武汉大学中南医院检验科 湖北 武汉 430071
张钰,女,1995—,医学硕士生,主要从事胃癌、肝癌标志物及其分子机制研究,E‑mail:chrisss1226@whu.edu.cn
刘凤莲,女,2001—,医学硕士生,主要从事胃癌标志物及其分子机制研究,E⁃mail:LFL017@whu.edu.cn
涂建成,男,1962—,医学博士,教授,主要从事肝细胞癌发生发展的分子机制研究,E‑mail:jianchengtu@whu.edu.cn
收稿:2024-12-25,
纸质出版:2025-12-25
移动端阅览
张钰,刘凤莲,涂建成.Homer2在胃癌中的诊断价值及功能研究[J].武汉大学学报(医学版),2025,46(12):1559-1571.
ZHANG Yu,LIU Fenglian,TU Jiancheng.Diagnostic and functional value of Homer2 in gastric cancer[J].Medical Journal of Wuhan University,2025,46(12):1559-1571.
张钰,刘凤莲,涂建成.Homer2在胃癌中的诊断价值及功能研究[J].武汉大学学报(医学版),2025,46(12):1559-1571. DOI: 10.14188/j.1671-8852.2024.1019.
ZHANG Yu,LIU Fenglian,TU Jiancheng.Diagnostic and functional value of Homer2 in gastric cancer[J].Medical Journal of Wuhan University,2025,46(12):1559-1571. DOI: 10.14188/j.1671-8852.2024.1019.
目的
2
分析Homer2基因在胃癌(GC)中的表达水平,评估其在GC中的诊断和预后价值,探究其在GC发生发展中的作用,并分析其与GC肿瘤免疫浸润水平的相关性,预测其是否可作为GC的免疫治疗靶点。
方法
2
(1)通过癌症基因组图谱(TCGA)和人类蛋白质图谱(HPA)数据库获取Homer2在GC中的表达数据;(2)结合临床信息探究Homer2表达水平与临床特征相关性,采用受试者工作特征(ROC)曲线评估其诊断价值;(3)通过GO和KEGG功能富集分析预测Homer2的潜在功能;(4)通过CellMarker和TISIDB数据库分析Homer2与GC肿瘤免疫浸润水平相关性;(4)收集GC患者外周血及临床组织样本,检测Homer2的mRNA表达水平对生物信息学分析结果加以验证;(5)检测常见GC细胞系中Homer2的mRNA和蛋白质表达水平并进行细胞功能学实验;(6)通过OE‑Homer2慢病毒感染NCI‑N87和AGS细胞过表达Homer2,通过CCK‑8细胞增殖实验、克隆形成实验、细胞划痕实验和Transwell侵袭实验观察NCI‑N87和AGS细胞的增殖、迁移和侵袭能力的变化。
结果
2
(1)Homer2在GC组织中表达下调,其表达水平与病理分期、组织学分级、原发肿瘤大小分期和淋巴结转移分期水平呈负相关;(2)基于Homer2表达水平的ROC曲线的曲线下面积(
AUC
)为0.76(95%
CI
:0.691~0.829);(3)Homer2参与Wnt信号通路、参与单原子离子通道络合物且能影响DNA结合转录因子活性及RNA聚合酶Ⅱ的特异性,且与肌动蛋白细胞骨架的调节、MAPK、钙离子、Wnt以及mTOR信号通路的调节有相关性;(4)Homer2表达水平与GC肿瘤免疫浸润水平有一定相关性;(5)Homer2在GC患者外周血及组织中低表达,过表达Homer2后NCI‑N87和AGS细胞系的体外增殖、迁移和侵袭能力降低。以上结果差异均有统计学意义(
P
<
0.05)。
结论
2
Homer2在GC中表达下调;Homer2低表达与GC不良预后相关;Homer2可作为GC的诊断标志物和潜在的免疫治疗靶点。
Objective
2
o analyze the expression level of the Homer2 gene in gastric cancer (GC)
to evaluate its diagnostic and prognostic value
to explore its role in GC development
to analyze its correlation with tumor immune⁃infiltration levels
and to assess its potential as an immunotherapy target for GC.
