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Purification and Aggregation of the Amyloid Precursor Protein Intracellular Domain
Published on: August 28, 2012
Apolipoprotein A-I and Cancer
Maryam Zamanian-Daryoush1, Joseph A DiDonato1
1Department of Cellular and Molecular Medicine, and Center for Cardiovascular Diagnostics and Prevention, Cleveland Clinic, Cleveland OH, USA.
Insights
Apolipoprotein A-I (apoA-I) and high-density lipoprotein (HDL) show protective effects against cancer development. Increasing apoA-I/HDL levels may prevent tumors, and apoA-I shows therapeutic potential in established cancers.
Area of Science:
- Cardiovascular Science
- Oncology
- Biochemistry
Background:
- High-density lipoprotein (HDL) and apolipoprotein A-I (apoA-I) are crucial in reverse cholesterol transport and cardiovascular disease.
- Recent clinical studies suggest an inverse relationship between HDL-cholesterol (HDL-C) levels and cancer risk.
Purpose of the Study:
- To review the emerging role of apoA-I in tumor biology.
- To discuss the potential of apoA-I as a cancer therapeutic.
Main Methods:
- Review of clinical studies noting HDL-C and cancer risk.
- Analysis of mouse tumor studies investigating apoA-I/HDL effects.
Main Results:
- Mouse studies confirm a protective role for increased apoA-I/HDL against tumor development.
- Administration of human apoA-I demonstrated therapeutic efficacy against established tumors.
Conclusions:
- ApoA-I/HDL exhibits significant anti-tumor properties.
- ApoA-I represents a promising therapeutic target for cancer treatment.
Abstract:
High-density lipoprotein (HDL) and apolipoprotein A-I (apoA-I), the predominant protein in plasma HDL, have long been the focus of intense studies in the field of atherosclerosis and cardiovascular disease. ApoA-I, in large part, is responsible for HDL assembly and its main atheroprotective function, that of shuttling excess cholesterol from peripheral tissues to the liver for excretion (reverse cholesterol transport). Recently, a protective role for HDL in cancer was suggested from several large clinical studies where an inverse relationship between plasma HDL-cholesterol (HDL-C) levels and risk of developing cancer was noted. This notion has now been tested and found to be supported in mouse tumor studies, where increasing levels of apoA-I/HDL were discovered to protect against tumor development and provision of human apoA-I was therapeutic against established tumors. This mini-review discusses the emerging role of apoA-I in tumor biology and its potential as cancer therapeutic.
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