Activation of Signal Pathways and the Resistance to Anti-EGFR Treatment in Colorectal Cancer

被引:18
|
作者
Chen, Jiezhong [1 ,2 ]
Huang, Xu-Feng [1 ,2 ]
Katsifis, Andrew [3 ]
机构
[1] Univ Wollongong, Illawarra Hlth & Med Res Inst, Wollongong, NSW 2522, Australia
[2] Univ Wollongong, Sch Hlth Sci, Wollongong, NSW 2522, Australia
[3] ANSTO Life Sci, Lucas Heights, NSW, Australia
关键词
EGFR; KRAS; Src; PIK3CA; BRAF; GROWTH-FACTOR RECEPTOR; SRC FAMILY KINASES; ACQUIRED-RESISTANCE; 1ST-LINE TREATMENT; COLON-CANCER; WILD-TYPE; PTEN EXPRESSION; FACTOR AXIS; KRAS STATUS; CETUXIMAB;
D O I
10.1002/jcb.22905
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colorectal cancer is the third most common cancer with a 5-year survival rate of less than 10%. It is caused by alterations of multiple signal pathways which are affected by both genetic and environmental factors. In some cases, EGFR is important in the carcinogenesis of colorectal cancer suggesting anti-EGFR therapy may be a potential treatment option. However, in other cases it is not effective, which may be related to its down-stream targeted gene mutations. KRAS is highly emphasized in the literature but other mutations like Src, PIK3CA, and BRAF may also be important. Furthermore, obesity may decrease the effectiveness of anti-EGFR treatment as it increases the risk factors for colorectal cancer. Using next-generation sequencing technology, it may be possible to identify all gene mutations in an individual with colorectal cancer. Therefore, gene mutations affecting anti-EGFR therapy in colorectal cancer patients can be identified. J. Cell. Biochem. 111: 1082-1086, 2010. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:1082 / 1086
页数:5
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