Methods
2
Homer2 expression data in GC were obtained from The Cancer Genome Atlas (TCGA) and Human Protein Atlas (HPA) databases
and clinical information was combined to investigate the correlation between Homer2 expression levels and clinical characteristics. The diagnostic value of Homer2 was evaluated using the receiver operating characteristic (ROC) curve. The function of Homer2 was predicted through GO and KEGG functional enrichment analysis. The correlation between Homer2 and tumor immune infiltration level was evaluated using CellMarker 2.0
an integrated repository portal for tumor‑immune system interactions (TISIDB) databases. Peripheral blood samples and tumor and non‑tumor samples of GC patients were collected to detect the mRNA expression level of Homer2. Moreover
the mRNA and protein expression levels of Homer2 were detected in common GC cell lines. Homer2 expression was reduced in GC cells via lentivirus infection. Cellular assays
including CCK⁃8 proliferation
clone formation
cell scratch
and Transwell invasion assays
were conducted to observe changes in cell proliferation
migration
and invasion abilities.
Results
2
The bioinformatics analysis showed that Homer2 expression was downregulated in GC tissues and negatively correlated with pathological staging
histological grading
primary tumor size
and lymph node metastasis. The
AUC
value of the ROC curve was 0.76 (95%
CI
: 0.691⁃0.829). Homer2 was involved in the Wnt signaling pathway and ion channel complexes. It can also affect the activity of DNA⁃binding transcription factors and RNA polymerase Ⅱ. Furthermore
Homer2 was related to the regulation of the actin cytoskeleton
MAPK
calcium ion
Wnt
and mTOR signaling pathways. The expression level of Homer2 was correlated with the immune infiltration level in GC tumors. Homer2 was found to be downregulated in the perip
heral blood and tissue samples of patients with GC. Overexpression of Homer2 reduced the
in vitro
proliferation
migration
and invasion of GC cells (
P
<
0.05).
Conclusion
2
The expression of Homer2 was downregulated in GC
and low expression of Homer2 was associated with poor prognosis. Homer2 can be used as a diagnostic marker and a potential target for immunotherapy in GC.
International Agency for Research on Cancer , World Health Organization . CI 5 Ⅻ: Cancer incidence in five continents volumeⅫ[EB/OL ] . [ 2024‑10‑02 ] . https://ci5.iarc.who.int/ https://ci5.iarc.who.int/ .
BRAY F , LAVERSANNE M , SUNG H , et al . Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries [J ] . CA Cancer J Clin , 2024 , 74 ( 3 ): 229 ‑ 263 .
SALONI W , KATE L , ROXANNE M , et al . The role of homer scaffolding protein 2 (Homer2) in endometrial cancer [J ] . Modern Pathology , 2017 , 30 : 314A .
LUO P , LIANG C , JING W , et al . Homer2 and Homer3 act as novel biomarkers in diagnosis of hepatitis B virus‑induced hepatocellular carcinoma [J ] . J Cancer , 2021 , 12 ( 12 ): 3439 ‑ 3447 .
MHAWECH‑FAUCEGLIA P , WALIA S , YESSAIAN A , et al . Overexpression of HOMER2 predicts better outcome in low‑grade endometrioid endometrial adenocarcinoma [J ] . Pathology , 2018 , 50 ( 5 ): 499 ‑ 503 .
KANG J Y , SONG S H , YUN J , et al . Identification of long‑range epigenetic silencing on chromosome 15q25 and its clinical implication in gastric cancer [J ] . Am J Pathol , 2015 , 185 ( 3 ): 666 ‑ 678 .
DART A . Intercepting gastric cancer [J ] . Nat Rev Cancer , 2024 , 24 ( 10 ): 651 .
