Department of Pathology, Faculty of Medicine, University of Ruhuna, Galle, 80000, Sri Lanka.
Medical Laboratory Science Degree Programme, Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka.
BMC Cancer. 2018 May 24;18(1):589. doi: 10.1186/s12885-018-4491-6.
This study was carried out to evaluate the prognostic value of KIBRA in breast cancer.
This retrospective study included breast cancer patients who sought the services of the immunohistochemistry laboratory of our unit from 2006 to 2015. Tissue microarrays were constructed and immunohistochemical staining was done to assess the KIBRA expression. The Kaplan-Meier model for univariate and Cox-regression model with backward stepwise factor retention method for multivariate analyses were used. Chi square test was used to find out the associations with the established prognostic features.
A total of 1124 patients were included in the study and KIBRA staining of 909 breast cancers were available for analysis. Cytoplasmic KIBRA expression was seen in 39.5% and nuclear expression in 44.8%. Overall KIBRA-low breast cancers accounted for 41.5%. KIBRA nuclear expression was significantly associated with positive ER and PR expression. Luminal breast cancer patients who had endocrine therapy and KIBRA-low expression had a RFS disadvantage over those who were positive for KIBRA (p = 0.02). Similarly, patients who received chemotherapy and had overall KIBRA-low expression also demonstrated a RFS disadvantage compared to those who had overall positive KIBRA expression (p = 0.018). This effect of KIBRA was independent of the other factors considered for the model.
Overall low-KIBRA expression has an independent effect on the RFS and predicts the RFS outcome of luminal breast cancer patients who received endocrine therapy and breast cancer patients who received chemotherapy.
本研究旨在评估 KIBRA 在乳腺癌中的预后价值。
本回顾性研究纳入了 2006 年至 2015 年期间在我院免疫组化实验室就诊的乳腺癌患者。构建组织微阵列并进行免疫组织化学染色,以评估 KIBRA 表达。采用单因素 Kaplan-Meier 模型和多因素 Cox 回归模型逐步后退法进行分析。采用卡方检验确定与既定预后特征的关联。
共纳入 1124 例患者,其中 909 例乳腺癌的 KIBRA 染色结果可供分析。细胞质 KIBRA 表达见于 39.5%的病例,核表达见于 44.8%的病例。总体而言,KIBRA 低表达的乳腺癌占 41.5%。KIBRA 核表达与 ER 和 PR 阳性表达显著相关。接受内分泌治疗且 KIBRA 低表达的 luminal 型乳腺癌患者的 RFS 劣于 KIBRA 阳性患者(p=0.02)。同样,接受化疗且总体 KIBRA 低表达的患者与总体 KIBRA 阳性表达的患者相比,RFS 也较差(p=0.018)。KIBRA 的这种作用独立于模型中考虑的其他因素。
总体上 KIBRA 低表达对 RFS 有独立影响,并预测接受内分泌治疗的 luminal 型乳腺癌患者和接受化疗的乳腺癌患者的 RFS 结局。