mTOR, translational control and human disease

AR Tee, J Blenis - Seminars in cell & developmental biology, 2005 - Elsevier
Seminars in cell & developmental biology, 2005Elsevier
Many human diseases occur when the precise regulation of cell growth (cell mass/size) and
proliferation (rates of cell division) is compromised. This review highlights those human
disorders that occur as a result of inappropriate cellular signal transduction through the
mammalian target of rapamycin (mTOR), a major pathway that coordinates proper cell
growth and proliferation by regulating ribosomal biogenesis and protein translation. Recent
studies reveal that the tuberous sclerosis complex (TSC)-1/2, PTEN, and LKB1 tumor …
Many human diseases occur when the precise regulation of cell growth (cell mass/size) and proliferation (rates of cell division) is compromised. This review highlights those human disorders that occur as a result of inappropriate cellular signal transduction through the mammalian target of rapamycin (mTOR), a major pathway that coordinates proper cell growth and proliferation by regulating ribosomal biogenesis and protein translation. Recent studies reveal that the tuberous sclerosis complex (TSC)-1/2, PTEN, and LKB1 tumor suppressor proteins tightly control mTOR. Loss of these tumor suppressors leads to an array of hamartoma syndromes as a result of heightened mTOR signaling. Since mTOR plays a pivotal role in maintaining proper cell size and growth, dysregulation of mTOR signaling results in these benign tumor syndromes and an array of other human disorders.
Elsevier