Therapeutic targeting of the phosphatidyl-inositol 3-kinase signaling pathway: novel targeted therapies and advances in the treatment of colorectal cancer

被引:27
作者
Yu, Ming [3 ]
Grady, William M. [1 ,2 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
[2] Univ Washington, Sch Med, Seattle, WA USA
[3] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
关键词
AKT; colorectal cancer; PI3; kinase; signaling; therapy; GROWTH-FACTOR RECEPTOR; TYROSINE KINASE INHIBITORS; PLECKSTRIN HOMOLOGY DOMAIN; PIK3CA GENE-MUTATIONS; NONSMALL CELL LUNG; ACQUIRED-RESISTANCE; TUMOR-SUPPRESSOR; PI3K PATHWAY; PHOSPHATIDYLINOSITOL-3-OH KINASE; MEK INHIBITORS;
D O I
10.1177/1756283X12448456
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Colorectal cancer (CRC) is one of the leading causes of cancer-related death in the USA, and more effective treatment of CRC is therefore needed. Advances in our understanding of the molecular pathogenesis of this malignancy have led to the development of novel molecule-targeted therapies. Among the most recent classes of targeted therapies being developed are inhibitors targeting the phosphatidylinositol 3-kinase (PI3K) signaling pathway. As one of the most frequently deregulated pathways in several human cancers, including CRC, aberrant PI3K signaling plays an important role in the growth, survival, motility and metabolism of cancer cells. Targeting this pathway therefore has considerable potential to lead to novel and more effective treatments for CRC. Preclinical and early clinical studies have revealed the potential efficacy of drugs that target PI3K signaling for the treatment of CRC. However, a major challenge that remains is to study these agents in phase III clinical trials to see whether these early successes translate into better patient outcomes. In this review we focus on providing an up-to-date assessment of our current understanding of PI3K signaling biology and its deregulation in the molecular pathogenesis of CRC. Advances in available agents and challenges in targeting the PI3K signaling pathway in CRC treatment will be discussed and placed in the context of the currently available therapies for CRC.
引用
收藏
页码:319 / 337
页数:19
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