期刊文献+

原发性乳腺癌AS160分子磷酸化水平与肿瘤细胞增殖活性指标的相关性分析 被引量:1

Correlation of AS160 phosphorylation with tumor cell proliferative activity in primary breast cancer
下载PDF
导出
摘要 目的探讨乳腺癌组织中磷酸化AS160(Thr642)水平上调与肿瘤细胞增殖活性指标之间的关系。方法回顾性分析中国人民解放军第八五医院2003年1月至2015年1月收治的152例乳腺癌患者的临床病理资料。采用免疫组织化学方法检测肿瘤组织中磷酸化AS160(Thr642)及增殖指标Ki-67(MIB-1)水平,对肿瘤组织作核分裂象计数,并观察乳腺癌细胞株MDA-MB-231中磷酸化AS160(Thr642)的表达特点。采用Spearman检验分析磷酸化AS160(Thr642)与核分裂象计数、Ki-67(MIB-1)的相关性。结果磷酸化AS160(Thr642)与核分裂象计数、Ki-67(MIB-1)呈显著正相关(r=0.493、0.472,P均<0.001)。乳腺癌组织与细胞株中的有丝分裂象细胞磷酸化AS160(Thr642)呈强阳性。结论磷酸化AS160分子的表达能反映乳腺癌细胞的增殖活性,是乳腺癌的1个有价值的标志物和治疗靶分子。 Objective To investigate the correlation of phosphorylation AS160(Thr642) regulation with tumor cell proliferative activity in breast cancer tissue. Methods The clinical data of 152 patients with breast cancer in 85 Hospital of People's Liberation Army from January 2003 to January 2015 were analyzed retrospectively. Immunohistochemical method was used to determine phosphorylation AS160(Thr642) and proliferation Ki-67(MIB-1) levels. Mitotic index was evaluated,and the expression characteristics of phosphorylation AS160(Thr642)was investigated in breast cancer cell line MDA-MB-231. The correlations of phosphorylation AS160(Thr642) with mitotic index and Ki-67(MIB-1) were analyzed by Spearman nonparametric test. Results The phosphorylation AS160(Thr642) was positively correlated with mitotic index(r=0.493,P〈0.001) and Ki-67(MIB-1)(r=0.472,P〈0.001). The phosphorylation AS160(Thr642) in mitotic tumor cells was strongly positive in cell line and breast cancer tissue. Conclusions The phosphorylation AS160 is correlated with tumor cell proliferative activity and might be useful as a marker and a potential treatment target for breast cancer.
出处 《检验医学》 CAS 2016年第3期220-223,共4页 Laboratory Medicine
基金 南京军区医学科技创新课题(12Z02)
关键词 AS160 乳腺肿瘤 磷酸化 细胞增殖 AS160 Breast cancer Phosphorylation Cell proliferation
  • 相关文献

参考文献3

二级参考文献14

  • 1沈丹华,张雅贤.中间滋养细胞肿瘤及瘤样病变[J].中华病理学杂志,2004,33(5):481-483. 被引量:14
  • 2Hong-LingLi,Bing-ZhongSun,Fu-ChengMa.Expression of COX-2,iNOS,p53 and Ki-67 in gastric mucosa-associated lymphoid tissue lymphoma[J].World Journal of Gastroenterology,2004,10(13):1862-1866. 被引量:21
  • 3姜小华,狄杨,蒋晓飞,孙建文,傅德良,刘春芳,吕元.从睾丸cDNA表达文库筛选胰腺癌肿瘤抗原[J].中华检验医学杂志,2007,30(7):750-752. 被引量:3
  • 4Kane S, Sano H, Liu SC, et al. A method to identify serine kinase substrates Akt phosphorylates a novel adipocyte protein with a Rab GTPase-activating protein (GAP) domain [ J ]. J Biol Chem ,2002,277 (25) :22115-22118.
  • 5Jiang XH,Sun JW,Xu M,et al. Frequent hyperphosphorylation of AS160 in breast cancer [ J]. Cancer Biol Ther, 2010, 10(4) :362-367.
  • 6Tsutsui S, Ohno S, Murakami S, et al. Prognostic value of c-erbB-2 expression in breast cancer[ J ]. J Surg Oncol,2002, 79(4) :216-223.
  • 7Capala J, Bouchelouche K. Molecular imaging of HER2-positive breast cancer: a step toward an individualized 'image and treat' strategy[Jl. Curt Opin Oncol,2010,22(6) :559-566.
  • 8Sakamoto K, Holman GD. Emerging role for AS160/TBC1D4 and TBC1D1 in the regulation of GLUT4 traffic[J]. J Am Physiol Endocrinol Metab ,2008,295 ( 1 ) : E29-E37.
  • 9Bartlett JM. Biomarkers and patient selection for PI3K/Akt/ mTOR targeted therapies: current status and future directions [ J]. Clin Breast Cancer, 2010,10 ( Suppl 3 ) : S86-S95.
  • 10Salh B, Marotta A, Wagey R, et al. Dysregulation of phosphatidylinositol 3-kinase and downstream effectors in human breast cancer[ J]. Int J Cancer, 2002,98 (1) : 148-154.

共引文献53

同被引文献17

引证文献1

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