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those success rates. Both drugs, evolocumab (Repatha) and alirocumab (Praluent), are used to
treat some people with high cholesterol. The drugs are also less expensive than most cancer
treatments and patients can take the medicines at home. In lab experiments, cancer cells
engineered to lack PCSK9 (by deleting the gene for the enzyme) grew at the same rate as cancer
cells with PCSK9. PCSK9 affects blood cholesterol levels by controlling how much cholesterol
receptor, a claw-like protein that grabs onto cholesterol and brings it inside, sits on the surface of
liver cells. Blocking PCSK9 leads to more cholesterol receptors on cell surfaces and, in turn, less
cholesterol in the blood. Although PCSK9 is best known for its influence on the cholesterol
receptor, it also controls the levels of other receptors on cells, including some that are involved in
immune responses. The researchers found that PCSK9 affects how much MHC I sits on the
surface of cancer cells. Deleting PCSK9 or blocking its activity with evolocumab substantially
raised the amount of MHC I on the surfaces of skin and breast cancer cells. In addition,
PCSK9-deleted tumors contained more cancer-killing immune cells, including T cells, than
Huang, B., Zhang, H., Gu, L., Ye, B., Jian, Z., Stary, C., & Xiong, X. (2017). Advances in
doi:10.1155/2017/3597613