Identification of Prognostic Biomarkers for Breast Cancer Metastasis Using Penalized Additive Hazards Regression Model.

IF 2.4 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY Cancer Informatics Pub Date : 2023-01-01 DOI:10.1177/11769351231157942
Leili Tapak, Omid Hamidi, Payam Amini, Saeid Afshar, Siamak Salimy, Irina Dinu
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Abstract

Background: Breast cancer (BC) has been reported as one of the most common cancers diagnosed in females throughout the world. Survival rate of BC patients is affected by metastasis. So, exploring its underlying mechanisms and identifying related biomarkers to monitor BC relapse/recurrence using new statistical methods is essential. This study investigated the high-dimensional gene-expression profiles of BC patients using penalized additive hazards regression models.

Methods: A publicly available dataset related to the time to metastasis in BC patients (GSE2034) was used. There was information of 22 283 genes expression profiles related to 286 BC patients. Penalized additive hazards regression models with different penalties, including LASSO, SCAD, SICA, MCP and Elastic net were used to identify metastasis related genes.

Results: Five regression models with penalties were applied in the additive hazards model and jointly found 9 genes including SNU13, CLINT1, MAPK9, ABCC5, NKX3-1, NCOR2, COL2A1, and ZNF219. According the median of the prognostic index calculated using the regression coefficients of the penalized additive hazards model, the patients were labeled as high/low risk groups. A significant difference was detected in the survival curves of the identified groups. The selected genes were examined using validation data and were significantly associated with the hazard of metastasis.

Conclusion: This study showed that MAPK9, NKX3-1, NCOR1, ABCC5, and CD44 are the potential recurrence and metastatic predictors in breast cancer and can be taken into account as candidates for further research in tumorigenesis, invasion, metastasis, and epithelial-mesenchymal transition of breast cancer.

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使用惩罚加性风险回归模型识别乳腺癌转移的预后生物标志物。
背景:乳腺癌(BC)已被报道为全世界女性最常见的癌症之一。BC患者的生存率受转移的影响。因此,探索其潜在机制和识别相关生物标志物,利用新的统计方法监测BC复发/复发是必要的。本研究使用惩罚加性风险回归模型研究了BC患者的高维基因表达谱。方法:使用与BC患者转移时间相关的公开数据集(GSE2034)。286例BC患者共获得22 283个基因表达谱信息。采用LASSO、SCAD、SICA、MCP和Elastic net等惩罚性加性风险回归模型识别转移相关基因。结果:在加性危害模型中应用了5个带惩罚的回归模型,共发现了SNU13、CLINT1、MAPK9、ABCC5、NKX3-1、NCOR2、COL2A1、ZNF219等9个基因。根据惩罚加性危险模型回归系数计算的预后指数中位数,将患者标记为高/低风险组。鉴定组的生存曲线有显著差异。选择的基因使用验证数据进行检查,并与转移的危险显著相关。结论:本研究显示MAPK9、NKX3-1、NCOR1、ABCC5和CD44是乳腺癌复发和转移的潜在预测因子,可作为进一步研究乳腺癌发生、侵袭、转移和上皮间质转移的候选因子。
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来源期刊
Cancer Informatics
Cancer Informatics Medicine-Oncology
CiteScore
3.00
自引率
5.00%
发文量
30
审稿时长
8 weeks
期刊介绍: The field of cancer research relies on advances in many other disciplines, including omics technology, mass spectrometry, radio imaging, computer science, and biostatistics. Cancer Informatics provides open access to peer-reviewed high-quality manuscripts reporting bioinformatics analysis of molecular genetics and/or clinical data pertaining to cancer, emphasizing the use of machine learning, artificial intelligence, statistical algorithms, advanced imaging techniques, data visualization, and high-throughput technologies. As the leading journal dedicated exclusively to the report of the use of computational methods in cancer research and practice, Cancer Informatics leverages methodological improvements in systems biology, genomics, proteomics, metabolomics, and molecular biochemistry into the fields of cancer detection, treatment, classification, risk-prediction, prevention, outcome, and modeling.
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