The origin of patient-derived cancer organoids from pathologically undiagnosed specimen in patients with pancreatobiliary cancers.

IF 6.6 2区 医学 Q1 Medicine
Bomi Kim, Jiho Park, Hee Young Na, Sinwoo Park, Jeonghwa Jin, Kwangrok Jung, Jong-Chan Lee, Jin-Hyeok Hwang, Minseok Seo, Jaihwan Kim
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引用次数: 0

Abstract

Purpose: Tissue confirmation of pancreatobiliary cancer is often difficult because of the location of the tumor and structure of the surrounding blood vessels. Patient-derived cancer organoids (PDCOs) reflect the genomic characteristics of individual cancers. Although diverse attempts to construct PDCOs for various pancreatobiliary cancer models are ongoing, no research results have yet confirmed the possibility of performing a precise diagnosis on PDCOs derived from pathologically negative patient samples.

Methods: We obtained a total of nine samples, including pathologically negative samples, from four patients (three patients with pancreatic cancer and one patient with gallbladder cancer) using different tissue acquisition methods to establish PDCOs (success rate 75%).

Results: We successfully verified whether the constructed PDCOs could represent the tissues of patients with pancreatobiliary cancer at each multi-omics level using tumor panel sequencing, single-cell RNA sequencing, hematoxylin and eosin, and immunohistochemical staining. PDCOs from pathologically negative samples showed expression patterns of malignant ductal cell-related biomarkers similar to those of other pathologically positive samples. Furthermore, the expression patterns at the single-cell level in PDCO from patients ultimately diagnosed with gallbladder cancer after surgery were different from those in patients with pancreatic cancer.

Conclusion: Therefore, our study implicated the potential of PDCOs as diagnostic and research tools, including for case involving limited tissue samples. Based on these results, we anticipate that this could be extended to more advanced studies, such as drug sensitivity testing, through large-scale trials in the near future.

从胰胆管癌患者病理未确诊标本中提取患者衍生癌症器官组织的起源。
目的:胰胆管癌的组织确定由于肿瘤的位置和周围血管的结构,往往是困难的。患者衍生的癌症类器官(PDCOs)反映了个体癌症的基因组特征。尽管各种胰胆癌模型构建PDCOs的尝试正在进行中,但尚未有研究结果证实对来自病理阴性患者样本的PDCOs进行精确诊断的可能性。方法:采用不同的组织获取方法建立PDCOs(成功率75%),共获得4例患者(3例胰腺癌和1例胆囊癌)9例标本,包括病理阴性标本。结果:通过肿瘤面板测序、单细胞RNA测序、苏木精和伊红染色、免疫组化染色,成功验证了构建的PDCOs能否在各个多组学水平上代表胰胆癌患者的组织。病理阴性样本的PDCOs表现出与其他病理阳性样本相似的恶性导管细胞相关生物标志物的表达模式。此外,最终诊断为胆囊癌的患者术后PDCO在单细胞水平上的表达模式与胰腺癌患者不同。结论:因此,我们的研究暗示了PDCOs作为诊断和研究工具的潜力,包括涉及有限组织样本的病例。基于这些结果,我们预计在不久的将来,可以通过大规模试验将其扩展到更高级的研究中,例如药物敏感性测试。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cellular Oncology
Cellular Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
10.40
自引率
1.50%
发文量
0
审稿时长
16 weeks
期刊介绍: The Official Journal of the International Society for Cellular Oncology Focuses on translational research Addresses the conversion of cell biology to clinical applications Cellular Oncology publishes scientific contributions from various biomedical and clinical disciplines involved in basic and translational cancer research on the cell and tissue level, technical and bioinformatics developments in this area, and clinical applications. This includes a variety of fields like genome technology, micro-arrays and other high-throughput techniques, genomic instability, SNP, DNA methylation, signaling pathways, DNA organization, (sub)microscopic imaging, proteomics, bioinformatics, functional effects of genomics, drug design and development, molecular diagnostics and targeted cancer therapies, genotype-phenotype interactions. A major goal is to translate the latest developments in these fields from the research laboratory into routine patient management. To this end Cellular Oncology forms a platform of scientific information exchange between molecular biologists and geneticists, technical developers, pathologists, (medical) oncologists and other clinicians involved in the management of cancer patients. In vitro studies are preferentially supported by validations in tumor tissue with clinicopathological associations.
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