[1]安立娟,张 翔,庞学成,等.子宫内膜癌组织中LGALS3BP mRNA,G3BP1 mRNA的表达与Wnt/β-catenin通路基因及临床病理学特征的相关性研究[J].现代检验医学杂志,2025,40(04):43-49.[doi:10.3969/j.issn.1671-7414.2025.04.008]
 AN Lijuan,ZHANG Xiang,PANG Xuecheng,et al.Expression of LGALS3BP mRNA, G3BP1 mRNA in Endometrial Cancer Tissue and Their Correlation with the Wnt/β-catenin Pathway Genes and Clinical Pathological Characteristics[J].Journal of Modern Laboratory Medicine,2025,40(04):43-49.[doi:10.3969/j.issn.1671-7414.2025.04.008]
点击复制

子宫内膜癌组织中LGALS3BP mRNA,G3BP1 mRNA的表达与Wnt/β-catenin通路基因及临床病理学特征的相关性研究()

《现代检验医学杂志》[ISSN:/CN:]

卷:
第40卷
期数:
2025年04期
页码:
43-49
栏目:
论著
出版日期:
2025-07-15

文章信息/Info

Title:
Expression of LGALS3BP mRNA, G3BP1 mRNA in Endometrial Cancer Tissue and Their Correlation with the Wnt/β-catenin Pathway Genes and Clinical Pathological Characteristics
文章编号:
1671-7414(2025)04-043-07
作者:
安立娟张 翔庞学成钱素敏杨伟伟
(沧州市中心医院妇科,河北沧州 061000)
Author(s):
AN Lijuan, ZHANG Xiang, PANG Xuecheng, QIAN Sumin, YANG Weiwei
(Department of Gynaecology, Cangzhou Central Hospital, Hebei Cangzhou 061000, China)
关键词:
子宫内膜癌半乳糖凝集素-3 结合蛋白GTP 酶激活蛋白SH3 功能区结合蛋白1Wnt/β-catenin通路
分类号:
R737.33;R730.43
DOI:
10.3969/j.issn.1671-7414.2025.04.008
文献标志码:
A
摘要:
目的 探讨子宫内膜癌(EC)组织中半乳糖凝集素-3 结合蛋白(LGALS3BP)、GTP 酶激活蛋白SH3 功能区结合蛋白1(G3BP1)表达与Wnt/β-catenin 通路基因的相关性及临床预后意义。方法 选择2016 年2 月~2019 年2月沧州市中心医院诊治的138 例EC 患者。采用实时荧光定量PCR(qRT-PCR) 检测癌和癌旁组织LGALS3BP mRNA,G3BP1 mRNA 及Wnt/β-catenin 通路基因Wnt5a mRNA,β-catenin mRNA,基质金属蛋白酶-9(MMP-9)mRNA 表达。采用免疫组织化学法(IHC) 检测癌和癌旁组织LGALS3BP 蛋白、G3BP1 蛋白表达。Pearson 相关分析LGALS3BPmRNA,G3BP1 mRNA 及Wnt/β-catenin 通路基因的相关性。利用Kaplan-Meier 曲线分析LGALS3BP mRNA,G3BP1mRNA 对EC 患者生存预后的影响。COX 回归模型分析影响EC 患者预后的因素。结果 EC 癌组织中 LGALS3BPmRNA(3.01±0.34),G3BP1 mRNA(2.87±0.33),Wnt5a mRNA(2.29±0.26),β-catenin mRNA(3.25±0.41),MMP-9 mRNA(2.68±0.36) 表达均高于癌旁组织(1.10±0.23,1.06±0.24,0.84±0.17,0.88±0.26,0.69±0.17),差异具有统计学意义(t=52.109 ~ 58.719,均P < 0.001)。EC 中LGALS3BP mRNA,G3BP1 mRNA 与Wnt5a mRNA,β-cateninmRNA,MMP-9 mRNA 表达呈正相关(r=0.675 ~ 0.781,均P < 0.001)。EC 癌组织中LGALS3BP 蛋白(3.54±0.47),G3BP1 蛋白(2.84±0.44)表达高于癌旁组织(0.51±0.16,0.42±0.13),差异具有统计学意义(t=71.692,61.962,均P < 0.001)。FIGO 分期Ⅲ期、淋巴结转移EC 患者癌组织LGALS3BP mRNA,G3BP1 mRNA 表达高于FIGO 分期Ⅰ ~ Ⅱ期、无淋巴结转移患者,差异具有统计学意义(t=40.279 ~ 557.671,均P <0.001)。LGALS3BP mRNA 高表达组5 年生存率为58.82%(40/68),低于低表达组的94.29%(66/70),差异具有统计学意义(Log-rank χ2=24.970,P< 0.001);G3BP1 mRNA 高表达组5 年生存率为62.12%(41/66),低于低表达组的90.28%(65/72),差异具有统计学意义(Log-rankχ2=15.960,P < 0.001)。FIGO 分期Ⅲ期、淋巴结转移、LGALS3BP mRNA 高表达、G3BP1 mRNA 高表达是EC 患者不良预后的危险因素(Wald χ2=7.847~12.054,均P<0.001)。结论 EC 中LGALS3BP,G3BP1 mRNA 表达升高,两者均与Wnt/β-catenin 通路基因表达呈正相关,促进EC 肿瘤的恶性进展,是新的评估EC 患者预后的肿瘤标志物。
Abstract:
