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本文引用的文献

1
Genetic analyses of isolated high-grade pancreatic intraepithelial neoplasia (HG-PanIN) reveal paucity of alterations in TP53 and SMAD4.对孤立性高级别胰腺上皮内瘤变(HG-PanIN)的基因分析显示,TP53和SMAD4的改变很少。
J Pathol. 2017 May;242(1):16-23. doi: 10.1002/path.4884. Epub 2017 Mar 30.
2
Pancreatic Ductal Adenocarcinoma and Its Variants.胰腺导管腺癌及其变体
Surg Pathol Clin. 2016 Dec;9(4):547-560. doi: 10.1016/j.path.2016.05.003. Epub 2016 Oct 12.
3
Invasive ductal carcinoma of the breast with osteoclast-like giant cells and clear cell features: a case report of a novel finding and review of the literature.伴有破骨细胞样巨细胞和透明细胞特征的乳腺浸润性导管癌:一例新发现病例报告及文献复习
World J Surg Oncol. 2016 Aug 26;14(1):227. doi: 10.1186/s12957-016-0982-6.
4
Undifferentiated Carcinoma With Osteoclastic Giant Cells of the Pancreas: Clinicopathologic Analysis of 38 Cases Highlights a More Protracted Clinical Course Than Currently Appreciated.胰腺未分化癌伴破骨细胞样巨细胞:38例临床病理分析显示临床病程比目前认识的更迁延。
Am J Surg Pathol. 2016 Sep;40(9):1203-16. doi: 10.1097/PAS.0000000000000689.
5
Targeted DNA Sequencing Reveals Patterns of Local Progression in the Pancreatic Remnant Following Resection of Intraductal Papillary Mucinous Neoplasm (IPMN) of the Pancreas.靶向DNA测序揭示胰腺导管内乳头状黏液性肿瘤(IPMN)切除术后胰腺残余局部进展模式。
Ann Surg. 2017 Jul;266(1):133-141. doi: 10.1097/SLA.0000000000001817.
6
Up-regulation of SERPINA3 correlates with high mortality of melanoma patients and increased migration and invasion of cancer cells.丝氨酸蛋白酶抑制剂A3(SERPINA3)的上调与黑色素瘤患者的高死亡率以及癌细胞迁移和侵袭增加相关。
Oncotarget. 2017 Mar 21;8(12):18712-18725. doi: 10.18632/oncotarget.9409.
7
A case of pulmonary adenocarcinoma harboring osteoclast-like giant cells: Its evaluation by immunohistochemical and genetic analyses.一例伴有破骨细胞样巨细胞的肺腺癌:通过免疫组织化学和基因分析进行评估
Pathol Int. 2016 Apr;66(4):224-9. doi: 10.1111/pin.12395. Epub 2016 Mar 3.
8
Genomic analyses identify molecular subtypes of pancreatic cancer.基因组分析确定了胰腺癌的分子亚型。
Nature. 2016 Mar 3;531(7592):47-52. doi: 10.1038/nature16965. Epub 2016 Feb 24.
9
Reporting tumor molecular heterogeneity in histopathological diagnosis.在组织病理学诊断中报告肿瘤分子异质性。
PLoS One. 2014 Aug 15;9(8):e104979. doi: 10.1371/journal.pone.0104979. eCollection 2014.
10
The UPF1 RNA surveillance gene is commonly mutated in pancreatic adenosquamous carcinoma.UPF1 RNA 监测基因在胰腺腺鳞癌中常发生突变。
Nat Med. 2014 Jun;20(6):596-8. doi: 10.1038/nm.3548. Epub 2014 May 25.

伴有破骨细胞样巨细胞的胰腺未分化癌在基因上与传统导管腺癌相似,但在临床上有所不同。

Pancreatic undifferentiated carcinoma with osteoclast-like giant cells is genetically similar to, but clinically distinct from, conventional ductal adenocarcinoma.

作者信息

Luchini Claudio, Pea Antonio, Lionheart Gemma, Mafficini Andrea, Nottegar Alessia, Veronese Nicola, Chianchiano Peter, Brosens Lodewijk Aa, Noë Michaël, Offerhaus G Johan A, Yonescu Raluca, Ning Yi, Malleo Giuseppe, Riva Giulio, Piccoli Paola, Cataldo Ivana, Capelli Paola, Zamboni Giuseppe, Scarpa Aldo, Wood Laura D

机构信息

Department of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.

Department of Pathology, Sol Goldman Pancreatic Cancer Research Center, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

J Pathol. 2017 Oct;243(2):148-154. doi: 10.1002/path.4941. Epub 2017 Sep 5.

DOI:10.1002/path.4941
PMID:28722124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6664430/
Abstract

Undifferentiated carcinoma of the pancreas with osteoclast-like giant cells (UCOGC) is currently considered a morphologically and clinically distinct variant of pancreatic ductal adenocarcinoma (PDAC). In this study, we report clinical and pathological features of a series of 22 UCOGCs, including the whole exome sequencing of eight UCOGCs. We observed that 60% of the UCOGCs contained a well-defined epithelial component and that patients with pure UCOGC had a significantly better prognosis than did those with an UCOGC with an associated epithelial neoplasm. The genetic alterations in UCOGC are strikingly similar to those known to drive conventional PDAC, including activating mutations in the oncogene KRAS and inactivating mutations in the tumor suppressor genes CDKN2A, TP53, and SMAD4. These results further support the classification of UCOGC as a PDAC variant and suggest that somatic mutations are not the determinants of the unique phenotype of UCOGC. Copyright © 2017 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

摘要

伴有破骨细胞样巨细胞的胰腺未分化癌(UCOGC)目前被认为是胰腺导管腺癌(PDAC)在形态学和临床上的一种独特变体。在本研究中,我们报告了一系列22例UCOGC的临床和病理特征,包括8例UCOGC的全外显子组测序。我们观察到60%的UCOGC含有明确的上皮成分,并且纯UCOGC患者的预后明显优于伴有相关上皮性肿瘤的UCOGC患者。UCOGC中的基因改变与已知驱动传统PDAC的改变惊人地相似,包括癌基因KRAS的激活突变以及肿瘤抑制基因CDKN2A、TP53和SMAD4的失活突变。这些结果进一步支持将UCOGC归类为PDAC变体,并表明体细胞突变不是UCOGC独特表型的决定因素。版权所有© 2017英国及爱尔兰病理学会。由约翰·威利父子有限公司出版。