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CD44-rs353630 和 CHI3L2-rs684559 与胰腺导管腺癌生存无关联。

Lack of association of CD44-rs353630 and CHI3L2-rs684559 with pancreatic ductal adenocarcinoma survival.

机构信息

Department of Biology, University of Pisa, Via Derna 1, 56126, Pisa, Italy.

Pancreato-Biliary Endoscopy and Endosonography Division, Pancreas Translational and Clinical Research Center, IRCCS San Raffaele Scientific Institute, Milan, Italy.

出版信息

Sci Rep. 2021 Apr 7;11(1):7570. doi: 10.1038/s41598-021-87130-0.

Abstract

Although pancreatic ductal adenocarcinoma (PDAC) survival is poor, there are differences in patients' response to the treatments. Detection of predictive biomarkers explaining these differences is of the utmost importance. In a recent study two genetic markers (CD44-rs353630 and CHI3L2-rs684559) were reported to be associated with survival after PDAC resection. We attempted to replicate the associations in 1856 PDAC patients (685 resected with stage I/II) from the PANcreatic Disease ReseArch (PANDoRA) consortium. We also analysed the combined effect of the two genotypes in order to compare our results with what was previously reported. Additional stratified analyses considering TNM stage of the disease and whether the patients received surgery were also performed. We observed no statistically significant associations, except for the heterozygous carriers of CD44-rs353630, who were associated with worse OS (HR = 5.01; 95% CI 1.58-15.88; p = 0.006) among patients with stage I disease. This association is in the opposite direction of those reported previously, suggesting that data obtained in such small subgroups are hardly replicable and should be considered cautiously. The two polymorphisms combined did not show any statistically significant association. Our results suggest that the effect of CD44-rs353630 and CHI3L2-rs684559 cannot be generalized to all PDAC patients.

摘要

虽然胰腺导管腺癌 (PDAC) 的生存率较差,但患者对治疗的反应存在差异。检测解释这些差异的预测生物标志物至关重要。在最近的一项研究中,报告了两个遗传标记物 (CD44-rs353630 和 CHI3L2-rs684559) 与 PDAC 切除术后的生存相关。我们试图在来自 PANcreatic Disease ReseArch (PANDoRA) 联盟的 1856 名 PDAC 患者(685 名接受 I/II 期手术)中复制这些关联。我们还分析了两种基因型的联合效应,以便将我们的结果与之前报道的结果进行比较。还考虑了疾病的 TNM 分期以及患者是否接受手术等因素进行了分层分析。我们没有观察到统计学上显著的关联,除了 CD44-rs353630 的杂合子携带者,他们与 I 期疾病患者的 OS 较差相关(HR=5.01;95%CI 1.58-15.88;p=0.006)。这种关联与之前报道的相反,表明在如此小的亚组中获得的数据几乎无法复制,应谨慎考虑。两种多态性的组合没有显示出任何统计学上显著的关联。我们的结果表明,CD44-rs353630 和 CHI3L2-rs684559 的影响不能推广到所有 PDAC 患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf0f/8027406/80d3af88d86e/41598_2021_87130_Fig1_HTML.jpg

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