Edwards Joanne, Traynor Pamela, Munro Alison F, Pirret Catherine F, Dunne Barbara, Bartlett John M S
Endocrine Cancer Group, Division of Cancer Sciences and Molecular Pathology, Glasgow Royal Infirmary, Glasgow, United Kingdom.
Clin Cancer Res. 2006 Jan 1;12(1):123-30. doi: 10.1158/1078-0432.CCR-05-1445.
The role of the type I receptor tyrosine kinase (HER) family in progression of prostate cancer is controversial. Breast cancer studies show that these receptors should be investigated as a family. The current study investigates expression of HER1-HER4 and EGFRvIII in matched hormone-sensitive and hormone-refractory prostate tumors.
Immunohistochemical analysis was used to investigate protein expression of HER1-HER4, EGFRvIII, and phosphorylated Akt (pAkt) in matched hormone-sensitive and hormone-refractory prostate tumors.
Surprisingly, high HER2 membrane expression in hormone-sensitive tumors was associated with an increased time to biochemical relapse (P = 0.0003), and this translated into longer overall survival (P = 0.0021). Consistent with other studies, HER4 membrane expression in hormone-sensitive tumors was associated with longer time to biochemical relapse (P = 0.042), and EGFRvIII membrane expression was associated with shorter time to biochemical relapse (P = 0.015). An increase in pAkt expression was associated with reduced survival (P = 0.0098). Multivariate analysis showed that HER2 was an independent positive predictive marker of time to relapse in hormone-sensitive prostate tumors (P = 0.014). In contrast, high HER2 expression in hormone-refractory tumors was associated with decreased time to death from biochemical relapse (P = 0.039), and EGFRvIII nuclear expression was associated with decreased time to death from biochemical relapse and decreased overall survival (P = 0.02 and P = 0.005).
These results suggest that the HER family may have multiple roles in prostate cancer, and that expression of the proteins alone is insufficient to predict the biological response that they may elicit.
I型受体酪氨酸激酶(HER)家族在前列腺癌进展中的作用存在争议。乳腺癌研究表明,这些受体应作为一个家族进行研究。本研究调查了HER1-HER4和EGFRvIII在配对的激素敏感性和激素难治性前列腺肿瘤中的表达。
采用免疫组织化学分析方法,研究HER1-HER4、EGFRvIII和磷酸化Akt(pAkt)在配对的激素敏感性和激素难治性前列腺肿瘤中的蛋白表达。
令人惊讶的是,激素敏感性肿瘤中HER2高膜表达与生化复发时间延长相关(P = 0.0003),这转化为更长的总生存期(P = 0.0021)。与其他研究一致,激素敏感性肿瘤中HER4膜表达与生化复发时间延长相关(P = 0.042),而EGFRvIII膜表达与生化复发时间缩短相关(P = 0.015)。pAkt表达增加与生存期缩短相关(P = 0.0098)。多变量分析显示,HER2是激素敏感性前列腺肿瘤复发时间的独立阳性预测标志物(P = 0.014)。相比之下,激素难治性肿瘤中HER2高表达与生化复发导致的死亡时间缩短相关(P = 0.039),而EGFRvIII核表达与生化复发导致的死亡时间缩短和总生存期缩短相关(P = 0.02和P = 0.005)。
这些结果表明,HER家族在前列腺癌中可能具有多种作用,仅蛋白表达不足以预测它们可能引发的生物学反应。