Wu Yanyuan, Mohamed Hezla, Chillar Ram, Ali Ishrat, Clayton Sheila, Slamon Dennis, Vadgama Jaydutt V
Divisions of Cancer Research and Training, Hematology/Oncology, Department of Medicine, Charles R. Drew University of Medicine and Science, 1731 East 120th Street, Los Angeles, CA 90059, USA.
Breast Cancer Res. 2008;10(1):R3. doi: 10.1186/bcr1844. Epub 2008 Jan 10.
Breast cancer patients with HER2/neu overexpression have poor outcomes with a decrease in disease-free survival (DFS) and overall survival. The biology of HER2/neu overexpression in breast tumors in African-American and Latina women is poorly understood. The purpose of this study is to understand the clinical significance of activated Akt (phospho-Akt or pAkt) expression in breast tumors from African-American and Latina patients with corresponding tissue HER2/neu overexpression. Cellular and molecular studies have shown that activation of the cell signaling phosphatidylinositol-3-kinase/Akt cascade via the HER2/neu and other receptor tyrosine kinases induces cell proliferation.
A total of 234 African-American and Latina patients were selected retrospectively. From this group, 141 tumor tissue samples were analyzed for tissue pAkt by immunohistochemistry (IHC). This cohort consisted of 46 HER2/neu-positive (3+ by IHC) and 95 HER2/neu-negative tumors. The prognostic value of activated tissue Akt in relation to HER2/neu overexpression for DFS was determined.
Patients with low pAkt and HER2-negative tumors had the best DFS. As expected, HER2/neu-overexpressing tumors with low pAkt had a decrease in DFS. Similarly, those with high pAkt and HER2-negative tumors also had poor DFS. However, those with an increase in both HER2 and pAkt had the worst DFS. An increase in pAkt was significantly associated with HER2/neu-positive and lymph node-positive breast tumors. Tumors with high HER2 and high pAkt were metastatic. Multivariate analysis demonstrated that, in addition to the common risk factors such as larger tumor size, lymph node involvement, estrogen receptor/progesterone receptor-negative tumors, and HER2/neu-positive tumors, overexpression of pAkt significantly was associated with a decrease in 5-year DFS. A decrease in DFS with an increase in pAkt was observed in both HER2/neu-positive and -negative groups. However, the DFS was similar between HER2/neu-positive/pAkt-negative and HER2/neu-negative/pAkt-positive groups.
Our data suggest that there may be differences in tumor phenotypes within the HER2/neu-overexpressing breast cancer patients. The overexpression of pAkt may be a powerful prognostic marker for predicting DFS and overall survival of breast cancer patients.
HER2/neu过表达的乳腺癌患者预后较差,无病生存期(DFS)和总生存期均缩短。非洲裔美国女性和拉丁裔女性乳腺肿瘤中HER2/neu过表达的生物学机制尚不清楚。本研究旨在了解非洲裔美国和拉丁裔HER2/neu相应组织过表达患者乳腺肿瘤中活化Akt(磷酸化Akt或pAkt)表达的临床意义。细胞和分子研究表明,通过HER2/neu和其他受体酪氨酸激酶激活细胞信号磷脂酰肌醇-3-激酶/Akt级联可诱导细胞增殖。
回顾性选取234例非洲裔美国和拉丁裔患者。从该组中,选取141例肿瘤组织样本通过免疫组织化学(IHC)分析组织pAkt。该队列包括46例HER2/neu阳性(IHC 3+)和95例HER2/neu阴性肿瘤。确定活化组织Akt相对于HER2/neu过表达对DFS的预后价值。
pAkt低且HER2阴性肿瘤的患者DFS最佳。正如预期的那样,pAkt低的HER2/neu过表达肿瘤的DFS降低。同样,pAkt高且HER2阴性肿瘤的患者DFS也较差。然而,HER2和pAkt均升高的患者DFS最差。pAkt升高与HER2/neu阳性和淋巴结阳性乳腺肿瘤显著相关。HER2高且pAkt高的肿瘤发生转移。多变量分析表明,除了肿瘤较大、淋巴结受累、雌激素受体/孕激素受体阴性肿瘤和HER2/neu阳性肿瘤等常见危险因素外,pAkt过表达与5年DFS降低显著相关。在HER2/neu阳性和阴性组中均观察到DFS随pAkt升高而降低。然而,HER2/neu阳性/pAkt阴性组和HER2/neu阴性/pAkt阳性组之间的DFS相似。
我们的数据表明,HER2/neu过表达的乳腺癌患者的肿瘤表型可能存在差异。pAkt过表达可能是预测乳腺癌患者DFS和总生存期的有力预后标志物。