2014
DOI: 10.1016/j.tem.2013.11.003
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Somatostatin analogs: does pharmacology impact antitumor efficacy?

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Cited by 58 publications
(62 citation statements)
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“…SST receptor 1-5 are responsible for activation of protein tyrosine phosphatases (PTP) which via various downstream pathways as described by Chalabi et al [17] ''ERK1/2, phosphoinositide 3-kinase (PI3 K), AKT, nitric oxide synthase (NOS), and cGMP-dependent protein kinase'' results in induction of a cyclin-dependent kinase inhibitor [18]. End result of this cascade results in pro-apoptosis, inhibition of cell migration, and arrest of cell cycle.…”
Section: Discussionmentioning
confidence: 99%
“…SST receptor 1-5 are responsible for activation of protein tyrosine phosphatases (PTP) which via various downstream pathways as described by Chalabi et al [17] ''ERK1/2, phosphoinositide 3-kinase (PI3 K), AKT, nitric oxide synthase (NOS), and cGMP-dependent protein kinase'' results in induction of a cyclin-dependent kinase inhibitor [18]. End result of this cascade results in pro-apoptosis, inhibition of cell migration, and arrest of cell cycle.…”
Section: Discussionmentioning
confidence: 99%
“…Also as a secondary effect, somatostatin analogues, like VEGF inhibitors, also affect tumor vascularization; this may be of special importance due to the highly vascular nature of the pituicytoma itself . As pituicytoma samples in our study stained mainly for SSTR 3 and 5, the use of, for example, pasireotide with a high affinity to those receptors may be a potential option . This agent has so far been approved for the use as a second line treatment in Cushing's disease and acromegaly and shown good clinical results including tumor mass reduction,…”
Section: Discussionmentioning
confidence: 74%
“…Two methodologically different treatment alternatives exist in this sector. Somatostatin receptor analogues are ligands to the receptor inducing cell cycle arrest and a downregulation of protein biosynthesis therefore creating an imbalance toward increased apoptosis within the affected stroma . Also as a secondary effect, somatostatin analogues, like VEGF inhibitors, also affect tumor vascularization; this may be of special importance due to the highly vascular nature of the pituicytoma itself .…”
Section: Discussionmentioning
confidence: 99%
“…The signaling pathways used by these receptors are tightly controlled, highly specific, and are complicated by networking with many other molecules. Because somatostatin analogs have recently been shown to improve progression-free survival and control symptoms related to hypersecretion, they became a first-line therapy [5] .…”
Section: Net Therapeutic Targetsmentioning
confidence: 99%