A platelet-related signature for predicting the prognosis and immunotherapy benefit in bladder cancer based on machine learning combinations.

IF 1.9 3区 医学 Q4 ANDROLOGY Translational andrology and urology Pub Date : 2024-08-31 Epub Date: 2024-08-26 DOI:10.21037/tau-24-80
Cheng Chen, Jun Zhang, Xiaoshuang Liu, Qianfeng Zhuang, Hao Lu, Jianquan Hou
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Abstract

Background: Bladder cancer carries a large societal burden, with over 570,000 newly diagnosed cases and 210,000 deaths globally each year. Platelets play vital functions in tumor progression and therapy benefits. We aimed to construct a platelet-related signature (PRS) for the clinical outcome of bladder cancer cases.

Methods: Ten machine learning techniques were used in the integrative operations to build PRS using the datasets from The Cancer Genome Atlas (TCGA), gene series expression (GSE)13507, GSE31684, GSE32894 and GSE48276. A number of immunotherapy datasets and prediction scores, including GSE91061, GSE78220, and IMvigor210, were utilized to assess how well the PRS predicted the benefit of immunotherapy. Vitro experiment was performed to verify the role of α1C-tubulin (TUBA1C) in bladder cancer.

Results: Enet (alpha =0.4) algorithm-based PRS had the highest average C-index of 0.73 and it was suggested as the optimal PRS. PRS acted as an independent risk factor for bladder cancer and patients with high PRS score portended a worse overall survival rate, with the area under the curve of 1-, 3- and 5-year operating characteristic curve being 0.754, 0.779 and 0.806 in TCGA dataset. A higher level of immune-activated cells, cytolytic function and T cell co-stimulation was found in the low PRS score group. Low PRS score demonstrated a higher tumor mutation burden score and programmed cell death protein 1 & cytotoxic T-lymphocyte associated protein 4 immunophenoscore, lower tumor immune dysfunction and exclusion score, intratumor heterogeneity score and immune escape score in bladder cancer, suggesting the PRS as an indicator for predicting immunotherapy benefits. Vitro experiment showed that TUBA1C was upregulated in bladder cancer and knockdown of TUBA1C obviously suppressed tumor cell proliferation.

Conclusions: The present study developed an ideal PRS for bladder cancer, which may be used as a predictor of prognosis, a risk classification system, and a therapy guide.

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基于机器学习组合的用于预测膀胱癌预后和免疫疗法疗效的血小板相关特征。
背景:膀胱癌给社会带来沉重负担,全球每年有超过 570,000 例新确诊病例和 210,000 例死亡病例。血小板在肿瘤进展和治疗获益方面发挥着重要作用。我们旨在为膀胱癌病例的临床结果构建一个血小板相关特征(PRS):方法:我们使用了十种机器学习技术,利用癌症基因组图谱(TCGA)、基因系列表达(GSE)13507、GSE31684、GSE32894 和 GSE48276 的数据集进行整合操作,以构建 PRS。为了评估PRS预测免疫疗法获益的效果,我们使用了一些免疫疗法数据集和预测分数,包括GSE91061、GSE78220和IMvigor210。体外实验验证了α1C-微管蛋白(TUBA1C)在膀胱癌中的作用:结果:基于 Enet 算法(α =0.4)的 PRS 平均 C 指数最高,为 0.73,被认为是最佳 PRS。PRS是膀胱癌的独立风险因素,PRS得分高的患者总生存率较低,在TCGA数据集中,1年、3年和5年运行特征曲线下面积分别为0.754、0.779和0.806。低 PRS 评分组的免疫激活细胞、细胞溶解功能和 T 细胞协同刺激水平更高。低PRS评分组的肿瘤突变负荷评分、程序性细胞死亡蛋白1和细胞毒性T淋巴细胞相关蛋白4的免疫表观评分较高,肿瘤免疫功能障碍和排斥评分、肿瘤内异质性评分和免疫逃逸评分较低,这表明PRS是预测免疫疗法疗效的一个指标。体外实验表明,TUBA1C在膀胱癌中上调,敲除TUBA1C可明显抑制肿瘤细胞的增殖:本研究为膀胱癌建立了理想的PRS,可作为预后预测指标、风险分类系统和治疗指南。
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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
80
期刊介绍: ranslational Andrology and Urology (Print ISSN 2223-4683; Online ISSN 2223-4691; Transl Androl Urol; TAU) is an open access, peer-reviewed, bi-monthly journal (quarterly published from Mar.2012 - Dec. 2014). The main focus of the journal is to describe new findings in the field of translational research of Andrology and Urology, provides current and practical information on basic research and clinical investigations of Andrology and Urology. Specific areas of interest include, but not limited to, molecular study, pathology, biology and technical advances related to andrology and urology. Topics cover range from evaluation, prevention, diagnosis, therapy, prognosis, rehabilitation and future challenges to urology and andrology. Contributions pertinent to urology and andrology are also included from related fields such as public health, basic sciences, education, sociology, and nursing.
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