期刊文献+

三阴性乳腺癌中程序性死亡配体1的表达及其与PTEN基因的关系 被引量:4

Expression of programmed death ligand 1 in triple negative breast cancer and its relationship with PTEN
原文传递
导出
摘要 目的探讨程序性死亡配体1(PD-L1)在三阴性乳腺癌(TNBC)中的表达情况及其与PTEN基因的关系。方法通过癌症基因组图谱(TCGA)数据库查询PD-L1 mRNA在浸润性乳腺癌数据集(包括115例TNBC和702例非TNBC)中的表达情况。收集2012年1月至2016年12月解放军第180医院收治的182例浸润性乳腺癌术后石蜡包埋组织标本,包括62例TNBC和120例非TNBC,并用免疫组织化学方法检测PD-L1和PTEN的表达情况。用t检验比较TCGA数据库中2组的PD-L1 mRNA表达量,率的比较用χ~2检验,Mann-Whitney U秩和检验比较石蜡标本中2组PD-L1表达强度,并用χ2检验和Spearman秩相关检验分析PD-L1与PTEN表达的相关性。结果 TCGA数据库分析显示,浸润性乳腺癌中3. 8%(31/817)有PD-L1 mRNA上调,其中TNBC组的表达上调率为8. 7%(10/115),高于非TNBC组的3. 0%(21/702)(χ~2=7. 314,P=0. 007),TNBC组的PD-L1 mRNA表达量为8. 05±0. 91,高于非TNBC组的7. 38±0. 73 (t=7. 510,P<0. 001)。石蜡标本的免疫组织化学结果显示,TNBC组的PDL1阳性表达率为14. 5%(9/62),高于非TNBC组的5. 0%(6/120)(χ~2=4. 895,P=0. 027),而且PD-L1阳性表达强度也高于非TNBC组(Z=-2. 291,P=0. 022)。TNBC石蜡标本中PD-L1与PTEN蛋白表达呈负相关(χ~2=6. 913,P=0. 009; r=-0. 382,P=0. 002)。结论 TNBC中PD-L1表达高于非TNBC,并与PTEN负相关,其可能成为TNBC患者的免疫治疗靶点。 ObjectiveTo investigate the expression of programmed death ligand 1(PD-L1) in triple negative breast cancer (TNBC) and its relationship with PTEN expression.Methods In the Cancer Genome Atlas (TCGA) database, the expression of PD-L1 mRNA in the invasive breast cancer dataset was analyzed, including 115 TNBC cases and 702 non-TNBC cases. A total of 182 paraffin-embedded tissue specimens from invasive breast cancer patients admitted to the No.180 Hospital of PLA from January 2012 to December 2016 were collected and the expression of PD-L1 and PTEN was immunohistochemically detected. PD-L1 mRNA expression was compared between two groups in TCGA database using t test.χ 2 test was used to compare the rates.The intensity of PD-L1 positive expression in paraffin-embedded specimens were compared between two groups using Mann-Whitney U test. χ 2 test and Spearman rank test were used to analyze the correlation between PD-L1 and PTEN expression.Results In TCGA database, PD-L1 mRNA level was up-regulated in 3.8% (31/817) of invasive breast cancer. The up-regulation rate of PD-L1 mRNA in TNBC (8.7%,10/115) was significantly higher than that in non-TNBC (3.0%,21/702) (χ 2=7.314, P =0.007). PD-L1 mRNA expression in TNBC was significantly higher than that in non-TNBC(8.05±0.91 vs 7.38±0.73, t =7.510, P 〈0.001). The immunohistological results of 182 paraffin-embedded tissue specimens showed that the positive expression rate of PD-L1 in TNBC (14.5%,9/62) was significantly higher than that in non-TNBC(5.0%, 6/120 )(χ 2=4.895, P =0.027), and the expression intensity of PD-L1 in TNBC was significantly higher than that in non-TNBC( Z =-2.291, P =0.022). The PD-L1 protein expression was negatively correlated with PTEN protein expression in paraffin-embedded TNBC specimens (χ 2=6.913, P = 0.009, r =-0.382, P =0.002).Conclusion PD-L1, which shows higher expression in TNBC patients than in non-TNBC patients and a negative correlation with PTEN, may be a potential target for TNBC
作者 魏开鹏 陈海莺 陈燕红 邱建龙 Wei Kaipeng;Chen Haiying;Chen Yanhong;Qiu Jianlong(Department of Pathology,2Department of Surgery,No.180 Hospital of PLA,Quanzhou 362000,China)
机构地区 解放军第 解放军第
出处 《中华乳腺病杂志(电子版)》 CAS CSCD 2018年第5期294-298,共5页 Chinese Journal of Breast Disease(Electronic Edition)
关键词 乳腺肿瘤 免疫组织化学 PTEN磷酸水解酶 Breast neoplasms Immunohistochemistry PTEN phosphohydrolase
  • 相关文献

参考文献3

二级参考文献21

  • 1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
  • 2<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
  • 3Harris L, Fritsche H, Mennel R, et al. American Society of Clinical Oncology 2007 update of recommendations for the use of tumor markers in breast cancer [ J]. J Clin Oncol, 2007, 25 (33) :5287-5312. 被引量:1
  • 4Wolff AC, Hammond ME, Schwartz JN, et al. American Society of Chnical Oncology/College of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer[ Jl. J Clin Oncol, 2007, 25 ( 1 ) : 118- 145. 被引量:1
  • 5Wolff AC, Hammond ME, Hicks DG, et al. Recommendations for human epidermal growth faetor reeeptor 2 testing in breast eaneer: American Society of Clinical Oneology/College of American Pathologists clinical practice guideline update[J]. J Clin Oneol, 2013, 31 (31) :3997-4013. 被引量:1
  • 6Hanna WM, Kwok K. Chromogenic in-situ hybridization:a viable ahernative to fluorescence in-situ hybridization in the HER2 testing algorithm[J]. Mod Pathol, 2006, 19(4) :481-487. 被引量:1
  • 7Park K, Han S, Kim JY, et al. Silver-enhanced in situ hybridization as an alternative to fluorescence in situ hybridization for assaying HER2 amplification in clinical breast cancer [ J ]. J Breast Cancer, 2011, 14(4) :276-282. 被引量:1
  • 8Haines GK 3rd, Wiley E, Susnik B, et al. HER2 in well differentiated breast cancer: is testing necessary? [ J ]. Breast Cancer Res Treat, 2008, 112(3) :551-556. 被引量:1
  • 9Zhu X, Lu Y, Lu H, et al. Genetic alterations and protein expression of HER2 and chromosome 17 polysomy in breast cancer [J]. Hum Pathol, 2011,42(10) : 1499-1504. 被引量:1
  • 10Marchio C, Lambros MB, Gugliotta P, et al. Does chromosome 17 centromere copy number predict polysomy in breast cancer.9 A fluorescence in situ hybridization and microarray-based CGH analysis[ J]. J Pathol, 2009, 219( 1 ) : 16-24. 被引量:1

共引文献322

同被引文献42

引证文献4

二级引证文献20

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