Objective To investigate the correlation between the expression of lectin galactoside binding soluble-3 binding protein (LGALS3BP), GTP enzyme activating protein SH3 functional region binding protein 1(G3BP1) and Wnt / β-catenin pathway genes in endometrial cancer (EC) tissues and its clinical prognostic significance. Methods 138 patients with EC treated in Cangzhou Central Hospital from February 2016 to February 2019 were selected. qRT-PCR was used to detect the expression of LGALS3BP mRNA, G3BP1 mRNA and Wnt / β-catenin pathway genes Wnt5a mRNA, β-catenin mRNA and matrix metalloproteinase-9 (MMP-9) mRNA in cancer and adjacent tissues.The expression of LGALS3BP protein and G3BP1 protein in cancer and adjacent tissues was detected by immunohistochemistry.Pearson correlation analysis was used to analyze the correlation between LGALS3BP mRNA, G3BP1 mRNA and Wnt / β-catenin pathway genes.Kaplan-Meier curve was used to analyze the effect of LGALS3BP mRNA and G3BP1 mRNA on the survival and prognosis of EC patients. COX regression model was used to analyze the factors affecting the prognosis of EC patients. Results The expression of LGALS3BP mRNA(3.01± 0.34), G3BP1 mRNA(2.87±0.33), Wnt5a mRNA(2.29±0.26), β-catenin mRNA(3.25±0.41) and MMP-9 mRNA(2.68±0.36) in EC cancer tissues were higher than those in adjacent tissues(1.10±0.23,1.06±0.24,0.84±0.17,0.88±0.26,0.69±0.17), and the differences were statistically significant (t = 52.109 ~ 58.719, all P < 0.001).The expression of LGALS3BP mRNA and G3BP1 mRNA in EC was positively correlated with the expression of Wnt5a mRNA, β-catenin mRNA and MMP-9 mRNA (r = 0.675~0.781, all P < 0.001).The expression of LGALS3BP protein (3.54 ± 0.47 vs 0.51 ± 0.16) and G3BP1 protein (2.84 ± 0.44 vs 0.42 ± 0.13) in EC cancer tissues were higher than that in adjacent tissues, and the differences were statistically significant (t = 71.692,61.962, all P < 0.001).The expression of LGALS3BP mRNA and G3BP1 mRNA in cancer tissues of EC patients with FIGO stage III and lymph node metastasis were higher than that of FIGO stage I ~ II and no lymph node metastasis, and the differences were statistically significant (t = 40.279 ~ 557.671, all P < 0.001).The 5-year survival rate of LGALS3BP mRNA high expression group was 58.82 % (40 / 68), which was lower than that of low expression group 94.29 % (66 / 70), and the difference was statistically significant (Log-rank χ2 = 24.970, P < 0.001).The 5-year survival rate of G3BP1 mRNA high expression group was 62.12 % (41 / 66), which was lower than that of low expression group 90.28 % (65 / 72), and the difference was statistically significant (Log-rank χ2= 15.960, P < 0.001).FIGO stage III, lymph node metastasis, high expression of LGALS3BP mRNA and high expression of G3BP1 mRNA were risk factors for poor prognosis of EC patients (Wald χ2=7.847~12.054,all P < 0.001). Conclusion The expression of LGALS3BP and G3BP1 mRNA is elevated in EC, both of which are associated with Wnt/ β- catenin pathway genes, promoting the malignant progression of EC tumors, and are new tumor markers for evaluating the prognosis of EC patients.

