ~Ⅰ B期(47.22%,52.00%)、无淋巴结转移组织(50.00%,56.00%),差异均具有统计学意义(χ2=11.450 ~ 13.432,均P< 0.05)。IGF2BP2 阳性组三年累积生存率低于IGF2BP2 阴性组(65.45% vs 88.89%)、RPRD1B 阳性组三年累积生存率低于RPRD1B 阴性组(65.32% vs 91.67%),差异具有统计学意义(Log Rank χ2=6.487,5.192,均P<0.05)。FIGO分期Ⅱ A 期(OR=1.579,95%CI=1.042 ~ 2.393)、并发淋巴结转移(OR=1.960,95%CI=1.180 ~ 3.256),IGF2BP2阳性(OR=1.786,95%CI=1.226 ~ 2.602)和RPRD1B 阳性(OR=1.602,95%CI=1.119 ~ 2.293)是影响HPV 阳性宫颈癌患者生存预后的独立危险因素。结论 宫颈癌中IGF2BP2 和RPRD1B 表达升高,两者与FIGO 分期、淋巴结转移有关,是影响HPV 阳性宫颈癌患者预后的独立危险因素。
Abstract:
Objective To study the expression and clinical significance of insulin-like growth factor 2 binding protein 2 (IGF2BP2) and regulatory nuclear pre-mRNA domain containing 1B (RPRD1B) in HPV-positive cervical cancer tissues. Methods From January 2018 to January 2019, 82 cases of HPV-positive cervical cancer tissues and paracancerous tissues collected in Nantong Haimen District People’s Hospital were selected as the study subjects, and 41 cases of HPV-negative cervical cancer tissues were selected as the control. Immunohistochemistry was used to analyze the expression of IGF2BP2 and RPRD1B protein in tissues. Spearman rank correlation analysis was used to analyze the correlation between IGF2BP2 and RPRD1B protein expression. Kaplan-Meier survival analysis was used to analyze the effect of IGF2BP2, RPRD1B protein expression on survival prognosis in HPV-positive cervical cancer patients. COX proportional risk model was used to analyze factors affecting the survival and prognosis of HPV positive cervical cancer patients. Results The positive rate of IGF2BP2 and RPRD1B protein in HPV-positive cancer tissue was significantly higher than that in HPV-negative cancer tissue(67.07% vs 9.76%, 6.10%) and adjacent normal tissue(70.73% vs 17.07%,7.32%), and the differences were statistically significant (χ2=35.978, 65.705; 31.582, 69.290, all P<0.05). IGF2BP2 was positively correlated with RPRD1B protein expression (r=0.717, P<0.05). The positive rates of IGF2BP2 (82.61% , 90.63%) and RPRD1B (86.95%, 93.75%) protein expression in cervical cancer tissues with FIGO stage IIA and HPV positive lymph node metastasis were higher than those in stage IA to stage IB (47.22%,52.00%)and tissues without lymph node metastasis(50.00%,56.00%),and the differences were statistically significant(χ2=11.450 ~ 13.432,all P < 0.05). The 3-year cumulative survival rates of patients in the IGF2BP2 positive expression group and RPRD1B positive expression group were lower than those in the IGF2BP2 negative expression group(65.45% vs 88.89%) and RPRD1B negative expression group(65.32% vs 91.67%), respectively (Log Rank χ2=6.487, 5.192,P<0.05). FIGO stage Ⅱ A (OR=1.579,95% CI=1.042 ~ 2.393), combined with lymph node metastasis (OR=1.960, 95% CI=1.180 ~ 3.256), IGF2BP2 positive (OR=1.786,95% CI=1.226 ~ 2.602), RPRD1B positive (OR=1.602,95% CI=1.119 ~ 2.293) were independent risk factors affecting the survival and prognosis of HPV-positive cervical cancer patients. Conclusion The increased expression of IGF2BP2 and RPRD1B in cervical cancer were related to FIGO stage and lymph node metastasis, and both of them were independent risk factors affecting the prognosis of HPV-positive cervical cancer patients.

