The Gene Expression Status of the PI3K/AKT/mTOR Pathway in Gastric Cancer Tissues and Cell Lines

被引:112
作者
Riquelme, Ismael [1 ,2 ]
Tapia, Oscar [1 ]
Espinoza, Jaime A. [3 ,4 ,5 ]
Leal, Pamela [6 ]
Buchegger, Kurt [1 ,2 ]
Sandoval, Alejandra [4 ,5 ]
Bizama, Carolina [3 ,4 ,5 ]
Carlos Araya, Juan [7 ]
Peek, Richard M. [8 ]
Carlos Roa, Juan [3 ,4 ,5 ]
机构
[1] Univ La Frontera, Sch Med, Dept Pathol Anat, Lab Mol Pathol, Ave Alemania 0458, Temuco 4810296, Chile
[2] Univ La Frontera, Sci & Technol Bioresource Nucleus BIOREN, Ave Francisco Salazar 01145,Casilla 54-D, Temuco, Chile
[3] Pontificia Univ Catolica Chile, Dept Pathol, Marcoleta 377,7th Floor, Santiago 8330024, Chile
[4] Pontificia Univ Catolica Chile, Sch Med, UC Ctr Invest Oncol CITO, Portugal 61, Santiago 8330034, Chile
[5] Pontificia Univ Catolica Chile, Adv Ctr Chron Dis ACCDiS, Marcoleta 377,7th Floor, Santiago 8330024, Chile
[6] Univ La Frontera, Mol Biol & Biomed Lab, CEGIN BIOREN, Ave Alemania 0458, Temuco 4810296, Chile
[7] Univ La Frontera, Sch Med, Dept Pathol Anat, Ave Alemania 0458, Temuco 4810296, Chile
[8] Vanderbilt Univ, Sch Med, Div Gastroenterol, Dept Med & Canc Biol, 2215 Garland Ave Nashville, Nashville, TN 37232 USA
关键词
PI3K/AKT/mTOR pathway; Gastric cancer; AGS; MKN28 and MKN45 cell lines; SIGNALING PATHWAY; UP-REGULATION; MTOR; THERAPY; PROGRESSION; TARGET; CARCINOGENESIS; ADENOCARCINOMA; CARCINOMAS; PTEN;
D O I
10.1007/s12253-016-0066-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The PI3K/AKT/mTOR pathway plays a crucial role in the regulation of multiple cellular functions including cell growth, proliferation, metabolism and angiogenesis. Emerging evidence has shown that deregulation of this pathway has a role promoting gastric cancer (GC). The aim was to assess the expression of genes involved in this pathway by qPCR in 23 tumor and 23 non-tumor gastric mucosa samples from advanced GC patients, and in AGS, MKN28 and MKN45 gastric cancer cell lines. Results showed a slight overexpression of PIK3CA, PIK3CB, AKT1, MTOR, RPS6KB1, EIF4EBP1 and EIF4E genes, and a slightly decreased PTEN and TSC1 expression. In AGS, MKN28 and MKN45 cells a significant gene overexpression of PIK3CA, PIK3CB, AKT1, MTOR, RPS6KB1 and EIF4E, and a significant repression of PTEN gene expression were observed. Immunoblotting showed that PI3K-beta, AKT, p-AKT, PTEN, mTOR, p-mTOR, P70S6K1, p-P70S6K1, 4E-BP1, p-4E-BP1, eIF4E and p-eIF4E proteins were present in cell lines at different levels, confirming activation of this pathway in vitro. This is the first time this extensive panel of 9 genes within PI3K/AKT/mTOR pathway has been studied in GC to clarify the biological role of this pathway in GC and develop new strategies for this malignancy.
引用
收藏
页码:797 / 805
页数:9
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