BASS A J , THORSSON V , SHMULEVICH I , et al . Comprehensive molecular characterization of gastric adenocarcinoma [J ] . Nature , 2014 , 513 : 202 ‑ 209 .
ZHU M , LIANG Q , CHEN T , et al . Identification and validation of methylated differentially expressed miRNAs and immune infiltrate profile in EBV‑associated gastric cancer [J ] . Clin Epigenetics , 2021 , 13 ( 1 ): 22 .
YANG M , LU Z , YU B , et al . COL5A1 promotes the progression of gastric cancer by acting as a CeRNA of miR‑137‑3p to upregulate FSTL1 expression [J ] . Cancers (Basel) , 2022 , 14 ( 13 ): 3244 .
DE VRIES A C , VAN GRIEKEN N C T , LOOMAN C W N , et al . Gastric cancer risk in patients with premalignant gastric lesions: A nationwide cohort study in the Netherlands [J ] . Gastroenterology , 2008 , 134 ( 4 ): 945 ‑ 952 .
FORD A C , FORMAN D , HUNT R , et al . Helicobacter pylori eradication for the prevention of gastric neoplasia [J ] . Cochrane Database Syst Rev , 2015 ( 7 ): CD005583 .
ZHANG Y , WU X , ZHANG C , et al . Dissecting expression profiles of gastric precancerous lesions and early gastric cancer to explore crucial molecules in intestinal‑type gastric cancer tumorigenesis [J ] . J Pathol , 2020 , 251 ( 2 ): 135 ‑ 146 .
ZHANG P , YANG M , ZHANG Y , et al . Dissecting the single‑cell transcriptome network underlying gastric premalignant lesions and early gastric cancer [J ] . Cell Rep , 2019 , 27 ( 6 ): 1934 ‑ 1947.e5 .
ZHANG X , WANG L , LI Z. , et al . Homer family proteins: Structure, function and their role in cancer [J ] . Oncotarget , 2017 , 8 ( 25 ): 4 1893‑ 41903 .
NIEHRS C . The complex world of WNT receptor signalling [J ] . Nat Rev Mol Cell Biol , 2012 , 13 : 767 ‑ 779 .
DHILLON A S , HAGAN S , RATH O , et al . MAP kinase signalling pathways in cancer [J ] . Oncogene , 2007 , 26 ( 22 ): 3279 ‑ 3290 .
刘涛 , 张霞 , 刘登科 , 等 . 胃康宁治疗幽门螺杆菌相关性胃癌前病变临床疗效及对胃黏膜Ki‑67蛋白表达的影响 [J ] . 中国临床医生杂志 , 2017 , 45 ( 6 ): 21 ‑ 24 .
LIU T , ZHANG X , LIU D K , et al . Effect the treatment of Weikangning decoction to HP with gastric precancerous lesions and its influence on Ki‑67 protein expression [J ] . Chin J Clin , 2017 , 45 ( 6 ): 21 ‑ 24 .
杨洋 . 慢性萎缩性胃炎模型大鼠定量蛋白组学及中药干预靶点研究 [D ] . 北京 : 中国中医科学院 , 2017 .
YANG Y . Study on quantitative proteomics of chronic atrophic gastritis model rats and intervention targets of traditional Chinese medicine [D ] . Beijing : China Academy of Chinese Medical Sciences , 2017 .
FRIDMAN W H , PAGÈS F , SAUTÈS‑FRIDMAN C , et al . The immune contexture in human tumours: Impact on clinical outcome [J ] . Nat Rev Cancer , 2012 , 12 : 298 ‑ 306 .
FUCHS C S , DOI T , JANG R W , et al . Safety and efficacy of pembrolizumab monotherapy in patients with previously treated advanced gastric and gastroesophageal junction cancer: Phase 2 clinical KEYNOTE‑059 trial [J ] . JAMA Oncol , 2018 , 4 ( 5 ): e180013 .
0
浏览量
12
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010802024621