参考文献/References:

[1] HE Wenqiang, LI Chenxi. Recent global burden of cervical cancer incidence and mortality, predictors, and temporal trends[J]. Gynecologic Oncology, 2021, 163(3): 583-592.
[2] 陈慎, 杜明君, 宋雅琴. 宫颈组织HPV DNA 与血清Chemerin,Leptin 水平联合检测对宫颈癌早期诊断的价值分析[J], 现代检验医学杂志, 2019, 34(3): 42-46. CHEN Shen, DU Mingjun, SONG Yaqin. Value of combined detection of HPV DNA and serum levels of chemerin and leptin in early diagnosis of cervical cancer[J]. Journal of Modern Laboratory Medicine, 2019, 34(3): 42-46.
[3] WANG Yun, LU Jiahuan, WU Qinian, et al. LncRNA LINRIS stabilizes IGF2BP2 and promotes the aerobic glycolysis in colorectal cancer[J]. Molecular Cancer, 2019, 18(1): 174.
[4] PU Jian, WANG Jianchu, QIN Zebang, et al. IGF2BP2 promotes liver cancer growth through an m6A-FEN1-dependent mechanism[J]. Frontiers in Oncology, 2020, 10: 578816.
[5] CUGUSI S, BAJPE P K, MITTER R, et al. An important role for RPRD1B in the heat shock response[J]. Molecular and Cellular Biology, 2022, 42(10): e0017322.
[6] JIA Yongxu, YAN Qian, ZHENG Yinli, et al. Long non-coding RNA NEAT1 mediated RPRD1B stability facilitates fatty acid metabolism and lymph node metastasis via c-Jun/c-Fos/SREBP1 axis in gastric cancer[J]. Journal of Experimental & Clinical Cancer Research, 2022, 41(1): 287.
[7] YU Yanqin, HAO Jinqi, MENDEZ M J G, et al. The prevalence of cervical HPV infection and genotype distribution in 856,535 Chinese women with normal and abnormal cervical lesions: a systemic review[J].Journal of Cytology / Indian Academy of Cytologists, 2022, 39(4): 137-147.
[8] WANG Jinyan, CHEN Lijuan, QIANG Ping. The role of IGF2BP2,an m6A reader gene,in human metabolic diseases and cancers[J]. Cancer Cell International, 2021, 21(1): 99.
[9] XU Xiaodong, YU Yan, ZONG Ke, et al. Up-regulation of IGF2BP2 by multiple mechanisms in pancreatic cancer promotes cancer proliferation by activating the PI3K/Akt signaling pathway[J]. Journal of Experimental & Clinical Cancer Research, 2019, 38(1): 497.
[10] JIANG Xingkang, GUO Shanqi, WANG Shuo, et al. EIF4A3-induced circARHGAP29 promotes aerobic glycolysis in docetaxel-resistant prostate cancer through IGF2BP2/c-Myc/LDHA signaling[J]. Cancer Research, 2022, 82(5): 831-845.
[11] HU Chenchen, LIU Tianyue, HAN Chenying, et al. HPV E6/E7 promotes aerobic glycolysis in cervical cancer by regulating IGF2BP2 to stabilize m6A-MYC expression[J]. International Journal of Biological Sciences, 2022, 18(2): 507-521.
[12] CUI Jie, TIAN Jiale, WANG Weiwei, et al. IGF2BP2 promotes the progression of colorectal cancer through a YAP-dependent mechanism[J]. Cancer Science, 2021, 112(10): 4087-4099.
[13] WU E Y, HUANG Liping, BAO Jinhua. MiR-96-5p regulates cervical cancer cell resistance to cisplatin by inhibiting LncRNA TRIM52-AS1 and promoting IGF2BP2[J]. Kaohsiung Journal of Medical Sciences, 2022, 38(12): 1178-1189.
[14] FENG Panpan, CHEN Dawei, WANG Xia, et al. Inhibition of the m(6)A reader IGF2BP2 as a strategy against T-cell acute lymphoblastic leukemia[J].Leukemia, 2022, 36(9): 2180-2188.
