期刊文献+

量子点免疫荧光成像技术同步检测乳腺癌黏蛋白1及Ⅳ型胶原蛋白的临床意义

Clinical significances of the synchronous detection of mucin 1 and collagen Ⅳ in breast cancer by using quantum dots immunofluorescence imaging technique
原文传递
导出
摘要 目的利用量子点免疫荧光成像技术,探讨黏蛋白1及Ⅳ型胶原蛋白与浸润性乳腺癌临床病理特征的关系。方法应用量子点免疫荧光成像技术和免疫组织化学技术检测2007年7月至2010年7月桂林医学院附属医院收治的94例乳腺癌组织中黏蛋白1及Ⅳ型胶原蛋白的表达,分析黏蛋白1及Ⅳ型胶原蛋白定量参数与乳腺癌患者临床病理特征的相关性及其与预后的关系。结果量子点免疫荧光成像技术和免疫组织化学技术标记人乳腺癌组织中黏蛋白1阳性率分别为73.4 %(69/94)、69.1 %(65/94),Ⅳ型胶原蛋白阳性率分别为53.2 %(50/94)、47.9 %(45/94),差异均无统计学意义(均P〉0.05),两种方法标记的效果具有一致性(κ=0.763,P=0.000;κ=0.759,P=0.000)。分析量子点免疫荧光成像技术检测结果,黏蛋白1与Ⅳ型胶原蛋白的表达呈负相关(r=-0.883,P〈0.01);黏蛋白1和Ⅳ型胶原蛋白的表达与肿瘤大小(F=3.683,P=0.029;F=4.922,P=0.009)、组织学分级(F=3.529,P=0.033;F=3.912,P=0.023)、淋巴结转移(t=-4.868,P=0.000;t=3.868,P=0.000)、病理分期(t=-8.337,P=0.000;t=5.962,P=0.000)和5年无病生存率(均P=0.000)均有相关性。结论利用量子点免疫荧光成像技术可同时检测黏蛋白1及Ⅳ型胶原蛋白,可为乳腺癌生物学行为及预后判断提供依据。 ObjectiveTo investigate the relationship between the expression of mucin 1 and collagen Ⅳ and the clinical characteristics in invasive breast cancer by using the quantum dots immunofluorescence imaging technique.MethodsThe expressions of mucin 1 and collagen Ⅳ were detected simultaneously by quantum dots immunofluorescence imaging technique in 94 cases of breast cancer from July 2007 to July 2010 in Affiliated Hospital of Guilin Medical University. The correlation of mucin 1 and collagen Ⅳ quantitative parameters with clinicopathological features and the prognosis were also analyzed.ResultsThe positive rates of mucin 1 in human breast cancer tissues marked by quantum dots immunofluorescence imaging technique and immunohistochemistry were 73.4 % (69/94) and 69.1 % (65/94), the positive rates of collagen Ⅳ were 53.2 % (50/94) and 47.9 % (45/94), and the differences were not statistically significant (both P 〉 0.05) Quantum dots immunofluorescence imaging technique was consistent with conventional immunohistochemistry (IHC) in detecting the expressions of mucin 1 and collagen Ⅳ in human breast cancer tissues (κ = 0.763, P = 0.000; κ=0.759, P = 0.000). The expression of mucin 1 was negatively correlated with collagen Ⅳ (r = -0.883, P 〈 0.01). The expressions of mucin 1 and collagen Ⅳ were respectively associated with tumor size (F = 3.683, P = 0.029; F = 4.922, P = 0.009), histological grading (F = 3.529, P = 0.033; F = 3.912, P = 0.023), lymph node metastasis (t = -4.868, P = 0.000; t = 3.868, P = 0.000), pathological stage (t = -8.337, P = 0.000; t = 5.962, P = 0.000) and 5-year disease free survival rate (both P = 0.000), and the differences were statistically significant (all P 〈 0.05).ConclusionThe co-detection of mucin 1 and collagen Ⅳ by using quantum dots immunofluorescence imaging technique provides direct evidence determining the biologic behaviors of breast cancer and evaluating the prognosis.
作者 刘秀丽 柳正春 王振华 康马飞 Liu Xiuli;Liu Zhengchun;Wang Zhenhua;Kang Mafei(Department of Oncology,Affiliated Hospital of Guilin Medical University,Guilin 541001,China;Department of Radiation Oncology,Affiliated Hospital of Guilin Medical University,Guilin 541001,China;Department of Minimally Invasive Digestive Surgery,Affiliated Cancer Hospital of Shanxi Medical University,Taiyuan 030013,China)
出处 《肿瘤研究与临床》 CAS 2018年第8期505-510,共6页 Cancer Research and Clinic
基金 广西自然科学基金面上项目(2016GXNSFAA380306) 广西自然科学基金青年基金(2015GXNSFBA139151) 广西壮族自治区卫生和计划生育委员会课题(Z2015385、Z20170816)
关键词 乳腺肿瘤 黏蛋白1 Ⅳ型胶原 量子点 Breast neoplasms Mucin 1 Collagen Ⅳ Quantum dots
  • 相关文献

参考文献2

二级参考文献32

  • 1Walling MA, Novak JA, Shepard JR. Quantum dots for live cell and in vivo imaging. Int J Mol Sci, 2009, 10: 441-491.
  • 2Zhang H, Sachdev D, Wang C, et al. Detection and downregulation of type I IGF receptor expression by antibody-conjugated quantum dots in breast cancer cells. Breast Cancer Res Treat, 2009, 114: 277-285.
  • 3Snyder EL, Bailey D, Shipitsin M, et al. Identification of CD44v6(+) /CD24-breast carcinoma cells in primary human tumors by quantum dot-conjugated antibodies. Lab Invest, 2009, 89: 857-866.
  • 4Chen C, Peng J, Xia HS, et al. Quantum dots-based immunofluore-scence technology for the quantitative determination of HER2 expression in breast cancer. Biomaterials, 2009, 30: 2912-2918.
  • 5Cheng AK, Su H, Wang YA, et al. Aptamer-based detection of epithelial tumor marker mucin I with quantum dot-based fluorescence readout. Anal Chore, 2009, 81: 6130-6139.
  • 6Smith AM, Duan H, Mohs AM, et al. Bioconjugated quantum dots for in vivo molecular and cellular imaging. Adv Drug Deliv Rev, 2008, 60: 1226-1240.
  • 7Papagiannaros A, Levchenko T, Hartner W, et al. Quantum dots encapsulated in phospholipid micelles for imaging and quantification of tumors in the near-infrared region. Nanomedicine, 2009, 5: 216-224.
  • 8Weng KC, Noble CO, Papahadjopoulos-Sternberg B, et al. Targeted tumor cell internalization and imaging of muhifunctional quantum dot-conjugated immunoliposomes in vitro and in vivo. Nano Lett, 2008, 8: 2851-2857.
  • 9Tada H, Higuchi H, Wanatabe TM, et al. In vivo real-time tracking of single quantum dots conjugated with monoclonal ani-HER2 antibody in tumors of mice. Cancer Res, 2007, 67:1138-1144.
  • 10Cai W, Chen X. Preparation ofpeptide-conjugated quantum dots for tum.r vasculature-targeted imaging. Nat Protoc, 2008, 3: 89-96.

共引文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部