Kleer Celina G, Griffith Kent A, Sabel Michael S, Gallagher Gary, van Golen Kenneth L, Wu Zhi-Fen, Merajver Sofia D
Department of Pathology and Internal Medicine, University of Michigan, Ann Arbour, MI 48109-0054, USA.
Breast Cancer Res Treat. 2005 Sep;93(2):101-10. doi: 10.1007/s10549-005-4170-6.
There is a need for reliable predictors of breast cancer aggressiveness that will further refine the staging classification and help guide the implementation of novel therapies. We have identified RhoC as being nearly always overexpressed in the most aggressive form of breast cancer, inflammatory breast cancer (IBC); in subsequent work we identified RhoC to be a promising marker of aggressive behavior in breast cancers less than 1 cm in diameter. We hypothesized that RhoC expression would identify aggressive, non-IBC tumors breast cancer patients at any stage with worse outcomes defined as recurrence and/or metastasis.
We constructed four high-density tissue microarrays (TMAs) using 801 tissue cores from 280 patients. These tissues represent a wide range of normal breast and breast disease, including intraductal hyperplasia, ductal carcinoma in situ (DCIS), invasive carcinomas, and distant metastases. The TMAs were immunostained using a polyclonal anti-RhoC antibody developed in our laboratory. Cytoplasmic RhoC expression was scored as negative, weak, moderate, or strong by a previously validated scoring schema.
RhoC expression increases with breast cancer progression. All samples of normal breast epithelium had negative to weak staining, whereas staining intensity increased in hyperplasia, DCIS, invasive carcinoma, and metastases (Kruskal-Wallis p < 0.001). In patients with invasive carcinoma, high RhoC expression was associated with features of aggressive behavior including high histologic grade, positive lymph nodes, and negative hormonal receptor status. High RhoC expression was a predictor of overall survival in patients with breast cancer (log rank test, p = 0.002) and was associated with 100% increase in the risk of death as compared to patients with low RhoC expression. Importantly, high RhoC was an independent predictor of poor response to doxorubicin-based chemotherapy with a hazard ratio of 3.1 and a 95% CI of 1.2-7.7 (p = 0.02).
RhoC expression increases with breast cancer progression and RhoC protein level in tumor tissue is strongly associated with biologically aggressive invasive carcinomas of the breast. RhoC expression, if validated, may identify patients who are less likely benefit from doxorubicin therapy and suggests RhoC overexpression as a new target for intervention.
需要可靠的乳腺癌侵袭性预测指标,以进一步完善分期分类并指导新疗法的实施。我们已确定RhoC在最具侵袭性的乳腺癌——炎性乳腺癌(IBC)中几乎总是过度表达;在后续研究中,我们发现RhoC是直径小于1厘米的乳腺癌侵袭性行为的一个有前景的标志物。我们假设RhoC表达可识别任何阶段具有侵袭性的非IBC肿瘤乳腺癌患者,其预后较差,定义为复发和/或转移。
我们使用来自280名患者的801个组织芯构建了四个高密度组织微阵列(TMA)。这些组织代表了广泛的正常乳腺和乳腺疾病,包括导管内增生、原位导管癌(DCIS)、浸润性癌和远处转移。使用我们实验室开发的多克隆抗RhoC抗体对TMA进行免疫染色。根据先前验证的评分方案,将细胞质RhoC表达评分为阴性、弱阳性、中等或强阳性。
RhoC表达随乳腺癌进展而增加。所有正常乳腺上皮样本的染色均为阴性至弱阳性,而增生、DCIS、浸润性癌和转移灶中的染色强度增加(Kruskal-Wallis检验,p<0.001)。在浸润性癌患者中,高RhoC表达与侵袭性行为特征相关,包括高组织学分级、阳性淋巴结和阴性激素受体状态。高RhoC表达是乳腺癌患者总生存的一个预测指标(对数秩检验,p = 0.002),与低RhoC表达患者相比,死亡风险增加100%。重要的是,高RhoC是基于阿霉素化疗反应不佳的独立预测指标,风险比为3.1,95%CI为1.2 - 7.7(p = 0.02)。
RhoC表达随乳腺癌进展而增加,肿瘤组织中的RhoC蛋白水平与乳腺具有生物学侵袭性的浸润性癌密切相关。如果得到验证,RhoC表达可能识别出不太可能从阿霉素治疗中获益的患者,并提示RhoC过表达作为一个新的干预靶点。