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A Review of Podocyte Biology.足细胞生物学研究进展综述。
Am J Nephrol. 2018;47 Suppl 1:3-13. doi: 10.1159/000481633. Epub 2018 May 31.
2
Clinical applications of urinary cell-free DNA in cancer: current insights and promising future.尿游离DNA在癌症中的临床应用:当前见解与光明前景
Am J Cancer Res. 2017 Nov 1;7(11):2318-2332. eCollection 2017.
3
Non-blood circulating tumor DNA detection in cancer.癌症中循环肿瘤非血液DNA检测
Oncotarget. 2017 Aug 4;8(40):69162-69173. doi: 10.18632/oncotarget.19942. eCollection 2017 Sep 15.
4
Gemcitabine combined with the monoclonal antibody nimotuzumab is an active first-line regimen in KRAS wildtype patients with locally advanced or metastatic pancreatic cancer: a multicenter, randomized phase IIb study.吉西他滨联合单克隆抗体尼妥珠单抗是 KRAS 野生型局部晚期或转移性胰腺癌患者的一线有效方案:一项多中心、随机、Ⅱb 期研究。
Ann Oncol. 2017 Oct 1;28(10):2429-2435. doi: 10.1093/annonc/mdx343.
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Utility of urinary circulating tumor DNA for EGFR mutation detection in different stages of non-small cell lung cancer patients.尿液循环肿瘤 DNA 检测在非小细胞肺癌不同分期患者 EGFR 突变中的应用。
Clin Transl Oncol. 2017 Oct;19(10):1283-1291. doi: 10.1007/s12094-017-1669-3. Epub 2017 May 11.
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Dynamic tracing for epidermal growth factor receptor mutations in urinary circulating DNA in gastric cancer patients.胃癌患者尿液循环DNA中表皮生长因子受体突变的动态追踪
Tumour Biol. 2017 Feb;39(2):1010428317691681. doi: 10.1177/1010428317691681.
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Utility of serum DNA as a marker for KRAS mutations in pancreatic cancer tissue.血清DNA作为胰腺癌组织中KRAS突变标志物的效用。
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Investigation of transrenal KRAS mutation in late stage NSCLC patients correlates to disease progression.晚期非小细胞肺癌患者经肾KRAS突变的研究与疾病进展相关。
Biomarkers. 2017 Nov;22(7):654-660. doi: 10.1080/1354750X.2016.1269202. Epub 2016 Dec 21.
9
The potential use of urine cell free DNA as a marker for cancer.尿液游离 DNA 作为癌症标志物的潜在用途。
Expert Rev Mol Diagn. 2016 Dec;16(12):1283-1290. doi: 10.1080/14737159.2016.1254551. Epub 2016 Nov 10.
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A Highly Sensitive and Quantitative Test Platform for Detection of NSCLC EGFR Mutations in Urine and Plasma.一种用于检测尿液和血浆中 NSCLC EGFR 突变的高灵敏度和定量检测平台。
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液体活检在胰腺导管腺癌患者中应用的实用性。

Utility of liquid biopsy using urine in patients with pancreatic ductal adenocarcinoma.

机构信息

Department of Gastroenterology and Hepatology, Dentistry and Pharmaceutical Sciences, Okayama University Graduate School of Medicine , Okayama , Japan.

出版信息

Cancer Biol Ther. 2019;20(10):1348-1353. doi: 10.1080/15384047.2019.1638685. Epub 2019 Jul 22.

DOI:10.1080/15384047.2019.1638685
PMID:31328611
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6783121/
Abstract

In recent years, liquid biopsy for blood and body fluid in cancer patients has attracted attention. However, there have been few reports of liquid biopsy focusing on urine of pancreatic ductal adenocarcinoma (PDAC). In 56 patients with PDAC, DNA was extracted from urine and plasma prior to treatment, and KRAS mutations were analyzed with droplet digital PCR to examine the mutation detection rate. Our study showed that KRAS mutations were found in 27 cases (48%) in urine and 27 cases (48%) in plasma. The detection rate of urine KRAS mutations varied by renal functions. The rates were 70% (14/20) and 36% (13/36) in the creatinine clearance rate (CCr) < 70 mL/min group and in the CCr ≥ 70 mL/min group, respectively ( = .024). Whereas, no influence of the CCr was observed in the detection rates of plasma KRAS mutations. The rates were 50% (10/20) and 47% (17/36) in cases with the CCr < 70 mL/min group and the CCr ≥ 70 mL/min group, respectively. Although the sample size was small, this study clearly indicated a new possibility of less invasive urine liquid biopsy in PDAC patients.

摘要

近年来,针对癌症患者血液和体液的液体活检受到了关注。然而,针对胰腺导管腺癌(PDAC)尿液的液体活检研究较少。本研究对 56 例 PDAC 患者进行了前瞻性研究,在治疗前分别从尿液和血浆中提取 DNA,采用液滴数字 PCR 分析 KRAS 基因突变,以检测突变的检出率。我们的研究表明,尿液中 KRAS 基因突变 27 例(48%),血浆中 KRAS 基因突变 27 例(48%)。尿液 KRAS 基因突变的检出率与肾功能有关。在 CCr<70ml/min 组和 CCr≥70ml/min 组,其检出率分别为 70%(14/20)和 36%(13/36)(=0.024)。而血浆 KRAS 基因突变的检出率不受 CCr 的影响。在 CCr<70ml/min 组和 CCr≥70ml/min 组,其检出率分别为 50%(10/20)和 47%(17/36)。尽管样本量较小,但本研究清楚地表明 PDAC 患者进行微创性尿液液体活检具有新的可能性。