Overexpression of HMGA1 promotes anoikis resistance and constitutive Akt activation in pancreatic adenocarcinoma cells

被引:41
作者
S-S Liau [1 ]
A Jazag [1 ]
K Ito [1 ]
E E Whang [1 ]
机构
[1] Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115
基金
美国国家卫生研究院;
关键词
Akt; Anoikis; HMGA1; Pancreatic adenocarcinoma;
D O I
10.1038/sj.bjc.6603654
中图分类号
学科分类号
摘要
HMGA1 proteins are architectural transcription factors that are overexpressed by pancreatic adenocarcinomas. Roles of HMGA1 in mediating the malignant phenotype of this cancer are poorly understood. We tested the hypothesis that overexpression of HMGA1 promotes resistance to anoikis (apoptosis induced by anchorage deprivation) in pancreatic cancer cells. HMGA1 cDNA was stably transfected into MiaPaCa2 human pancreatic adenocarcinoma cells (which have low baseline expression levels of HMGA1). Cells were grown in suspension on PolyHEMA-coated plates and their susceptibility to anoikis was assayed using flow cytometry. Overexpression of HMGA1 was associated with marked reductions in susceptibility to anoikis in concert with increases in Akt phosphorylation (Ser473) and in Akt kinase activity and with reductions in caspase 3 activation. Inhibition of phosphoinositidyl-3 (PI3-K)/Akt pathway with either the small molecule inhibitor LY294002 or dominant-negative Akt resulted in reversal of anoikis resistance induced by HMGA1 overexpression. Further, RNA interference-mediated HMGA1 silencing in MiaPaCa2 and BxPC3 (a human pancreatic adenocarcinoma cell line with high baseline levels of HMGA1 expression) cells resulted in significant increases in susceptibility to anoikis. Our findings suggest HMGA1 promotes anoikis resistance through a PI3-K/Akt-dependent mechanism. Given the putative associations between anoikis resistance and metastatic potential, HMGA1 represents a potential therapeutic target in pancreatic adenocarcinoma. © 2007 Cancer Research.
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页码:993 / 1000
页数:7
相关论文
共 29 条
[1]  
Abe N., Watanabe T., Masaki T., Mori T., Sugiyama M., Uchimura H., Fujioka Y., Chiappetta G., Fusco A., Atomi Y., Pancreatic duct cell carcinomas express high levels of high mobility group I(Y) proteins, Cancer Res, 60, pp. 3117-3122, (2000)
[2]  
Balcerczak M., Pasz-Walczak G., Balcerczak E., Wojtylak M., Kordek R., Mirowski M., HMGI(Y) gene expression in colorectal cancer: Comparison with some histological typing, grading, and clinical staging, Pathol Res Pract, 199, pp. 641-646, (2003)
[3]  
Berezovskaya O., Schimmer A.D., Glinskii A.B., Pinilla C., Hoffman R.M., Reed J.C., Glinsky G.V., Increased expression of apoptosis inhibitor protein XIAP contributes to anoikis resistance of circulating human prostate cancer metastasis precursor cells, Cancer Res, 65, pp. 2378-2386, (2005)
[4]  
Chang Z.G., Yang L.Y., Wang W., Peng J.X., Huang G.W., Tao Y.M., Ding X., Determination of high mobility group A1 (HMGA1) expression in hepatocellular carcinoma: A potential prognostic marker, Dig Dis Sci, 50, pp. 1764-1770, (2005)
[5]  
Chiappetta G., Botti G., Monaco M., Pasquinelli R., Pentimalli F., Di Bonito M., D'Aiuto G., Fedele M., Iuliano R., Palmieri E.A., Pierantoni G.M., Giancotti V., Fusco A., HMGA1 protein overexpression in human breast carcinomas: Correlation with ErbB2 expression, Clin Cancer Res, 10, pp. 7637-7644, (2004)
[6]  
Chuma M., Saeki N., Yamamoto Y., Ohta T., Asaka M., Hirohashi S., Sakamoto M., Expression profiling in hepatocellular carcinoma with intrahepatic metastasis: Identification of high-mobility group I(Y) protein as a molecular marker of hepatocellular carcinoma metastasis, Keio J Med, 53, pp. 90-97, (2004)
[7]  
Czyz W., Balcerczak E., Jakubiak M., Pasieka Z., Kuzdak K., Mirowski M., HMGI(Y) gene expression as a potential marker of thyroid follicular carcinoma, Langenbecks Arch Surg, 389, pp. 193-197, (2004)
[8]  
Donato G., Martinez Hoyos J., Amorosi A., Maltese L., Lavano A., Volpentesta G., Signorelli F., Pentimalli F., Pallante P., Ferraro G., Tucci L., Signorelli C.D., Viglietto G., Fusco A., High mobility group A1 expression correlates with the histological grade of human glial tumors, Oncol Rep, 11, pp. 1209-1213, (2004)
[9]  
Douma S., Van Laar T., Zevenhoven J., Meuwissen R., Van Garderen E., Peeper D.S., Suppression of anoikis and induction of metastasis by the neurotrophic receptor TrkB, Nature, 430, pp. 1034-1039, (2004)
[10]  
Frasca F., Rustighi A., Malaguarnera R., Altamura S., Vigneri P., Del Sal G., Giancotti V., Pezzino V., Vigneri R., Manfioletti G., HMGA1 inhibits the function of p53 family members in thyroid cancer cells, Cancer Res, 66, pp. 2980-2989, (2006)