Comprehensive analysis of oncogenic effects of PIK3CA mutations in human mammary epithelial cells

被引:0
作者
Haijun Zhang
Gang Liu
Michele Dziubinski
Zengquan Yang
Stephen P. Ethier
Guojun Wu
机构
[1] Karmanos Cancer Institute,Breast Cancer Program
[2] Southeast University School of Medicine,Genetics Research Center
[3] Wayne State University,Karmanos Cancer Institute, Department of Pathology
来源
Breast Cancer Research and Treatment | 2008年 / 112卷
关键词
PIK3CA; Breast cancer; Somatic mutation;
D O I
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中图分类号
学科分类号
摘要
More than 20 different PIK3CA gene mutations were identified in breast cancer with different frequencies. Whether these breast cancer associated mutations have similar biological effects is largely unknown. In this study, we established a novel cell model using the lentivirus system to express 10 different PIK3CA genes (wild type and mutant) based on the human mammary epithelial cell MCF10A. We found that nine different PIK3CA mutants harbor different abilities to promote cell proliferation and EGF independent growth. In addition, most PIK3CA mutants (except for the wild type PIK3CA, the Q60K and the K111N mutants) had the ability to change the morphogenesis of the MCF10A cell in 3D Matrigel assay. Moreover, different PIK3CA mutants have different abilities to promote colony formation and cell invasion. We further observed that most of the PIK3CA mutants could activate p-AKT and p-p70-S6K in the absence of EGF stimulation. Finally, LY294002, a PI3K inhibitor, can effectively inhibit cell growth in cell lines with different PIK3CAs. Taken together, our results support the notion that different PIK3CA mutations differentially contribute to breast cancer transformation, and exploration of the therapeutic application of these mutations will benefit breast cancer patients with the PIK3CA mutations.
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页码:217 / 227
页数:10
相关论文
共 243 条
[1]  
Leevers SJ(1999)Signalling through phosphoinositide 3-kinases: the lipids take centre stage Curr Opin Cell Biol 11 219-225
[2]  
Vanhaesebroeck B(2002)The phosphatidylinositol 3-Kinase AKT pathway in human cancer Nat Rev Cancer 2 489-501
[3]  
Waterfield MD(2005)Oncogenic PI3K deregulates transcription and translation Nat Rev Cancer 5 921-929
[4]  
Vivanco I(2002)The phosphoinositide 3-kinase pathway Science 296 1655-1657
[5]  
Sawyers CL(2006)Signalling through Class I PI3Ks in mammalian cells Biochem Soc Trans 34 647-662
[6]  
Bader AG(1998)DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies Am J Pathol 152 1107-1123
[7]  
Kang S(2000)Comparative genomic hybridization reveals complex genetic changes in primary breast cancer tumors and their cell lines Cancer Genet Cytogenet 119 132-138
[8]  
Zhao L(1999)Comparative genomic hybridization and chromosomal instability in solid tumours Br J Cancer 80 862-873
[9]  
Vogt PK(2000)PIK3CA as an oncogene in cervical cancer Oncogene 19 2739-2744
[10]  
Cantley LC(1999)Expression analysis of genes at 3q26-q27 involved in frequent amplification in squamous cell lung carcinoma Eur J Cancer 35 641-646