参考文献/References:

[1] CROSBIE E J, KITSON S J, MCALPINE J N, et al. Endometrial cancer[J]. Lancet (London, England),2022,399(10333):1412-1428.
[2] 中国抗癌协会妇科肿瘤专业委员会. 子宫内膜癌诊断与治疗指南(2021 年版)[J]. 中国癌症杂志,2021,31(6):501-512. Gynecologic Oncology Committee of Chinese Anti-Cancer Association. Guidelines for diagnosis and treatment of endometrial cancer (2021 edition)[J]. China Oncology,2021,31(6):501-512.
[3] 张红雨, 陆奉科, 李山, 等. 子宫内膜癌患者血清CA125 水平与外周血RDW 检测在临床病理分期中的应用价值[J]. 现代检验医学杂志,2020,35(1):94-96,100. ZHANG H Y, LU F K, LI S,et al. Value of serum CA125 level and peripheral blood RDW detectionin clinical pathological staging of patients with endometrial cancer[J]. Journal of Modern Laboratory Medicine, 2020,35(1): 94-96, 100.
[4] FAUSTINI F, IDBORG H, FUZZI E, et al. Urine Galectin-3 binding protein reflects nephritis activity in systemic lupus erythematosus[J].Lupus,2023,32(2):252-262.
[5] LIU Y, LIANG L, LI J, et al. Aberrant expression of LGALS3BP drives an unfavorable prognosis and more aggressive in HCC via regulating PI3K/AKT signaling[J]. Tissue & Cell, 2024, 89:102471.
[6] GUTI?RREZ-GARCIA R, KOYUNCU S, HOMMEN F, et al. G3BP1-dependent mechanism suppressing protein aggregation in Huntington’s models and its demise upon stress granule assembly[J]. Human Molecular Genetics, 2023,32(10):1607-1621.
[7] GE Y D, JIN J B, LI J Y, et al. The roles of G3BP1 in human diseases (review)[J]. Gene, 2022,821:146294.
[8] 李儒彩, 黄成谋, 林道锐, 等. 解整合素金属蛋白酶10 通过介导Wnt/β-catenin 信号通路促进子宫内膜癌细胞上皮- 间质转化[J]. 现代肿瘤医学,2023,31(5):822-827. LI R C, HUANG C M, LIN D R, et al. A disintegrin and metalloproteinase 10 promotes epithelial-mesenchymal transition of endometrial cancer cells by mediating the Wnt/β-catenin signaling pathway[J]. Journal of Modern Oncology, 2023, 31 (5): 822-827.
[9] LU K H, BROADDUS R R. Endometrial Cancer[J]. the New England Journal of Medicine, 2020,383(21):2053-2064.
[10] KARPEL H, SLOMOVITZ B, COLEMAN R L, et al. Biomarker-driven therapy in endometrial cancer[J]. International Journal of Gynecological Cancer,2023,33(3):343-350.
[11] GUO K X, SHI J Y, TANG Z, et al. Circular RNA circARHGEF28 inhibited the progression of prostate cancer via the miR-671-5p/LGALS3BP/NF-κB axis[J]. Cancer Science, 2023,114(7):2907-2919.
[12] SONG Y F, WANG M F, TONG H, et al. Plasma exosomes from endometrial cancer patients contain LGALS3BP to promote endometrial cancer progression[J]. Oncogene, 2021, 40(3):633-646.
[13] KIMURA R, YOSHIMARU T, MATSUSHITA Y, et al. The GALNT6-LGALS3BP axis promotes breast cancer cell growth[J]. International Journal of Oncology,2020,56(2):581-595.
[14] ZHAO C Y, LIU Y S, MENG J Y, et al. LGALS3BP in microglia promotes retinal angiogenesis through PI3K/AKT pathway during hypoxia[J]. Investigative Ophthalmology & Visual Science, 2022,63(8):25.
[15] HONG C L, YU I S, PAI C H, et al. CD248 regulates Wnt signaling in pericytes to promote angiogenesis and tumor growth in lung cancer[J]. Cancer Research,2022,82(20):3734-3750.
[16] LUO M Y, ZHANG Q, HU Y C, et al. LGALS3BP: a potential plasma biomarker associated with diagnosis and prognosis in patients with sepsis[J]. Infection and Drug Resistance, 2021, 14: 2863-2871.
[17] CHEN X J, XUE Y T, WANG L F, et al. Lectin galactoside-binding soluble 3 binding protein mediates methotrexate resistance in choriocarcinoma cell lines[J]. Bioengineered, 2022,13(2):2076-2086.
[18] LIU S, TIAN S P, LIN T Y, et al. G3BP1 regulates breast cancer cell proliferation and metastasis by modulating PKCζ[J]. Frontiers in Genetics, 2022,13:1034889.
[19] GE Y D, JIN J B, CHEN G, et al. Endometrial cancer (EC) derived G3BP1 overexpression and mutant promote EC tumorigenesis and metastasis via SPOP/ERα axis[J]. Cell Communication and Signaling, 2023,21(1):303.
[20] JIANG W J, WANG J F, YANG X, et al. KIF14 promotes proliferation, lymphatic metastasis and chemoresistance through G3BP1/YBX1 mediated NF-κB pathway in cholangiocarcinoma[J]. Oncogene, 2023,42(17):1392-1404.
[21] ZHENG X C, CHEN J W, DENG M H, et al. G3BP1 and SLU7 jointly promote immune evasion by downregulating MHC-I via PI3K/AKT activation in bladder cancer[J]. Advanced Science (Weinheim, Baden-Württemberg, Germany), 2024,11(7):e2305922.
[22] ZHANG L N, ZHAO L, YAN X L, et al. Loss of G3BP1 suppresses proliferation, migration, and invasion of esophageal cancer cells via Wnt/β-catenin and PI3K/AKT signaling pathways[J]. Journal of Cellular Physiology, 2019,234(11):20469-20484.
[23] LI Y Z, WANG J D, ZHONG S, et al. Overexpression of G3BP1 facilitates the progression of colon cancer by activating β-catenin signaling[J]. Molecular Medicine Reports, 2020,22(5):4403-4411.
[24] ZHAO P, YUAN F, XU L J, et al. HKDC1 reprograms lipid metabolism to enhance gastric cancer metastasis and cisplatin resistance via forming a ribonucleoprotein complex[J]. Cancer Letters, 2023,569:216305.
[25] ZHAO J J, FU X H, CHEN H, et al. G3BP1 interacts with YWHAZ to regulate chemoresistance and predict adjuvant chemotherapy benefit in gastric cancer[J]. British Journal of Cancer, 2021,124(2):425-436.

