Analysis of whole genomic expression profiles and screening of the key signaling pathways associated with pancreatic cancer

被引：0

作者：

He, Chengzhi ^{[1
,2
]}

Jiang, Hua ^{[1
]}

Geng, Shasha ^{[1
]}

Sheng, Haihui ^{[3
]}

Shen, Xiaoying ^{[3
]}

Zhang, Xiaoyan ^{[3
]}

Zhu, Shizhang ^{[3
]}

Chen, Ximei ^{[2
]}

Yang, Changqing ^{[2
]}

Gao, HengJun ^{[2
,3
]}

机构：

[1] Tongji Univ, Shanghai E Hosp, Dept Gastroenterol, Sch Med, Shanghai 200120, Peoples R China

[2] Tongji Univ, Sch Med, Tongji Hosp, Dept Gastroenterol,Inst Digest Dis, Shanghai 200065, Peoples R China

[3] Natl Engn Ctr Biochip, Shanghai 201203, Peoples R China

来源：

INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2012年 / 5卷 / 06期

关键词：

Pancreatic cancer; microarray; gene expression profile; signaling pathway; ACUTE LYMPHOBLASTIC-LEUKEMIA; MARKERS; ADENOCARCINOMA; IDENTIFICATION; PROTEIN-1; INDUCTION; RECEPTOR; HEDGEHOG; TARGET; DOMAIN;

D O I：

暂无

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

The tumorigenesis of pancreatic cancer is thought to be a complex process. Investigation of the molecular mechanism of pancreatic cancer and exploring the specific markers for early diagnosis and specific targets of therapy is a key point to prevent and treat pancreatic cancer effectively and to improve their prognosis. In this study, expression profiles experiment was performed using Agilent human whole genomic oligonucleotide microarrays with 41,000 genes. Differentially expressed genes related with pancreatic cancer were screened, and analyzed further by GO term analysis and KEGG Pathway analysis. Our results showed that there were 1276 differentially expressed genes associated with pancreatic cancer. 691 genes were up regulated and 585 were down regulated in pancreatic cancer group. The present study confirmed that the occurrence of pancreatic cancer was involved in multiple-gene interaction. In addition, our study found that pancreatic cancer was related to an activation of the mTOR signaling pathway and renal cell carcinoma pathway.

引用

页码：537 / 546

页数：10

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