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利用CRP 1846C>T基因多态性评估浸润性乳腺癌淋巴结转移的可能性。

Evaluation of the potential for lymph node metastasis using CRP 1846C>T genetic polymorphism in invasive breast cancer.

作者信息

Terata Kaori, Motoyama Satoru, Kamata Shuichi, Hinai Yudai, Miura Masatomo, Sato Yusuke, Yoshino Kei, Ito Aki, Imai Kazuhiro, Saito Hajime, Minamiya Yoshihiro

机构信息

Division of Brest Surgery, Akita Red Cross Hospital, Akita, Japan.

出版信息

Tumour Biol. 2014 Jun;35(6):5931-5. doi: 10.1007/s13277-014-1786-3. Epub 2014 Mar 16.

DOI:10.1007/s13277-014-1786-3
PMID:24633920
Abstract

Lymph node status is a key indicator of the best approach to treatment of invasive breast cancer. However, the accuracy with which lymph node metastasis is diagnosed is not currently satisfactory. New and more reliable methods that enable one to know who has a greater potential for lymph node metastasis would be highly desirable. We previously reported that lymph node involvement in esophageal and lung cancer may have a genetic component: C-reactive protein (CRP) 1846C>T genetic polymorphism. Here we examined the diagnostic value of CRP 1846C>T polymorphism for assessing the risk of lymph node metastasis in cases of invasive breast cancer. The study participants were 185 women with invasive breast cancer who underwent curative surgery with lymph node dissection. Using DNA from blood samples and polymerase chain reaction-restriction fragment length polymorphism, the utility of CRP genetic 1846C>T polymorphism (rs1205) for assessing the risk of lymph node metastasis was evaluated. Fifty-two (28 %) patients had lymph node metastasis. After the patients were divided into two groups based on their CRP 1846 genotypes (C/C+C/T and T/T), the clinical characteristics did not differ between the groups, but there was a significantly greater incidence of lymph node metastasis among patients in the T/T group. Moreover, the odds ratio for lymph node involvement in patients carrying the 1846 T/T genotype was more than 2.2 in multivariate logistic regression models. CRP genetic polymorphism may be a novel predictor of the risk of lymph node metastasis in invasive breast cancer.

摘要

淋巴结状态是浸润性乳腺癌最佳治疗方法的关键指标。然而,目前诊断淋巴结转移的准确性并不令人满意。非常需要新的、更可靠的方法来确定谁有更高的淋巴结转移可能性。我们之前报道过,食管癌和肺癌中的淋巴结受累可能有遗传因素:C反应蛋白(CRP)1846C>T基因多态性。在此,我们研究了CRP 1846C>T多态性对评估浸润性乳腺癌患者淋巴结转移风险的诊断价值。研究对象为185例接受了淋巴结清扫根治性手术的浸润性乳腺癌女性患者。利用血样中的DNA和聚合酶链反应-限制性片段长度多态性技术,评估了CRP基因1846C>T多态性(rs1205)对评估淋巴结转移风险的实用性。52例(28%)患者发生了淋巴结转移。根据患者的CRP 1846基因型(C/C+C/T和T/T)将患者分为两组后,两组的临床特征无差异,但T/T组患者的淋巴结转移发生率显著更高。此外,在多因素逻辑回归模型中,携带1846 T/T基因型患者发生淋巴结受累的比值比超过2.2。CRP基因多态性可能是浸润性乳腺癌淋巴结转移风险的一种新的预测指标。

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本文引用的文献

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C-reactive protein inhibits lymphangiogenesis and resultant lymph node metastasis of squamous cell carcinoma in mice.C 反应蛋白抑制小鼠鳞状细胞癌的淋巴管生成和由此导致的淋巴结转移。
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Evaluation of the risk of lymph node metastasis using CRP 1846C>T genetic polymorphism in submucosal thoracic esophageal squamous cell carcinoma.采用 CRP1846C>T 基因多态性评估黏膜下胸段食管鳞癌的淋巴结转移风险。
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Biosci Rep. 2019 Jun 20;39(6). doi: 10.1042/BSR20181936. Print 2019 Jun 28.
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C-reactive protein inhibits expression of N-cadherin and ZEB-1 in murine colon adenocarcinoma.C反应蛋白抑制小鼠结肠腺癌中N-钙黏蛋白和锌指蛋白E盒结合因子1的表达。
Tumour Biol. 2015 Sep;36(9):7035-43. doi: 10.1007/s13277-015-3414-2. Epub 2015 Apr 13.
新诊断乳腺癌患者腋窝淋巴结的影像学检查
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Metastasis-related miRNAs, active players in breast cancer invasion, and metastasis.转移相关的 microRNAs,乳腺癌侵袭和转移的活跃参与者。
Cancer Metastasis Rev. 2010 Dec;29(4):785-99. doi: 10.1007/s10555-010-9265-9.
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The role of ultrasonography and FDG-PET in axillary lymph node staging of breast cancer.超声检查和氟代脱氧葡萄糖正电子发射断层扫描在乳腺癌腋窝淋巴结分期中的作用。
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A multicenter cohort study to compare quality of life in breast cancer patients according to sentinel lymph node biopsy or axillary lymph node dissection.一项多中心队列研究,旨在根据前哨淋巴结活检或腋窝淋巴结清扫比较乳腺癌患者的生活质量。
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