相似文献/References:

[1]李 玲,罗雅文,何 霞,等.子宫内膜癌患者BMI与血清HE4,CA125联合检测的诊断价值[J].现代检验医学杂志,2018,33(05):91.[doi:10.3969/j.issn.1671-7414.2018.05.024]
 LI Ling,LUO Ya-wen,HE Xia,et al.Diagnostic Value of Combined Detection of Body Mass Index and Serum HE4,CA125 in Patients with Endometrial Carcinoma[J].Journal of Modern Laboratory Medicine,2018,33(04):91.[doi:10.3969/j.issn.1671-7414.2018.05.024]
[2]李晓丽,胡陇娟.子宫内膜癌组织中长链非编码RNA ZEB1-AS1的表达与临床特征及对化疗药物耐药性研究[J].现代检验医学杂志,2019,34(04):35.[doi:10.3969/j.issn.1671-7414.2019.04.009]
 LI Xiao-li,HU Long-juan.Research on Expression and Clinical Characteristics of Long-Chain Non-Coding RNA ZEB1-AS1 in Endometrial Carcinoma and Resistance to Chemotherapy Drugs[J].Journal of Modern Laboratory Medicine,2019,34(04):35.[doi:10.3969/j.issn.1671-7414.2019.04.009]
[3]王娟,刘鑫,席稳燕.HMMR-AS1 在子宫内膜癌化疗耐药中的作用[J].现代检验医学杂志,2020,35(05):45.[doi:10.3969/j.issn.1671-7414.2020.05.012]
 WANG Juan,LIU Xin,XI Wen-yan.Effect of HMMR-AS1 on the Chemotherapy-Resistance of Endometrial Cancer[J].Journal of Modern Laboratory Medicine,2020,35(04):45.[doi:10.3969/j.issn.1671-7414.2020.05.012]
[4]李功娟,张治洋,樊阳阳.FEZF1-AS1在子宫内膜癌中的表达及其与患者临床特征的相关性[J].现代检验医学杂志,2021,36(01):77.[doi:10.3969/j.issn.1671-7414.2021.01.020]
 LI Gong-juan,ZHANG Zhi-yang,FAN Yang-yang.Expression of FEZF1-AS1 in Endometrial Carcinoma and Its Correlation with Clinical Characteristics of Patients[J].Journal of Modern Laboratory Medicine,2021,36(04):77.[doi:10.3969/j.issn.1671-7414.2021.01.020]
[5]陈丽华,朱婕曼,刘玉凤,等.子宫内膜癌组织中血管紧张素~1-7及线粒体组装受体水平表达与临床病理特征的相关性[J].现代检验医学杂志,2021,36(02):24.[doi:doi:10.3969/j.issn.1671-7414.2021.02.006]
 CHEN Li-hua,ZHU Jie-man,LIU Yu-feng,et al.Correlation between the Expression of Angiotensin (1-7) and Mitochondrial Assembled Receptors and Clinicopathological Characteristics in Endometrial Cancer[J].Journal of Modern Laboratory Medicine,2021,36(04):24.[doi:doi:10.3969/j.issn.1671-7414.2021.02.006]
[6]陈晓宇,曾庆维,陈红林,等.子宫内膜癌组织中miR-3188和mTOR表达量与预后的相关性研究[J].现代检验医学杂志,2021,36(06):17.[doi:10.3969/j.issn.1671-7414.2021.06.004]
