Tropomodulin 3 Overexpression as a Marker for Platinum Resistance and Immune Infiltration in Ovarian Cancer.

IF 1.2 4区 综合性期刊 Q3 MULTIDISCIPLINARY SCIENCES
Dingwen Xu, Xiaofei Hu, Yang Feng, Zhihua Lu, Xianmei Liu, Huishen Yan, Jianming Peng, Sen Luo, Weijuan Yao
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引用次数: 0

Abstract

The cytoskeleton plays an important role in platinum resistance in ovarian cancer. Tropomodulin 3 (TMOD3) is critical in the development of many tumors, but its role in the drug resistance of ovarian cancer remains unexplored. By analyzing data from the Gene Expression Omnibus (GEO), The Cancer Genome Atlas (TCGA), and Clinical Proteomic Tumor Analysis Consortium (CPTAC) databases, this study compared TMOD3 expression in ovarian cancer and normal tissues, and examined the expression of TMOD3 after platinum treatment in platinum-sensitive and platinum-resistant ovarian cancers. The Kaplan-Meier method was used to assess the effect of TMOD3 on overall survival (OS) and progression-free survival (PFS) in ovarian cancer patients. microRNAs (miRNAs) targeting TMOD3 were predicted using TargetScan and analyzed using the TCGA database. Tumor Immune Estimation Resource (TIMER) and an integrated repository portal for tumor-immune system interactions (TISIDB) were used to determine the relationship between TMOD3 expression and immune infiltration. TMOD3 coexpression networks in ovarian cancer were explored using LinkedOmics, the Search Tool for the Retrieval of Interacting Genes/Proteins (STRING), and The Database for Annotation, Visualization, and Integrated Discovery (DAVID) Bioinformatics. The results showed that TMOD3 was highly expressed in ovarian cancer and was associated with the grading, staging, and metastasis of ovarian cancer. TMOD3 expression was significantly reduced in platinum-treated ovarian cancer cells and patients. However, TMOD3 expression was higher in platinum-resistant ovarian cancer cells and tissues compared to platinum-sensitive ones. Higher TMOD3 expression was significantly associated with lower OS and PFS in ovarian cancer patients treated with platinum-based chemotherapy. miRNA-mediated post-transcriptional regulation is likely responsible for high TMOD3 expression in ovarian cancer and platinum-resistant ovarian tissues. The expression of TMOD3 mRNA was associated with immune infiltration in ovarian cancer. These findings indicate that TMOD3 is highly expressed in ovarian cancer and is closely associated with platinum resistance and immune infiltration.

作为卵巢癌铂类抗性和免疫渗透标志物的托品糖蛋白 3 过度表达
细胞骨架在卵巢癌的铂类耐药性中发挥着重要作用。Tropomodulin 3(TMOD3)在许多肿瘤的发生发展过程中起着关键作用,但它在卵巢癌耐药性中的作用仍有待探索。本研究通过分析基因表达总库(GEO)、癌症基因组图谱(TCGA)和临床蛋白质组肿瘤分析联盟(CPTAC)数据库中的数据,比较了TMOD3在卵巢癌和正常组织中的表达,并研究了铂敏感和铂耐药卵巢癌在铂治疗后TMOD3的表达。该研究采用 Kaplan-Meier 法评估 TMOD3 对卵巢癌患者总生存期(OS)和无进展生存期(PFS)的影响。利用肿瘤免疫估算资源(TIMER)和肿瘤免疫系统相互作用综合资源库门户网站(TISIDB)确定了TMOD3表达与免疫浸润之间的关系。利用LinkedOmics、检索相互作用基因/蛋白的搜索工具(STRING)和注释、可视化和综合发现数据库(DAVID)生物信息学探索了卵巢癌中的TMOD3共表达网络。结果显示,TMOD3在卵巢癌中高表达,并与卵巢癌的分级、分期和转移有关。TMOD3在铂治疗的卵巢癌细胞和患者中的表达明显降低。然而,与对铂类药物敏感的卵巢癌细胞和组织相比,铂类药物耐药的卵巢癌细胞和组织中 TMOD3 的表达更高。在接受铂类化疗的卵巢癌患者中,TMOD3的高表达与较低的OS和PFS显著相关。miRNA介导的转录后调控可能是TMOD3在卵巢癌和铂类耐药卵巢组织中高表达的原因。TMOD3 mRNA的表达与卵巢癌的免疫浸润有关。这些研究结果表明,TMOD3在卵巢癌中高表达,并与铂类耐药性和免疫浸润密切相关。
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来源期刊
Jove-Journal of Visualized Experiments
Jove-Journal of Visualized Experiments MULTIDISCIPLINARY SCIENCES-
CiteScore
2.10
自引率
0.00%
发文量
992
期刊介绍: JoVE, the Journal of Visualized Experiments, is the world''s first peer reviewed scientific video journal. Established in 2006, JoVE is devoted to publishing scientific research in a visual format to help researchers overcome two of the biggest challenges facing the scientific research community today; poor reproducibility and the time and labor intensive nature of learning new experimental techniques.
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