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ADAMTS5的高表达是结直肠癌淋巴管侵犯和淋巴结转移的有力标志物。

High expression of ADAMTS5 is a potent marker for lymphatic invasion and lymph node metastasis in colorectal cancer.

作者信息

Haraguchi Naotsugu, Ohara Nobuyoshi, Koseki Jun, Takahashi Hidekazu, Nishimura Junichi, Hata Taishi, Mizushima Tsunekazu, Yamamoto Hirofumi, Ishii Hideshi, Doki Yuichiro, Mori Masaki

机构信息

Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.

Department of Cancer Profiling Discovery, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.

出版信息

Mol Clin Oncol. 2017 Jan;6(1):130-134. doi: 10.3892/mco.2016.1088. Epub 2016 Nov 21.

DOI:10.3892/mco.2016.1088
PMID:28123746
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5244970/
Abstract

Members of the ADAMTS family contain propeptide, metalloproteinase and disintegrin domains and serve key roles for cancer cell proliferation, progression and metastasis. Although overexpression of ADAMTS5 has been reported in glioblastoma, and head and neck cancer, little has been demonstrated in colorectal cancer types. The present study aimed to clarify the significance of ADAMTS5 for clinicopathological factors and prognosis in colorectal cancer. The mRNA expression of ADAMTS5 was measured in 143 colorectal cancer specimens. ADAMTS5 expression was increased as the pathological stage increased. The expression of ADAMTS5 in stage III-IV colorectal cancer was significantly greater compared with that of stage 0-II colorectal cancer (P=0.0003). The median expression of ADAMTS5 was used to divide the ADAMTS5 higher expressing group and the ADAMTS5 lower expressing group to assess the correlation of ADAMTS5 expression with clinicopathological factors and prognosis. The proportions of lymphatic invasion and lymph node metastasis were significantly greater in the ADAMTS5 higher expressing group (P=0.0214 and P=0.0289 respectively). Overall survival and disease-free survival were assessed by the Kaplan-Meier curve with calculation of significance by the log-rank test; however, no significant difference was observed between the ADAMTS5 higher expressing group and the ADAMTS5 lower expressing group (P=0.7490 and P=0.9455, respectively). The present study confirmed high expression of ADAMTS5 as a potent marker for lymphatic invasion and lymphnode metastasis in colorectal cancer. To clarify the function of ADAMTS5 in colorectal cancer, further molecular investigations are required.

摘要

ADAMTS家族成员包含前肽、金属蛋白酶和解聚素结构域,在癌细胞增殖、进展和转移中发挥关键作用。尽管已有报道称ADAMTS5在胶质母细胞瘤、头颈癌中过表达,但在结直肠癌类型中鲜有相关研究。本研究旨在阐明ADAMTS5在结直肠癌临床病理因素及预后中的意义。对143例结直肠癌标本检测ADAMTS5的mRNA表达。ADAMTS5表达随病理分期增加而升高。III-IV期结直肠癌中ADAMTS5的表达显著高于0-II期结直肠癌(P=0.0003)。以ADAMTS5的中位表达量将其分为高表达组和低表达组,评估ADAMTS5表达与临床病理因素及预后的相关性。ADAMTS5高表达组的淋巴侵犯和淋巴结转移比例显著更高(分别为P=0.0214和P=0.0289)。采用Kaplan-Meier曲线评估总生存期和无病生存期,并通过对数秩检验计算显著性;然而,ADAMTS5高表达组和低表达组之间未观察到显著差异(分别为P=0.7490和P=0.9455)。本研究证实ADAMTS5高表达是结直肠癌淋巴侵犯和淋巴结转移的有效标志物。为阐明ADAMTS5在结直肠癌中的功能,需要进一步开展分子研究。

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本文引用的文献

1
Global Cancer Incidence and Mortality Rates and Trends--An Update.全球癌症发病率、死亡率及趋势——最新情况
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2
The Evolving Scale and Profile of Cancer Worldwide: Much Ado About Everything.全球癌症规模与概况的演变:小题大做?
Cancer Epidemiol Biomarkers Prev. 2016 Jan;25(1):3-5. doi: 10.1158/1055-9965.EPI-15-1109. Epub 2015 Dec 14.
3
Regorafenib monotherapy for previously treated metastatic colorectal cancer (CORRECT): an international, multicentre, randomised, placebo-controlled, phase 3 trial.regorafenib 单药治疗既往治疗的转移性结直肠癌(CORRECT):一项国际、多中心、随机、安慰剂对照、3 期临床试验。
Lancet. 2013 Jan 26;381(9863):303-12. doi: 10.1016/S0140-6736(12)61900-X. Epub 2012 Nov 22.
4
Emerging roles for ADAMTS5 during development and disease.ADAMTS5在发育和疾病过程中的新作用。
Matrix Biol. 2011 Jun;30(5-6):311-7. doi: 10.1016/j.matbio.2011.05.004. Epub 2011 Jun 12.
5
Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008.2008 年全球癌症负担估计值:GLOBOCAN 2008。
Int J Cancer. 2010 Dec 15;127(12):2893-917. doi: 10.1002/ijc.25516.
6
Epigenomic analysis of aberrantly methylated genes in colorectal cancer identifies genes commonly affected by epigenetic alterations.结直肠癌中异常甲基化基因的表观基因组分析确定了受表观遗传改变共同影响的基因。
Ann Surg Oncol. 2011 Aug;18(8):2338-47. doi: 10.1245/s10434-011-1573-y. Epub 2011 Feb 5.
7
Recent trends in colorectal cancer mortality in Europe.欧洲结直肠癌死亡率的最新趋势。
Int J Cancer. 2011 Jul 1;129(1):180-91. doi: 10.1002/ijc.25653. Epub 2010 Nov 16.
8
Colorectal cancer.结直肠癌。
Lancet. 2010 Mar 20;375(9719):1030-47. doi: 10.1016/S0140-6736(10)60353-4.
9
Annual report to the nation on the status of cancer, 1975-2006, featuring colorectal cancer trends and impact of interventions (risk factors, screening, and treatment) to reduce future rates.国家癌症报告:1975-2006 年,重点介绍结直肠癌的流行趋势和干预措施(危险因素、筛查和治疗)对降低未来发病率的影响
Cancer. 2010 Feb 1;116(3):544-73. doi: 10.1002/cncr.24760.
10
Experimentally derived metastasis gene expression profile predicts recurrence and death in patients with colon cancer.实验得出的转移基因表达谱可预测结肠癌患者的复发和死亡。
Gastroenterology. 2010 Mar;138(3):958-68. doi: 10.1053/j.gastro.2009.11.005. Epub 2009 Nov 13.