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人平衡核苷转运体1:吉西他滨治疗的胰腺癌患者的新型生物标志物和预后指标。

Human Equilibrative Nucleoside Transporter 1: Novel Biomarker and Prognostic Indicator for Patients with Gemcitabine-Treated Pancreatic Cancer.

作者信息

Xiao Jianchun, Zhao Fangyu, Luo Wenhao, Yang Gang, Wang Yicheng, Qiu Jiangdong, Liu Yueze, You Lei, Zheng Lianfang, Zhang Taiping

机构信息

Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, People's Republic of China.

Department of Nuclear Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, People's Republic of China.

出版信息

Cancer Manag Res. 2024 Jun 21;16:651-661. doi: 10.2147/CMAR.S465098. eCollection 2024.

Abstract

AIM

This article aimed to find appropriate pancreatic cancer (PC) patients to treat with Gemcitabine with better survival outcomes by detecting hENT1 levels.

METHODS

We collected surgical pathological tissues from PC patients who received radical surgery in our hospital from September 2004 to December 2014. A total of 375 PC tissues and paired adjacent nontumor tissues were employed for the construction of 4 tissue microarrays (TMAs). The quality of the 4 TMAs was examined by HE staining. We performed immunohistochemistry analysis to evaluate hENT1 expression in the TMAs. Moreover, we detected hENT1 expression level and proved the role of hENT1 in cell proliferation, drug resistance, migration and invasion in vivo and vitro.

RESULTS

The results indicated that low hENT1 expression indicated a significantly poor outcome in PC patients, including shortened DFS (21.6±2.8 months versus 36.9±4.0 months, p<0.001) and OS (33.6±3.9 versus 39.6±3.9, p=0.004). Meanwhile, patients in stage I/II of TNM stage had a longer OS (40.2±3.4 versus 15.4±1.7, p=0.002) and DFS (31.0±3.1 versus 12.4±1.9, p=0.016) than patients in stage III/IV. Patients in M0 stage had a longer OS (39.7±3.4 versus 16.2±1.9, p=0.026) and DFS(30.7±3.0 versus 11.8±2.2, p=0.031) than patients in M1 stage, and patients with tumors not invading the capsule had a better DFS than those with tumor invasion into the capsule (30.8±3.0 versus 12.6±2.3, p=0.053). Patients with preoperative CA19-9 values ≤467 U/mL have longer DFS than that of patients who had preoperative CA19-9 values >467 U/mL (37.9±4.1 versus 22.9±4.0, p=0.04). In the subgroup analysis, a high hENT1 expression level was related to a longer OS(39.4±4.0 versus 31.5±3.9, p=0.001) and DFS(35.7±4.0 versus 20.6±2.7; p<0.0001) in the Gemcitabine subgroup.

CONCLUSION

PC patients with high hENT1 expression have a better survival outcomes when receiving Gemcitabine. hENT1 expression can be a great prognostic indicator for PC patients to receive Gemcitabine treatment.

摘要

目的

本文旨在通过检测人等效核苷转运体1(hENT1)水平,寻找适合接受吉西他滨治疗且生存结局更佳的胰腺癌(PC)患者。

方法

收集2004年9月至2014年12月在我院接受根治性手术的PC患者的手术病理组织。共采用375份PC组织及配对的相邻非肿瘤组织构建4个组织芯片(TMA)。通过苏木精-伊红(HE)染色检查4个TMA的质量。我们进行免疫组织化学分析以评估TMA中hENT1的表达。此外,我们检测hENT1表达水平,并证实hENT1在体内外细胞增殖、耐药性、迁移和侵袭中的作用。

结果

结果表明,hENT1低表达表明PC患者的结局显著较差,包括无病生存期(DFS)缩短(21.6±2.8个月对36.9±4.0个月,p<0.001)和总生存期(OS)缩短(33.6±3.9对39.6±3.9,p=0.004)。同时,TNM分期为I/II期的患者比III/IV期患者的OS更长(40.2±3.4对15.4±1.7,p=0.002)和DFS更长(31.0±3.1对12.4±1.9,p=0.016)。M0期患者比M1期患者的OS更长(39.7±3.4对16.2±1.9,p=0.026)和DFS更长(30.7±3.0对11.8±2.2,p=0.031),且肿瘤未侵犯包膜的患者比肿瘤侵犯包膜的患者DFS更好(30.8±3.0对12.6±2.3,p=0.053)。术前CA19-9值≤467 U/mL的患者比术前CA19-9值>467 U/mL的患者DFS更长(37.9±4.1对22.9±4.0,p=0.04)。在亚组分析中,吉西他滨亚组中hENT1高表达水平与更长的OS(39.4±4.0对31.5±3.9,p=0.001)和DFS(35.7±4.0对20.6±2.7;p<0.0001)相关。

结论

hENT1高表达的PC患者接受吉西他滨治疗时生存结局更佳。hENT1表达可作为PC患者接受吉西他滨治疗的重要预后指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d82f/11198018/ff8ecf4cd79b/CMAR-16-651-g0001.jpg

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