Zhou Su-juan, Guo Hua
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Zhonghua Yi Xue Za Zhi. 2013 Sep 24;93(36):2895-7.
To analyze Ki-67 expression and explore its significance in different molecular subtypes of breast invasive ductal carcinoma (IDC).
The expressions of estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor-2 (HER-2) and Ki-67 were detected in 126 cases of IDC by immunohistochemical staining. Then the molecular subtype of each case of IDC was determined.Statistical analysis was performed to determine the relationship between Ki-67 expression and the molecular subtypes with clinicopathological features of IDC.
There was no statistically significant difference of Ki-67 expression in age and tumor size (P > 0.05).However, significant difference existed in histological grading and lymph node metastasis (P < 0.05). The expression level of Ki-67 was negatively correlated with ER expression (r = -0.273, P = 0.002) and PR expression (r = -0.242, P = 0.007) and positively with HER-2 expression (r = 0.245, P = 0.006) . A low expression of Ki-67 was in LumianlA subtype (17/17) and high expression in other molecular subtypes. Moreover, the rate of high expression (Ki-67 LI>50%) in each subtype progressively increased with the degree of molecular typing and Ki-67 expression in different molecular subtypes showed significant difference (P < 0.05).
The expression level of Ki-67 is correlated with histological grading and molecular type of IDC. High expression of Ki-67 carries poor prognosis. Thus it is necessary to perform a variety of routine clinicopathological examinations, such as Ki-67, ER, PR and HER-2.
分析Ki-67在乳腺浸润性导管癌(IDC)不同分子亚型中的表达情况并探讨其意义。
采用免疫组织化学染色法检测126例IDC患者雌激素受体(ER)、孕激素受体(PR)、人表皮生长因子受体2(HER-2)及Ki-67的表达,确定各例IDC的分子亚型,并进行统计学分析,以确定Ki-67表达与IDC分子亚型及临床病理特征之间的关系。
Ki-67表达在年龄和肿瘤大小方面无统计学差异(P>0.05),但在组织学分级和淋巴结转移方面存在显著差异(P<0.05)。Ki-67表达水平与ER表达呈负相关(r=-0.273,P=0.002),与PR表达呈负相关(r=-0.242,P=0.007),与HER-2表达呈正相关(r=0.245,P=0.006)。Ki-67在LumianlA亚型中低表达(17/17),在其他分子亚型中高表达。此外,各亚型中高表达率(Ki-67 LI>50%)随分子分型程度逐渐升高,不同分子亚型的Ki-67表达存在显著差异(P<0.05)。
Ki-67表达水平与IDC的组织学分级和分子类型相关,Ki-67高表达预后较差。因此,有必要进行多种常规临床病理检查,如检测Ki-67、ER、PR及HER-2。