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乳腺浸润性导管癌不同分子分型中CD90的表达及其意义 被引量:5

Expression of CD90 and its clinical significance in different molecular subtypes of breast invasive ductal carcinoma
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摘要 目的探讨CD90在乳腺浸润性导管癌中的表达及其与临床病理特征、分子分型的相关性。方法构建80例乳腺浸润性导管癌和20例乳腺良性病变的组织芯片,采用免疫组化Max Vision法检测乳腺不同病变组织中CD90、ER、PR、Ki-67和HER-2的表达水平,并进一步分析其相关性。结果 CD90在乳腺浸润性导管癌和乳腺良性病变中的阳性率分别为62.5%和20.0%,两者差异有统计学意义(P<0.001);CD90表达与乳腺浸润性导管癌淋巴结转移相关(P<0.05),与患者年龄、肿瘤大小、TNM分期及组织学分级无关(P>0.05);在乳腺浸润性导管癌不同分子亚型中,CD90阳性率以Luminal A型最低(40.0%)、三阴型最高(82.4%),各亚型之间差异有统计学意义(P<0.05);CD90与ER(r=-0.342,P<0.05)、PR(r=-0.374,P<0.05)表达呈负相关,与Ki-67表达之间无相关性(r=0.084,P>0.05)。结论 CD90表达与乳腺癌分子分型有关,其高表达提示患者预后不良。 Purpose To detect the expression of CD90 in invasive ductal breast carcinoma with different molecular subtypes and to explore its clinical significance. Methods The expression of CD90, ER, PR, Ki-67 and HER-2 were detected in 80 cases of invasive ductal breast carcinoma tissue and 20 cases of breast benign lesion with immunohistochemical method. The relationship between CD90 and clinicopathological parameters were analyzed. Results The positive expression rate of CD90 in invasive ductal breast carcinoma and breast benign lesion tissues were 62. 5% and 20. 0% , respectively ( P 〈 0. 001 ). The expression of CD90 in invasive ductal breast carcinoma was correlated with lymph node metastasis ( P 〈 0. 05 ), but not with age, tumor size, TNM staging and histological grade( P 〉 0. 05 ). Among different molecular subtypes, CD90 expression level in Luminal A type was the lowest (40. 0% ), and the level in triple negative type was the highest (82.4%) (P 〈 0. 05). CD90 expression level was negatively correlated with ER (r= -0.342, P〈0.05) or PR (r = -0. 374, P 〈0.05) expression level, but not with Ki-67 ( r = 0. 084, P 〉 0. 05 ). Conclusion The over-expression of CD90 is related with molecular subtypes of breast carcinoma, and its high expression suggests a poor prognosis.
出处 《临床与实验病理学杂志》 CAS CSCD 北大核心 2017年第3期245-249,共5页 Chinese Journal of Clinical and Experimental Pathology
基金 江西省卫生厅科技计划(20143006)
关键词 乳腺肿瘤 CD90 分子分型 转移 免疫组织化学 breast neoplasm CD90 molecular subtyping metastasis immunohistochemistry
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  • 1江泽飞,宋三泰,孙燕.乳腺癌内分泌治疗的基本原则和新动向——2006年美国NCCN乳癌内分泌治疗指南解读[J].临床药物治疗杂志,2006,4(2):21-25. 被引量:20
  • 2张瑰红,施达仁,梁晓曼,侯景辉,康苏娅,朱卫东,李晓兵,邵云,陈丽荣,周燕.显色原位杂交和免疫组织化学检测乳腺癌HER2/neu基因状况和蛋白表达的对照性研究[J].中华病理学杂志,2006,35(10):580-583. 被引量:29
  • 3<乳腺癌HER2检测指南>编写组,霍临明.乳腺癌HER2检测指南[J].中华病理学杂志,2006,35(10):631-633. 被引量:165
  • 4Goldhirsch A, Wood WC, Coates AS,et al. Strategies for sub- types-dealing with the diversity of breast cancer: highlights of the St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2011 [J].Ann Oncol,2011,22(8): 1736-1747.
  • 5Goldhirsch A, Wood WC, Gelher RD, et al. Progress and prom- ise: highlights of the international expert consensus on the pri- mary therapy of early breast cancer 2007 [ J ] . Ann Oncol, 2007, 18(7):1133-1144.
  • 6Goldhirsch A, Ingle JN, Gelber RD, et al. Thresholds for thera- pies: highlights of the St Gallen International Expert Consensus on the primary therapy of early breast cancer 2009 [J ].Ann On- col, 2009,20(8): 1319-1329.
  • 7Carey LA, Perou CM, Livasy CA, et al. Race, Breast cancer subtypes and survival in the Carolina breast cancer study [J]. JAMA, 2006,295(21) : 2492-2502.
  • 8Phipps AI, Chlebowski RT, Prentice R, et al. Body size, physical activity, and risk of triple-negative and estrogen receptor-posi- tive breast cancer[J]. Cancer Epidemiol Biomarkers Prey,2011 , 20(3):454-463.
  • 9Phipps AI, Buist DS, Malone KE, et al. Reproductive history and risk of three breast cancer subtypes defined by three biomarkers [J]. Cancer Causes Control, 2011,22(3):399-405.
  • 10Albain KS, Barlow WE, Shak S,et al. Breast Cancer Intergroup of North America. Prognostic and predictive value of the 21-gene recurrence score assay in postmenopausal women with node-positive, oestrogen-receptor-positive breast cancer on chemotherapy: a retrospective analysis of a randomised trial [J]. Lancet Oncol,2010,11(1):55-65.

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