[15] LIANG Wenquan, XI Hongqing, LIU Yuhua, et al. MiR-139-5p inhibits the proliferation of gastric cancer cells by targeting Regulation of Nuclear PremRNA Domain Containing 1B[J]. Biochemical and Biophysical Research Communications, 2020, 527(2): 393-400.
[16] WEN Na, BIAN Lihua, GONG Jing, et al. Overexpression of cell-cycle related and expression-elevated protein in tumor (CREPT) in malignant cervical cancer[J].Journal of International Medical Research, 2020, 48(1): 300060519895089.
[17] WEN Na, BIAN Lihua, GON Jing, et al. RPRD1B is a potentially molecular target for diagnosis and prevention of human papillomavirus E6/E7 infectioninduced cervical cancer: a case-control study [J]. Asia-Pacific Journal of Clinical Oncology, 2021, 17(3): 230-237.
[18] ZHAI Wanli, YE Xiongjun, WANG Yinyin, et al. CREPT/RPRD1B promotes tumorigenesis through STAT3-driven gene transcription in a p300-dependent manner[J]. British Journal of Cancer, 2021, 124(8): 1437-1448.
[19] ZHANG Yanquan, LIU Chunxiao, DUAN Xiaolin, et al. CREPT/RPRD1B, a recently identified novel protein highly expressed in tumors, enhances the β-catenin·TCF4 transcriptional activity in response to Wnt signaling[J]. Journal of Biological Chemistry, 2014, 289(33): 22589-22599.
[20] YANG Gang, WANG Yicheng, XIAO Jianchun, et al. CREPT serves as a biomarker of poor survival in pancreatic ductal adenocarcinoma[J]. Cellular Oncology, 2021, 44(2): 345-355.

相似文献/References:

[1]孔倩倩a,唐振华,相芬芬a,等.抗HPV18 E6多肽单克隆抗体的制备及鉴定[J].现代检验医学杂志,2016,31(03):30.[doi:10.3969/j.issn.1671-7414.2016.03.009]
 KONG Qian-qiana,TANG Zhen-hua,XIANG Fen-fena,et al.Preparation and Identification of A Peptide Monoclonal Antibody Against Human Papillomavirus 18E6[J].Journal of Modern Laboratory Medicine,2016,31(05):30.[doi:10.3969/j.issn.1671-7414.2016.03.009]
[2]王 妍,黄钦贤,林章礼,等.汕头地区女性HPV的感染状况回顾[J].现代检验医学杂志,2015,30(04):122.[doi:10.3969/j.issn.1671-7414.2015.04.036]
 WANG Yan,HUANG Qin-xian,LIN Zhang-li,et al.Review of HPV Infection Status of the Women in Shantou Region[J].Journal of Modern Laboratory Medicine,2015,30(05):122.[doi:10.3969/j.issn.1671-7414.2015.04.036]
[3]田英,王双勇,赵雅,等.宫颈癌组织细胞中Numb基因表达及相关性研究[J].现代检验医学杂志,2015,30(06):42.[doi:10.3969/j.issn.1671-7414.2015.06.012]
 TIAN Ying,WANG Shuang-yong,ZHAO Ya,et al.Study on Correlation and Expression of Numb Gene in Cervical Cancer[J].Journal of Modern Laboratory Medicine,2015,30(05):42.[doi:10.3969/j.issn.1671-7414.2015.06.012]
[4]原荣,李军,王一羽,等.陕西省榆林地区和商洛地区HPV感染及亚型分布对比研究[J].现代检验医学杂志,2016,31(06):48.[doi:10.3969/j.issn.1671-7414.2016.06.013]
