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胰腺癌形态的生物学。

The biology of pancreatic cancer morphology.

机构信息

Department of Pathology and Laboratory Medicine, University of Miami Miller School of Medicine, Miami, FL, USA.

出版信息

Pathology. 2022 Mar;54(2):236-247. doi: 10.1016/j.pathol.2021.09.012. Epub 2021 Dec 3.

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal of all human malignancies. PDAC precursor lesions, invasive primary PDAC, and metastatic PDAC each display distinct morphologies that reflect unique biology. This 'biomorphology' is determined by a complex neoplastic history of clonal phylogenetic relationships, geographic locations, external environmental exposures, intrinsic metabolic demands, and tissue migration patterns. Understanding the biomorphological evolution of PDAC progression is not only of academic interest but also of great practical value. Applying this knowledge to surgical pathology practice facilitates the correct diagnosis on routine H&E stains without additional ancillary studies in most cases. Here I provide a concise overview of the entire biomorphological spectrum of PDAC progression beginning with initial neoplastic transformation and ending in terminal distant metastasis. Most biopsy and resection specimens are currently obtained prior to treatment. As such, our understanding of untreated PDAC biomorphology is mature. The biomorphology of treated PDAC is less defined but will assume greater importance as the frequency of neoadjuvant therapy increases. Although this overview is slanted towards pathology, it is written so that pathologists, clinicians, and scientists alike might find it instructive for their respective disciplines.

摘要

胰腺导管腺癌 (PDAC) 是所有人类恶性肿瘤中最致命的一种。PDAC 的前体病变、侵袭性原发性 PDAC 和转移性 PDAC 各自具有独特的形态,反映了独特的生物学特性。这种“生物形态学”是由克隆系统发育关系、地理位置、外部环境暴露、内在代谢需求和组织迁移模式的复杂肿瘤史决定的。了解 PDAC 进展的生物形态学演变不仅具有学术意义,而且具有重要的实际价值。将这方面的知识应用于外科病理学实践中,可以在大多数情况下,无需额外的辅助研究,仅依靠常规的 H&E 染色即可正确诊断。在这里,我简要概述了 PDAC 进展的整个生物形态谱,从最初的肿瘤转化开始,一直到终末期远处转移结束。目前,大多数活检和切除标本都是在治疗前获得的。因此,我们对未经治疗的 PDAC 生物形态学的理解已经很成熟。治疗后的 PDAC 生物形态学定义较少,但随着新辅助治疗频率的增加,它将变得更加重要。尽管本文主要偏向于病理学,但它的撰写方式使病理学家、临床医生和科学家都可以从各自的学科中得到启发。

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本文引用的文献

1
Intratumor heterogeneity reflects clinical disease course.
Nat Cancer. 2020 Jan;1(1):3-6. doi: 10.1038/s43018-019-0002-1.
2
A unifying paradigm for transcriptional heterogeneity and squamous features in pancreatic ductal adenocarcinoma.
Nat Cancer. 2020 Jan;1(1):59-74. doi: 10.1038/s43018-019-0010-1. Epub 2020 Jan 13.
4
The CD155/TIGIT axis promotes and maintains immune evasion in neoantigen-expressing pancreatic cancer.
Cancer Cell. 2021 Oct 11;39(10):1342-1360.e14. doi: 10.1016/j.ccell.2021.07.007. Epub 2021 Aug 5.
5
Metabolic networks in mutant KRAS-driven tumours: tissue specificities and the microenvironment.
Nat Rev Cancer. 2021 Aug;21(8):510-525. doi: 10.1038/s41568-021-00375-9. Epub 2021 Jul 9.
6
Early detection of pancreatic cancer using DNA-based molecular approaches.
Nat Rev Gastroenterol Hepatol. 2021 Jul;18(7):457-468. doi: 10.1038/s41575-021-00470-0. Epub 2021 Jun 7.
7
The pancreatic cancer genome revisited.
Nat Rev Gastroenterol Hepatol. 2021 Jul;18(7):469-481. doi: 10.1038/s41575-021-00463-z. Epub 2021 Jun 4.
8
Cell of Origin Influences Pancreatic Cancer Subtype.
Cancer Discov. 2021 Mar;11(3):660-677. doi: 10.1158/2159-8290.CD-20-0633.
9
Commitment and oncogene-induced plasticity of human stem cell-derived pancreatic acinar and ductal organoids.
Cell Stem Cell. 2021 Jun 3;28(6):1090-1104.e6. doi: 10.1016/j.stem.2021.03.022. Epub 2021 Apr 28.
10
EPHA2-dependent outcompetition of KRASG12D mutant cells by wild-type neighbors in the adult pancreas.
Curr Biol. 2021 Jun 21;31(12):2550-2560.e5. doi: 10.1016/j.cub.2021.03.094. Epub 2021 Apr 22.

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