Identification of exosome-related SERPINB1 as a novel predictor for tumor immune microenvironment and clinical outcomes in ovarian cancer.

IF 3.8 3区 医学 Q1 REPRODUCTIVE BIOLOGY
Rui Gu, Liping Jiang, Shuqin Dai, Yajie Yue, Shangjin Li, Shudan Zheng, Liwei Wu, Shaojie Zhao
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引用次数: 0

Abstract

Background: With a high global incidence of over three million new cases in 2020 and a high mortality of over two million fatalities, ovarian cancer is one of the most common malignant tumors in gynecology. Exosomes can control the immunological condition of the tumor microenvironment (TME) by participating in intercellular interactions. Therefore, we aimed to construct an exosome-related prognostic model to predict the clinical outcomes of ovarian cancer patients.

Methods: In this research, expression patterns of exosome-related genes were examined in multiple single-cell RNA-sequencing and bulk RNA-sequencing datasets. In addition, a novel exosome-related prognostic model was established by the least absolute shrinkage and selection operator (LASSO) regression method. Then, the correlations between risk score and immunological characteristics of the TME were explored. Moreover, SERPINB1, a gene in the prognostic signature, was further analyzed to reveal its value as a novel biomarker.

Results: In the current study, combined with single-cell and bulk omics datasets, we constructed an exosome-related prognostic model of four genes (LGALS3BP, SAT1, SERPINB1, and SH3BGRL3). Moreover, the risk score was associated with worse overall survival (OS) in ovarian cancer patients. Further analysis found that patients with high-risk score tended to shape a desert TME with hardly infiltration of immune cells. Then, SERPINB1, positively correlated with the favorable OS and negatively with the risk score, was chosen as the representative biomarker of the model. Moreover, SERPINB1 was positively correlated with the infiltration of immune subpopulations in both public and in-house cohort. In addition, the high-resolution analysis found that SERPINB1+ tumor cells communicated with microenvironment cells frequently, further explaining the potential reason for shaping an inflamed TME.

Conclusion: To sum up, we established a novel exosome-related prognostic model (LGALS3BP, SAT1, SERPINB1, and SH3BGRL3) to predict the prognosis of patients with ovarian cancer and identify the immunological characteristics of the TME. In addition, SERPINB1 was identified as a promising biomarker for prognostic prediction in ovarian cancer.

鉴定外泌体相关SERPINB1作为卵巢癌肿瘤免疫微环境和临床结局的新预测因子
背景:卵巢癌是妇科最常见的恶性肿瘤之一,2020年全球新发病例超过300万,死亡率超过200万。外泌体通过参与细胞间相互作用来控制肿瘤微环境(TME)的免疫状态。因此,我们旨在构建外泌体相关的预后模型来预测卵巢癌患者的临床结局。方法:在本研究中,通过多个单细胞rna测序和大量rna测序数据集检测外泌体相关基因的表达模式。此外,采用最小绝对收缩和选择算子(LASSO)回归方法建立了一种新的外泌体相关预后模型。然后,探讨风险评分与TME免疫学特征的相关性。此外,进一步分析了预后标志基因SERPINB1,以揭示其作为新型生物标志物的价值。结果:在目前的研究中,我们结合单细胞和大量组学数据集,构建了四个基因(LGALS3BP、SAT1、SERPINB1和SH3BGRL3)的外泌体相关预后模型。此外,风险评分与卵巢癌患者较差的总生存期(OS)相关。进一步分析发现,高危评分患者倾向于形成沙漠型TME,免疫细胞几乎没有浸润。然后,选择SERPINB1作为模型的代表性生物标志物,SERPINB1与有利OS呈正相关,与风险评分负相关。此外,SERPINB1在公共和内部队列中与免疫亚群的浸润呈正相关。此外,高分辨率分析发现SERPINB1+肿瘤细胞与微环境细胞频繁交流,进一步解释了形成炎症TME的潜在原因。结论:综上所述,我们建立了一种新的外泌体相关预后模型(LGALS3BP、SAT1、SERPINB1、SH3BGRL3)来预测卵巢癌患者的预后,鉴别TME的免疫学特征。此外,SERPINB1被确定为卵巢癌预后预测的有希望的生物标志物。
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来源期刊
Journal of Ovarian Research
Journal of Ovarian Research REPRODUCTIVE BIOLOGY-
CiteScore
6.20
自引率
2.50%
发文量
125
审稿时长
>12 weeks
期刊介绍: Journal of Ovarian Research is an open access, peer reviewed, online journal that aims to provide a forum for high-quality basic and clinical research on ovarian function, abnormalities, and cancer. The journal focuses on research that provides new insights into ovarian functions as well as prevention and treatment of diseases afflicting the organ. Topical areas include, but are not restricted to: Ovary development, hormone secretion and regulation Follicle growth and ovulation Infertility and Polycystic ovarian syndrome Regulation of pituitary and other biological functions by ovarian hormones Ovarian cancer, its prevention, diagnosis and treatment Drug development and screening Role of stem cells in ovary development and function.
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