Protein kinase C alpha expression in breast and ovarian cancer

被引:74
作者
Lahn, M [1 ]
Köhler, G
Sundell, K
Su, C
Li, SY
Paterson, BM
Bumol, TF
机构
[1] Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs, Div Oncol Prod Dev, Indianapolis, IN 46285 USA
[2] Eli Lilly & Co, Lilly Res Labs, Div Bioinformat, Indianapolis, IN 46285 USA
[3] Eli Lilly & Co, Lilly Res Labs, Div Biotechnol Discovery Res, Indianapolis, IN 46285 USA
[4] Univ Munster, Inst Pathol, D-4400 Munster, Germany
关键词
protein kinase C-alpha; breast cancer; ovarian cancer; estrogen receptor; gene array data; aprinocarsen; antisense oligonucleotide;
D O I
10.1159/000080279
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In recent years research has focused on the development of specific, targeted drugs to treat cancer. One approach has been to block intracellular signaling proteins, such as protein kinase C alpha (PKC-alpha). To help support the rationale for clinical studies of a PKC-alpha-targeted therapy in breast and ovarian cancers, we reviewed publications studying PKC-alpha expression in these tumors. Since these investigations were mostly performed in cell lines, we supplemented this review with some preliminary findings from studies examining PKC-alpha expression in tumor tissue biopsies obtained from patients with breast and ovarian cancer. Based on the reviewed publications using representative cell lines and our preliminary findings on tumor tissue of patients with breast cancer, we infer that PKC-alpha levels may especially be increased in breast cancer patients with low or negative estrogen receptor (ER) levels. Thus, clinical studies determining efficacy of selective or specific inhibitors of PKC-alpha should include determination of ER status in order to help answer whether blocking PKC-alpha in patients with low or absent ER can result in clinical benefit. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:1 / 10
页数:10
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