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本文引用的文献

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GATA6 Expression Distinguishes Classical and Basal-like Subtypes in Advanced Pancreatic Cancer.GATA6 表达可区分晚期胰腺癌中的经典型和基底样亚型。
Clin Cancer Res. 2020 Sep 15;26(18):4901-4910. doi: 10.1158/1078-0432.CCR-19-3724. Epub 2020 Mar 10.
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Different shades of pancreatic ductal adenocarcinoma, different paths towards precision therapeutic applications.不同程度的胰腺导管腺癌,通向精准治疗应用的不同道路。
Ann Oncol. 2019 Sep 1;30(9):1428-1436. doi: 10.1093/annonc/mdz181.
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Automated Identification and Quantification of Signals in Multichannel Immunofluorescence Images: The SignalFinder-IF Platform.多通道免疫荧光图像中信号的自动识别和定量:SignalFinder-IF 平台。
Am J Pathol. 2019 Jul;189(7):1402-1412. doi: 10.1016/j.ajpath.2019.03.011. Epub 2019 Apr 23.
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Molecular subtypes of pancreatic cancer.胰腺癌的分子亚型。
Nat Rev Gastroenterol Hepatol. 2019 Apr;16(4):207-220. doi: 10.1038/s41575-019-0109-y.
5
The sTRA Plasma Biomarker: Blinded Validation of Improved Accuracy Over CA19-9 in Pancreatic Cancer Diagnosis.sTRA 血浆生物标志物:在胰腺癌诊断中优于 CA19-9 的准确性的盲法验证。
Clin Cancer Res. 2019 May 1;25(9):2745-2754. doi: 10.1158/1078-0432.CCR-18-3310. Epub 2019 Jan 7.
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FOLFIRINOX or Gemcitabine as Adjuvant Therapy for Pancreatic Cancer.FOLFIRINOX 或吉西他滨作为胰腺癌的辅助治疗。
N Engl J Med. 2018 Dec 20;379(25):2395-2406. doi: 10.1056/NEJMoa1809775.
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Importance of Normalization of CA19-9 Levels Following Neoadjuvant Therapy in Patients With Localized Pancreatic Cancer.局部胰腺癌患者新辅助治疗后 CA19-9 水平正常化的重要性。
Ann Surg. 2020 Apr;271(4):740-747. doi: 10.1097/SLA.0000000000003049.
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Prognostic factors for actual long-term survival in the era of multidisciplinary treatment for pancreatic ductal adenocarcinoma.胰腺导管腺癌多学科治疗时代实际长期生存的预后因素。
Langenbecks Arch Surg. 2018 Sep;403(6):693-700. doi: 10.1007/s00423-018-1709-7. Epub 2018 Sep 15.
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Organoid Profiling Identifies Common Responders to Chemotherapy in Pancreatic Cancer.类器官分析鉴定胰腺癌化疗的常见应答者。
Cancer Discov. 2018 Sep;8(9):1112-1129. doi: 10.1158/2159-8290.CD-18-0349. Epub 2018 May 31.
10
Therapeutic developments in pancreatic cancer: current and future perspectives.胰腺癌的治疗进展:现状与未来展望。
Nat Rev Gastroenterol Hepatol. 2018 Jun;15(6):333-348. doi: 10.1038/s41575-018-0005-x.

使用聚糖生物标志物 sTRA 检测化疗耐药性胰腺癌

Detection of Chemotherapy-resistant Pancreatic Cancer Using a Glycan Biomarker, sTRA.

机构信息

Center for Cancer and Cell Biology, Van Andel Institute, Grand Rapids, Michigan.

Lustgarten Foundation Pancreatic Cancer Research Laboratory, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York.

出版信息

Clin Cancer Res. 2021 Jan 1;27(1):226-236. doi: 10.1158/1078-0432.CCR-20-2475. Epub 2020 Oct 22.

DOI:10.1158/1078-0432.CCR-20-2475
PMID:33093149
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7785673/
Abstract

PURPOSE

A subset of pancreatic ductal adenocarcinomas (PDACs) is highly resistant to systemic chemotherapy, but no markers are available in clinical settings to identify this subset. We hypothesized that a glycan biomarker for PDACs called sialylated tumor-related antigen (sTRA) could be used for this purpose.

EXPERIMENTAL DESIGN

We tested for differences between PDACs classified by glycan expression in multiple systems: sets of cell lines, organoids, and isogenic cell lines; primary tumors; and blood plasma from human subjects.

RESULTS

The sTRA-expressing models tended to have stem-like gene expression and the capacity for mesenchymal differentiation, in contrast to the nonexpressing models. The sTRA cell lines also had significantly increased resistance to seven different chemotherapeutics commonly used against pancreatic cancer. Patients with primary tumors that were positive for a gene expression classifier for sTRA received no statistically significant benefit from adjuvant chemotherapy, in contrast to those negative for the signature. In another cohort, based on direct measurements of sTRA in tissue microarrays, the patients who were high in sTRA again had no statistically significant benefit from adjuvant chemotherapy. Furthermore, a blood plasma test for the sTRA glycan identified the PDACs that showed rapid relapse following neoadjuvant chemotherapy.

CONCLUSIONS

This research demonstrates that a glycan biomarker could have value to detect chemotherapy-resistant PDAC in clinical settings. This capability could aid in the development of stratified treatment plans and facilitate biomarker-guided trials targeting resistant PDAC.

摘要

目的

一小部分胰腺导管腺癌(PDAC)对全身化疗具有高度耐药性,但临床上没有可识别该亚组的标志物。我们假设一种称为唾液酸化肿瘤相关抗原(sTRA)的 PDAC 聚糖标志物可用于此目的。

实验设计

我们在多个系统中测试了根据聚糖表达对 PDAC 进行分类的差异:细胞系、类器官和同基因细胞系集;原发性肿瘤;以及来自人类受试者的血浆。

结果

与非表达模型相比,表达 sTRA 的模型往往具有干细胞样基因表达和间充质分化的能力。sTRA 细胞系对七种常用于治疗胰腺癌的不同化疗药物也具有显著增加的耐药性。与该特征阴性的患者相比,原发性肿瘤对 sTRA 基因表达分类器呈阳性的患者接受辅助化疗没有统计学上的显著获益。在另一队列中,基于组织微阵列中 sTRA 的直接测量,sTRA 水平高的患者也没有从辅助化疗中获得统计学上的显著获益。此外,血浆中 sTRA 糖链的检测可以识别出在新辅助化疗后迅速复发的 PDAC。

结论

这项研究表明,聚糖标志物在临床环境中具有检测化疗耐药性 PDAC 的价值。这种能力可以帮助制定分层治疗计划,并促进针对耐药性 PDAC 的基于生物标志物的试验。