Tawab Osman Nisreen, Khalaf Manal, Ibraheem Shaymaa
Pathology Department, Faculty of Medicine, Minia University, Egypt.
Pol J Pathol. 2020;71(2):87-98. doi: 10.5114/pjp.2020.97016.
Breast cancer is the most leading cause of cancer death in females worldwide. Identification of novel biomarkers for prognosis is required. Imunohistochemical evaluation of CIP2A and ROCK-1 expressions in 126 breast tissue specimens stratified as 21 ductal hyperplasias, 17 duct carcinoma in situ (DCIS) and 88 invasive carcinomas (56 invasive ductal carcinomas NST, 32 invasive lobular carcinomas) was studied. High CIP2A expression was detected in 48.9% of invasive carcinomas. CIP2A overexpression was significantly related to Nottingham prognostic index (NPI) (p = 0.011), stage (p = 0.01), ER negativity (p = 0.031), PR negativity (p = 0.048), and HER-2 positivity (p = 0.02). CIP2A was significantly overexpressed in triple-negative breast cancer (TNBC) (p = 0.004). ROCK-1 expression was detected in 54.5% of invasive carcinomas. Statistically significant associations were observed between ROCK-1 expression and NPI (p = 0.032), stage (p = 0.002), ER negativity (p = 0.012), PR negativity (p = 0.023), HER-2 positivity (p = 0.016), and TNBC subtype (p = 0.033). A positive association between CIP2A and ROCK-1 expressions (p < 0.0001) was documented. There was a significant association between shorter overall survival and high CIP2A and positive ROCK-1 expressions (p < 0.0001) and (p < 0.0001). CIP2A and ROCK-1 expressions could be used as markers for the poor prognosis of breast cancer.
乳腺癌是全球女性癌症死亡的首要原因。需要鉴定新的预后生物标志物。本研究对126份乳腺组织标本进行了CIP2A和ROCK-1表达的免疫组化评估,这些标本分为21例导管增生、17例原位导管癌(DCIS)和88例浸润性癌(56例浸润性导管癌非特殊型、32例浸润性小叶癌)。在48.9%的浸润性癌中检测到CIP2A高表达。CIP2A过表达与诺丁汉预后指数(NPI)(p = 0.011)、分期(p = 0.01)、雌激素受体阴性(p = 0.031)、孕激素受体阴性(p = 0.048)和HER-2阳性(p = 0.02)显著相关。CIP2A在三阴性乳腺癌(TNBC)中显著过表达(p = 0.004)。在54.5%的浸润性癌中检测到ROCK-1表达。观察到ROCK-1表达与NPI(p = 0.032)、分期(p = 0.002)、雌激素受体阴性(p = 0.012)、孕激素受体阴性(p = 0.023)、HER-2阳性(p = 0.016)和TNBC亚型(p = 0.033)之间存在统计学显著关联。记录到CIP2A和ROCK-1表达之间存在正相关(p < 0.0001)。总生存期较短与CIP2A高表达和ROCK-1阳性表达之间存在显著关联(p < 0.0001)和(p < 0.0001)。CIP2A和ROCK-1表达可作为乳腺癌预后不良的标志物。