 YUAN Rong,LI Jun,WANG Yi-yu,et al.Study on HPV Infection Rate and Hypotype Distribution between Yulin and Shangluo Area in Shaanxi Province[J].Journal of Modern Laboratory Medicine,2016,31(05):48.[doi:10.3969/j.issn.1671-7414.2016.06.013]
[5]原 荣,李 军,南 星,等.陕西省安康和延安两地区妇女HPV感染及型别分布对比研究[J].现代检验医学杂志,2017,32(02):64.[doi:10.3969/j.issn.1671-7414.2017.02.017]
 YUAN Rong,LI Jun,NAN Xing,et al.Comparative Study on HPV Infection and Hypotype Distribution between Ankang and Yan'an Area of Shaanxi Province[J].Journal of Modern Laboratory Medicine,2017,32(05):64.[doi:10.3969/j.issn.1671-7414.2017.02.017]
[6]韩 伟a,刘文康b,翟卫斌c,等.西安地区男性尿道感染人乳头瘤病毒基因亚型分析[J].现代检验医学杂志,2017,32(03):52.[doi:10.3969/j.issn.1671-7414.2017.03.014]
 HAN Weia,LIU Wen-kangb,ZHAI Wei-binc,et al.Detection of Human Papillomavirus Subtypes in Male Urethra in Xi’an Area[J].Journal of Modern Laboratory Medicine,2017,32(05):52.[doi:10.3969/j.issn.1671-7414.2017.03.014]
[7]原 荣a,李 军a,南 星a,等.陕西省宝鸡和咸阳两地妇女HPV感染现状和类型分析[J].现代检验医学杂志,2017,32(06):145.[doi:10.3969/j.issn.1671-7414.2017.06.001]
 YUAN Ronga,LI Juna,NAN Xinga,et al.HPV Prevalence and Subtypes Analysis of Women in Baoji and Xianyang Area of Shaanxi Province[J].Journal of Modern Laboratory Medicine,2017,32(05):145.[doi:10.3969/j.issn.1671-7414.2017.06.001]
[8]顾益凤,朱自力,史跃燕,等.血浆硫氧还蛋白还原酶水平检测对宫颈癌早期诊断的价值研究[J].现代检验医学杂志,2019,34(02):40.[doi:10.3969/j.issn.1671-7414.2019.02.011]
 GU Yi-feng,ZHU Zi-li,SHI Yue-yan,et al.Study on the Value of Plasma Thioredoxin Reductase Levelin the Early Diagnosis of Cervical Cancer[J].Journal of Modern Laboratory Medicine,2019,34(05):40.[doi:10.3969/j.issn.1671-7414.2019.02.011]
[9]陈 慎,杜明君,宋雅琴.宫颈组织HPV DNA与血清Chemerin,Leptin水平联合检测对宫颈癌早期诊断的价值分析[J].现代检验医学杂志,2019,34(03):42.[doi:10.3969/j.issn.1671-7414.2019.03.010]
 CHEN Shen,DU Ming-jun,SONG Ya-qin.Value of Combined Detection of HPV DNA and Serum Levelsof Chemerin and Leptin in Early Diagnosis of Cervical Cancer[J].Journal of Modern Laboratory Medicine,2019,34(05):42.[doi:10.3969/j.issn.1671-7414.2019.03.010]
[10]周 静,李 智,周 玉,等.宫颈癌组织中 Ep-CAM和 Ki67的表达及临床意义[J].现代检验医学杂志,2019,34(06):24.[doi:10.3969 / j.issn.1671-7414.2019.06.006]
 ZHOU Jing,LI Zhi,ZHOU Yu,et al.Expression and Clinicd Value of Ep-CAM and Ki67 in the Cervial Carcinoma Tissue[J].Journal of Modern Laboratory Medicine,2019,34(05):24.[doi:10.3969 / j.issn.1671-7414.2019.06.006]

备注/Memo

备注/Memo:
基金项目:江苏省科学技术厅资助项目( 编号:20180537):高危型HPVE6/E7 蛋白在宫颈癌中的作用机制研究。
作者简介:沈华(1978-),女,本科,副主任医师,研究方向:妇产科临床,E-mail:shenhua53261@163.com。
通讯作者:盛晓鹃(1979-),女,本科,副主任医师,研究方向:妇产科临床。
更新日期/Last Update: 2023-09-15