The PI3K/AKT pathway as a target for cancer treatment

Ingrid A. Mayer; Carlos L. Arteaga

doi:10.1146/annurev-med-062913-051343

The PI3K/AKT pathway as a target for cancer treatment

Ingrid A. Mayer, Carlos L. Arteaga

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617 Scopus citations

Abstract

Anticancer targeted therapies are designed to exploit a particular vulnerability in the tumor, which in most cases results from its dependence on an oncogene and/or loss of a tumor suppressor. Genes in the phosphoinositide 3-kinase (PI3K)/AKT pathway are the most frequently altered in human cancers. Aberrant activation of this pathway, as a result of these somatic alterations, is associated with cellular transformation, tumorigenesis, cancer progression, and drug resistance. Several drugs targeting PI3K/ATK are currently in clinical trials, alone or in combination, in both solid tumors and hematologic malignancies. These drugs are the focus of this review.

Original language	English (US)
Pages (from-to)	11-28
Number of pages	18
Journal	Annual review of medicine
Volume	67
DOIs	https://doi.org/10.1146/annurev-med-062913-051343
State	Published - Jan 14 2016

Keywords

Breast cancer
Lymphoproliferative disorders
Mammalian target of rapamycin (mTOR)
Mutation
Pathway inhibitors
Phosphoinositide 3-kinase (PI3K)/AKT

ASJC Scopus subject areas

General Biochemistry, Genetics and Molecular Biology

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10.1146/annurev-med-062913-051343

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abstract = "Anticancer targeted therapies are designed to exploit a particular vulnerability in the tumor, which in most cases results from its dependence on an oncogene and/or loss of a tumor suppressor. Genes in the phosphoinositide 3-kinase (PI3K)/AKT pathway are the most frequently altered in human cancers. Aberrant activation of this pathway, as a result of these somatic alterations, is associated with cellular transformation, tumorigenesis, cancer progression, and drug resistance. Several drugs targeting PI3K/ATK are currently in clinical trials, alone or in combination, in both solid tumors and hematologic malignancies. These drugs are the focus of this review.",

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AB - Anticancer targeted therapies are designed to exploit a particular vulnerability in the tumor, which in most cases results from its dependence on an oncogene and/or loss of a tumor suppressor. Genes in the phosphoinositide 3-kinase (PI3K)/AKT pathway are the most frequently altered in human cancers. Aberrant activation of this pathway, as a result of these somatic alterations, is associated with cellular transformation, tumorigenesis, cancer progression, and drug resistance. Several drugs targeting PI3K/ATK are currently in clinical trials, alone or in combination, in both solid tumors and hematologic malignancies. These drugs are the focus of this review.

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The PI3K/AKT pathway as a target for cancer treatment

Abstract

Keywords

ASJC Scopus subject areas

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