Cell Type of Pancreatic Ductal Adenocarcinoma Origin: Implications for Prognosis and Clinical Outcomes.

IF 1.8 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Shilpa Patil, Yan Dou, Janel L Kopp
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引用次数: 2

Abstract

Background: Pancreatic ductal adenocarcinoma (PDAC) is a devastating disease that has no effective early detection method or treatment to date.

Summary: The normal cell type that initiates PDAC, or its cellular origin, is still unknown. To investigate the contribution of distinct normal epithelial cell types to PDAC tumorigenesis, genetically engineered mouse models were used to show that both acinar and ductal cells are capable of giving rise to PDAC. These studies indicated that genetic mutations and pancreatic injury interact differently with each cellular origin to affect their predilection and process for forming PDAC. In this review, we summarize recent findings using various genetically engineered mouse models in the identification and characterization of the PDAC cell of origin. We also discuss potential implications for cellular origin on tumor development, PDAC transcriptional subtype, and disease prognosis of patients.

Key message: Although it is clear that both ductal and acinar cells have the potential to form PDAC, whether cellular origin can indeed influence patient prognosis and whether knowledge of cellular origin will aid in the diagnosis or treatment of patients in the future will need further study.

胰腺导管腺癌起源的细胞类型:对预后和临床结果的影响。
背景:胰腺导管腺癌(Pancreatic ductal adencarcinoma, PDAC)是一种破坏性疾病,迄今为止尚无有效的早期检测方法或治疗方法。摘要:启动PDAC的正常细胞类型或其细胞起源尚不清楚。为了研究不同的正常上皮细胞类型对PDAC肿瘤发生的贡献,基因工程小鼠模型显示腺泡细胞和导管细胞都能够产生PDAC。这些研究表明,基因突变和胰腺损伤与每个细胞起源的相互作用不同,影响它们的偏好和形成PDAC的过程。在这篇综述中,我们总结了利用各种基因工程小鼠模型在鉴定和表征PDAC细胞来源方面的最新发现。我们还讨论了细胞起源对肿瘤发展、PDAC转录亚型和患者疾病预后的潜在影响。关键信息:虽然导管细胞和腺泡细胞都有形成PDAC的潜力,但细胞起源是否真的会影响患者预后,以及了解细胞起源是否有助于未来患者的诊断或治疗,还需要进一步研究。
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
Visceral Medicine
Visceral Medicine Medicine-Surgery
CiteScore
4.50
自引率
0.00%
发文量
40
期刊介绍: This interdisciplinary journal is unique in its field as it covers the principles of both gastrointestinal medicine and surgery required for treating abdominal diseases. In each issue invited reviews provide a comprehensive overview of one selected topic. Thus, a sound background of the state of the art in clinical practice and research is provided. A panel of specialists in gastroenterology, surgery, radiology, and pathology discusses different approaches to diagnosis and treatment of the topic covered in the respective issue. Original articles, case reports, and commentaries make for further interesting reading.
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