Nicholson R I, McClelland R A, Gee J M, Manning D L, Cannon P, Robertson J F, Ellis I O, Blamey R W
Breast Cancer Laboratory, Tenovus Cancer Research Centre, Cardiff, United Kingdom.
Cancer Res. 1994 Apr 1;54(7):1684-9.
The expression of transforming growth factor-alpha (TGF-alpha) has been evaluated in 51 breast cancers of known responsiveness to endocrine therapy using immunohistochemistry. High levels of TGF-alpha were observed in 65% of tumors and showed no relationship with tumor estrogen receptor or epidermal growth factor receptor status or Ki67 immunostaining. TGF-alpha levels did, however, relate to the endocrine sensitivity of the disease, with unresponsive tumors frequently showing high levels of TGF-alpha immunoreactivity. This relationship was observed in estrogen receptor-positive disease and was independent of the epidermal growth factor receptor status of the tumor. No quantitative association between TGF-alpha and Ki67 immunostaining was observed in any of the subcategories of tumors. These data infer a role for TGF-alpha in the development of endocrine insensitivity in estrogen receptor-positive breast cancer by mechanisms which appear independent of tumor growth fraction, as determined by Ki67 immunostaining.
利用免疫组织化学方法,对51例已知内分泌治疗反应性的乳腺癌中转化生长因子-α(TGF-α)的表达情况进行了评估。在65%的肿瘤中观察到高水平的TGF-α,且其与肿瘤雌激素受体、表皮生长因子受体状态或Ki67免疫染色均无关联。然而,TGF-α水平确实与疾病的内分泌敏感性相关,无反应性肿瘤常常表现出高水平的TGF-α免疫反应性。在雌激素受体阳性疾病中观察到了这种关系,且与肿瘤的表皮生长因子受体状态无关。在任何肿瘤亚类中均未观察到TGF-α与Ki67免疫染色之间的定量关联。这些数据表明,TGF-α在雌激素受体阳性乳腺癌内分泌不敏感性的发生发展中起作用,其机制似乎独立于由Ki67免疫染色所确定的肿瘤生长分数。