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ZIP7(SLC39A7)在结直肠癌中的表达及其与临床预后的相关性。

ZIP7 (SLC39A7) expression in colorectal cancer and its correlation with clinical prognosis.

作者信息

Luo Yang, Shen Yicheng, Ju Zhong, Zhang Zhi

机构信息

Department of General Surgery, Suzhou Ninth People's Hospital, Suzhou, China.

Department of Dermatology, Suzhou Municipal Hospital, Suzhou, China.

出版信息

Transl Cancer Res. 2020 Oct;9(10):6471-6478. doi: 10.21037/tcr-20-2640.

DOI:10.21037/tcr-20-2640
PMID:35117255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8798949/
Abstract

BACKGROUND

Colorectal cancer (CRC) is a common gastrointestinal malignant tumor that occurs in the colon site and accounts for 9% of the total malignant tumors. Among malignant tumors, its morbidity and mortality respectively rank third and fourth, seriously threatening human health and causing a heavy economic burden on society. ZIP7 (SLC39A7), a kind of zinc transporter, plays a crucial role in the self-renewal of intestinal epithelial cells; however, its role in CRC has not been extensively examined. Therefore, our study aimed to analyze the biological function and expression of this zinc transporter in CRC, along with its correlation with disease activity.

METHODS

In this study, 118 cases of colorectal carcinoma tissues, 30 normal tissue samples from adjacent cancer tissues, and 30 normal intestinal mucosa tissue samples from non-intestinal cancer patients were collected in our hospital between February 2014 and February 2015. The expressions of ZIP7 were examined immunohistochemically, and the relationship between ZIP7 expression and the clinical pathological features of CRC were analyzed. After appropriate surgical treatment, the patients accepted a 5-year follow-up for evaluation of their recurrence situation and 5-year survival rate.

RESULTS

Immunohistochemically, out of 80 CRC tissue samples, 67.8% were found to be positive for ZIP7, 55% (44 cases) were strong positives, and 45% (36 cases) were weak positives. There was a striking coherence between the expression of ZIP7, the depth of lymph node metastasis, CRC invasion, and CRC Dukes stage (P<0.05). Subsequent studies indicated that the mortality rate was positively correlated with the staining intensity of ZIP7 (P<0.05), and the Cox proportional hazards model confirmed that ZIP7 is an independent element of prognostic in patients with CRC (RR =3.896; 95% CI: 1.526-9.951; P=0.004).

CONCLUSIONS

The high expression of ZIP 7 in epithelial cells is related to the clinical stage and prognosis of CRC and can be utilized as a biomarker to predict the prognosis of CRC patients.

摘要

背景

结直肠癌(CRC)是一种常见的胃肠道恶性肿瘤,发生于结肠部位,占全部恶性肿瘤的9%。在恶性肿瘤中,其发病率和死亡率分别位居第三和第四,严重威胁人类健康,并给社会带来沉重的经济负担。ZIP7(SLC39A7)是一种锌转运蛋白,在肠道上皮细胞的自我更新中起关键作用;然而,其在结直肠癌中的作用尚未得到广泛研究。因此,我们的研究旨在分析这种锌转运蛋白在结直肠癌中的生物学功能和表达情况,以及其与疾病活动的相关性。

方法

本研究收集了2014年2月至2015年2月期间我院的118例结直肠癌组织、30例来自癌旁组织的正常组织样本以及30例非结直肠癌患者的正常肠黏膜组织样本。采用免疫组织化学方法检测ZIP7的表达情况,并分析ZIP7表达与结直肠癌临床病理特征之间的关系。经过适当的手术治疗后,对患者进行5年随访,以评估其复发情况和5年生存率。

结果

免疫组织化学检测显示,在80例结直肠癌组织样本中,67.8%的样本ZIP7呈阳性,55%(44例)为强阳性,45%(36例)为弱阳性。ZIP7的表达与淋巴结转移深度、结直肠癌侵袭及结直肠癌Dukes分期之间存在显著相关性(P<0.05)。后续研究表明,死亡率与ZIP7的染色强度呈正相关(P<0.05),Cox比例风险模型证实ZIP7是结直肠癌患者预后的独立因素(RR =3.896;95%CI:1.526 - 9.951;P=0.004)。

结论

ZIP7在上皮细胞中的高表达与结直肠癌的临床分期和预后相关,可作为预测结直肠癌患者预后的生物标志物。

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本文引用的文献

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A novel cancer stem cell-based classification model for the tumorigenesis and development of colorectal cancer.一种基于新型癌症干细胞的结直肠癌肿瘤发生与发展分类模型。
Transl Cancer Res. 2019 Nov;8(7):2621-2623. doi: 10.21037/tcr.2019.10.19.
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An early report of a screening program for colorectal cancer in Guangzhou, China.中国广州一项结直肠癌筛查项目的早期报告。
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Cancer statistics, 2020.癌症统计数据,2020 年。
CA Cancer J Clin. 2020 Jan;70(1):7-30. doi: 10.3322/caac.21590. Epub 2020 Jan 8.
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Comprehensive clinical genetics care for patients with inherited colorectal cancer associated with Lynch syndrome: Western and Asian perspectives.林奇综合征相关遗传性结直肠癌患者的综合临床遗传学护理:西方和亚洲视角
Chin Clin Oncol. 2018 Feb;7(1):9. doi: 10.21037/cco.2018.01.06.
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Proportion and number of cancer cases and deaths attributable to potentially modifiable risk factors in the United States.美国可改变的潜在风险因素导致的癌症病例和死亡人数及比例。
CA Cancer J Clin. 2018 Jan;68(1):31-54. doi: 10.3322/caac.21440. Epub 2017 Nov 21.
6
Knockdown of SLC39A7 inhibits cell growth and induces apoptosis in human colorectal cancer cells.敲低 SLC39A7 抑制人结直肠癌细胞的生长并诱导其凋亡。
Acta Biochim Biophys Sin (Shanghai). 2017 Oct 1;49(10):926-934. doi: 10.1093/abbs/gmx094.
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Colorectal cancer statistics, 2017.结直肠癌统计数据,2017 年。
CA Cancer J Clin. 2017 May 6;67(3):177-193. doi: 10.3322/caac.21395. Epub 2017 Mar 1.
8
Phosphorylation of zinc channel ZIP7 drives MAPK, PI3K and mTOR growth and proliferation signalling.锌通道ZIP7的磷酸化驱动丝裂原活化蛋白激酶(MAPK)、磷脂酰肌醇-3-激酶(PI3K)和哺乳动物雷帕霉素靶蛋白(mTOR)的生长及增殖信号传导。
Metallomics. 2017 May 24;9(5):471-481. doi: 10.1039/c6mt00286b.
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Cancer Statistics, 2017.《2017 年癌症统计》
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