Yujie Xiao, Manal Elmasry, Ji Dong K. Bai, Andrew Chen, Yuzhu Chen, Brooke Jackson, Joseph O. Johnson, Prateek Prasanna, Chao Chen, Mehdi Damaghi
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Quantitative analyses were performed on immuno-histological images from a retrospective cohort of DCIS specimens collected from biopsy samples. First, an eco-evolutionary designed approach was developed to define habitats in the tumor intra-ductal microenvironment based on oxygen diffusion distance. Then, cancer cells with metabolic phenotypes attributed to their habitats were identified, including a hypoxia-responding CA9+ phenotype and an acid-adapted LAMP2b+ phenotype. While these markers have traditionally shown limited, if any, predictive capabilities for DCIS progression, when analyzed from an ecological perspective, their power to differentiate between non-upstaged and upstaged DCIS increased significantly. Additionally, the distribution of distinct niches with specific spatial patterns of these biomarkers predicted patient upstaging. The niches were characterized by pattern analysis of both cellular and spatial features. 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引用次数: 0
摘要
癌症在一个动态的生态系统中进化。因此,描述癌症的生态动态对于理解癌症进化至关重要,这可以导致发现预测疾病进展的生物标志物。导管原位癌(Ductal carcinoma in situ, DCIS)是一种以乳管内异常上皮细胞生长为特征的早期乳腺癌,需要生物标志物来预测哪些病例会发展为侵袭性疾病。在这项研究中,我们发现缺氧和酸中毒生物标志物的生态学分析可以显著提高对DCIS的预测。定量分析了从活检样本中收集的DCIS标本的回顾性队列的免疫组织学图像。首先,建立了一种基于氧扩散距离的肿瘤导管内微环境的生态进化设计方法。然后,鉴定出具有归因于其栖息地的代谢表型的癌细胞,包括缺氧反应CA9+表型和酸适应LAMP2b+表型。虽然传统上这些标志物对DCIS进展的预测能力有限(如果有的话),但从生态学的角度分析,它们区分非隐性DCIS和隐性DCIS的能力显著增强。此外,具有这些生物标志物特定空间模式的不同生态位的分布预测了患者的抢先期。对生态位进行了细胞特征和空间特征的模式分析。随机森林分类器经过训练并在活检队列中进行了5倍验证,预测临床结果的曲线下面积(AUC)为0.74。这些结果肯定了肿瘤生态特征在生态进化设计的生物标志物发现方法中的重要性。
Eco-evolutionary Guided Pathomic Analysis Detects Biomarkers to Predict Ductal Carcinoma In Situ Upstaging
Cancers evolve in a dynamic ecosystem. Thus, characterizing the ecological dynamics of cancer is crucial to understanding cancer evolution, which can lead to the discovery of biomarkers to predict disease progression. Ductal carcinoma in situ (DCIS) is an early-stage breast cancer characterized by abnormal epithelial cell growth confined within the milk ducts, and biomarkers are needed to predict which cases will progress to aggressive disease. In this study, we showed that ecological analysis of hypoxia and acidosis biomarkers can significantly improve prediction of DCIS upstaging. Quantitative analyses were performed on immuno-histological images from a retrospective cohort of DCIS specimens collected from biopsy samples. First, an eco-evolutionary designed approach was developed to define habitats in the tumor intra-ductal microenvironment based on oxygen diffusion distance. Then, cancer cells with metabolic phenotypes attributed to their habitats were identified, including a hypoxia-responding CA9+ phenotype and an acid-adapted LAMP2b+ phenotype. While these markers have traditionally shown limited, if any, predictive capabilities for DCIS progression, when analyzed from an ecological perspective, their power to differentiate between non-upstaged and upstaged DCIS increased significantly. Additionally, the distribution of distinct niches with specific spatial patterns of these biomarkers predicted patient upstaging. The niches were characterized by pattern analysis of both cellular and spatial features. A random forest classifier that was trained and underwent a 5-fold validation on the biopsy cohort achieved an area under curve (AUC) of 0.74 for predicting clinical outcome. These results affirm the importance of tumor ecological features in eco-evolutionary-designed approaches for biomarker discovery.
期刊介绍:
Cancer Research, published by the American Association for Cancer Research (AACR), is a journal that focuses on impactful original studies, reviews, and opinion pieces relevant to the broad cancer research community. Manuscripts that present conceptual or technological advances leading to insights into cancer biology are particularly sought after. The journal also places emphasis on convergence science, which involves bridging multiple distinct areas of cancer research.
With primary subsections including Cancer Biology, Cancer Immunology, Cancer Metabolism and Molecular Mechanisms, Translational Cancer Biology, Cancer Landscapes, and Convergence Science, Cancer Research has a comprehensive scope. It is published twice a month and has one volume per year, with a print ISSN of 0008-5472 and an online ISSN of 1538-7445.
Cancer Research is abstracted and/or indexed in various databases and platforms, including BIOSIS Previews (R) Database, MEDLINE, Current Contents/Life Sciences, Current Contents/Clinical Medicine, Science Citation Index, Scopus, and Web of Science.