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首页> 外文期刊>International Journal of Clinical and Experimental Medicine >Associations between clinicopathological prognostic factors and pAkt, pMAPK and topoisomerase II expression in breast cancer
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Associations between clinicopathological prognostic factors and pAkt, pMAPK and topoisomerase II expression in breast cancer

机译:临床病理预后因素与乳腺癌中pAkt,pMAPK和拓扑异构酶II表达的关系

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This study aimed to examine the associations between mitogen activated protein kinase (MAPK), Akt, and topoisomerase II expression and other well established clinical and pathological prognostic factors in patients with breast cancer. A total of 42 women with breast cancer who underwent anthracycline based chemotherapy were included in this retrospective study. Immunohistochemical methods were utilized to examine the expression of phosphorylated MAPK (pMAPK), phosphorylated Akt (pAkt), HER-2/emneu/em and topoisomerase IIα (topo IIα) in tissue blocks. Subsequently, the associations between pMAPK, pAkt, and topoisomerase IIα (topo IIα) expression characteristics and disease stage (T and N), tumor grade, estrogen/progesteron receptor status, and HER-2/emneu/em expression were explored. Median age of the patients was 63 years (range, 37-82). There was a significant association between N stage and topoisomerase IIα expression (emP/em = 0.021), with increasing rates of positivity in higher grades: N0, 22.7%; N1, 11.1%; N2, 42.9%; N3, 100%. In addition, topo IIα expression was higher in estrogen receptor-positive versus estrogen receptor-negative tumors (50% vs. 0%, emP/em = 0.0004) and MAPK expression was more frequent among progesteron receptor-positive versus negative tumors (64.0 versus 20.0%, emP/em = 0.027). Our results show that the tissue expression of topo IIα and MAPK, which play a role in the intracellular signal pathways, is associated with certain established prognostic factors in breast cancer. Further studies examining survival rates and involving larger sample populations are warranted to better define the importance of the observed associations.
机译:这项研究的目的是检查有丝分裂原活化蛋白激酶(MAPK),Akt和拓扑异构酶II表达与乳腺癌患者其他公认的临床和病理预后因素之间的关联。这项回顾性研究包括总共42例接受蒽环类化疗的乳腺癌女性。免疫组织化学方法检测磷酸化的MAPK(pMAPK),磷酸化的Akt(pAkt),HER-2 / neu 和拓扑异构酶II&#x003b1的表达。 (topo IIα)组织块中。随后,pMAPK,pAkt和拓扑异构酶II&#x003b1之间的关联; (topo IIα)表达特征和疾病阶段(T和N),肿瘤等级,雌激素/黄体酮受体状态和HER-2 / neu 表达进行了探讨。患者的中位年龄为63岁(范围37-82)。 N期与拓扑异构酶II&#x003b1之间存在显着关联。表达( P = 0.021),随着年级的提高,阳性率增加:N0,22.7%; N1,11.1%; N2,42.9%; N3,100%。另外,topo IIα雌激素受体阳性肿瘤的表达高于雌激素受体阴性肿瘤(50%vs. 0%, P = 0.0004),而孕激素受体阳性肿瘤与阴性肿瘤中MAPK表达更为频繁(64.0 vs. 20.0%, P = 0.027)。我们的结果表明topo IIα的组织表达。 MAPK和MAPK在细胞内信号通路中起作用,与某些确定的乳腺癌预后因素有关。为了确保更好地确定所观察到的关联的重要性,有必要进行进一步研究,以研究存活率并涉及更多的样本人群。

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