Jiang You-Hua, Cheng Bo, Ge Ming-Hua, Zhang Gu
Department of Thoracic Surgery, Zhejiang Cancer Hospital, and The Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310022, China.
Head Neck Oncol. 2012 Mar 27;4:9. doi: 10.1186/1758-3284-4-9.
Myoepithelial carcinoma is a rare tumour. The clinical and biological behaviours of these tumours are variable. Although many factors have been evaluated as potential prognostic indicators, including clinical stage, site and size of the tumour, high proliferative activity, extensive invasion into the surrounding tissue, perineural permeation, the abnormal presence of nuclear DNA content, and marked cellular pleomorphism, there are no definite histological features that clearly correlate with their behaviour. Thus, conclusions regarding prognostic factors and ideal treatment may emerge as the number of investigated myoepithelial carcinoma cases accumulate.
Using immunohistochemistry, expression levels of p63 and Ki-67 were determined in 16 myoepithelial carcinoma samples and correlated with clinicopathological characteristics and patient prognosis.
p63 expression was detected in six of the myoepithelial carcinoma tissues (37.5%) and Ki-67 was detected in five (31.3%). In addition, p63 and Ki-67 expression levels were associated with myoepithelial carcinoma recurrence and metastasis. All six patients with p63-positive expression died due to disease or cardiovascular disease (mean survival time = 50.5 months), and p63 expression was statistically significant with respect to survival (P = 0.01). Four patients with Ki-67-positive expression died due to disease or cardiovascular disease (mean survival time = 44.0 months); however, there was no statistically significant difference between Ki-67 expression and survival (P = 0.24).
Recurrence and metastasis in myoepithelial carcinomas are more frequent in p63-positive and Ki-67-positive EMCs, and poor prognosis is associated with overexpression of p63.
肌上皮癌是一种罕见肿瘤。这些肿瘤的临床和生物学行为具有多样性。尽管许多因素已被评估为潜在的预后指标,包括临床分期、肿瘤部位和大小、高增殖活性、广泛侵犯周围组织、神经周围浸润、核DNA含量异常以及明显的细胞多形性,但尚无明确的组织学特征能清晰地与其行为相关联。因此,随着所研究的肌上皮癌病例数量的积累,关于预后因素和理想治疗的结论可能会出现。
采用免疫组织化学方法,测定16例肌上皮癌样本中p63和Ki-67的表达水平,并将其与临床病理特征及患者预后相关联。
在16例肌上皮癌组织中,6例检测到p63表达(37.5%),5例检测到Ki-67表达(31.3%)。此外,p63和Ki-67的表达水平与肌上皮癌的复发和转移相关。所有6例p63阳性表达患者均死于疾病或心血管疾病(平均生存时间=50.5个月),p63表达在生存方面具有统计学意义(P=0.01)。4例Ki-67阳性表达患者死于疾病或心血管疾病(平均生存时间=44.0个月);然而,Ki-67表达与生存之间无统计学显著差异(P=0.24)。
p63阳性和Ki-67阳性的肌上皮癌复发和转移更为频繁,p63过表达与预后不良相关。