 CHEN Xiao-yu,ZENG Qing-wei,CHEN Hong-lin,et al.Study on the Correlation between the Expression Levels of miR-3188 and mTOR in Endometrial Cancer and the Prognosis[J].Journal of Modern Laboratory Medicine,2021,36(04):17.[doi:10.3969/j.issn.1671-7414.2021.06.004]
[7]刘静雅,张海亮,李宝平,等.长链非编码 RNA SNHG1在子宫内膜癌中的表达及调控 PI3K/AKT信号通路的研究[J].现代检验医学杂志,2022,37(01):119.[doi:10.3969/j.issn.1671-7414.2022.01.024]
 LIU Jing-ya,ZHANG Hai-liang,LI Bao-ping,et al.Expression of Long Non-coding RNA SNHG1 in Endometrial Carcinoma and Its Regulation of PI3K/AKT Signaling Pathway[J].Journal of Modern Laboratory Medicine,2022,37(04):119.[doi:10.3969/j.issn.1671-7414.2022.01.024]
[8]彭 浩,张印星,谢 环.长链非编码RNA CDKN2BAS 在子宫内膜癌组织表达及其生物学功能研究[J].现代检验医学杂志,2023,38(03):92.[doi:10.3969/j.issn.1671-7414.2023.03.016]
 PENG Hao,ZHANG Yin-xing,XIE Huan.Expression and Biological Function of Long Non-coding RNA CDKN2BAS in Endometrial Carcinoma[J].Journal of Modern Laboratory Medicine,2023,38(04):92.[doi:10.3969/j.issn.1671-7414.2023.03.016]
[9]梁燕茹,郑 瑜,李 倩.子宫内膜癌患者术前血清apo AI 和Apelin 水平检测对预测淋巴脉管间隙浸润风险的价值研究[J].现代检验医学杂志,2023,38(05):53.[doi:10.3969/j.issn.1671-7414.2023.05.010]
 LIANG Yanru,ZHENG Yu,LI Qian.Value of Preoperative Serum Apo AI and Apelin Levels in Predicting the Risk of Lymph Node Vascular Space Infiltration in Patients with Endometrial Cancer[J].Journal of Modern Laboratory Medicine,2023,38(04):53.[doi:10.3969/j.issn.1671-7414.2023.05.010]
[10]陆 瑞,郭红霞,吴苗苗,等.KIF18B 通过激活Wnt/β catenin 信号通路促进子宫内膜癌细胞增殖和转移的实验研究[J].现代检验医学杂志,2023,38(05):58.[doi:10.3969/j.issn.1671-7414.2023.05.011]
 LU Rui,GUO Hongxia,WU Miaomiao,et al.Experimental Study of KIF18B Promoting Endometrial Cancer Cell Proliferation and Metastasis by Activating Wnt/β-catenin Signaling Pathway[J].Journal of Modern Laboratory Medicine,2023,38(04):58.[doi:10.3969/j.issn.1671-7414.2023.05.011]

备注/Memo

备注/Memo:
基金项目:河北省“三三三人才工程”资助项目(C20221122)。
作者简介:安立娟(1982-),女,硕士研究生,主治医师,研究方向:妇科肿瘤,E-mail:anlijuan820226@163.com。
通讯作者:杨伟伟,男,硕士研究生,主治医师,研究方向:妇科肿瘤,E-mail:1145293016@qq.com。
更新日期/Last Update: 2025-07-15