Table 2.
Receptor | Strongest agonist | Signaling pathway | Effect | Reference |
---|---|---|---|---|
SSTR1 | All SSAs | Tyrosine phosphatase SHP-2 stimulation Induction of MAPK-ERK pathway and p21:Waf1:Cip1 Adenylyl cyclase modulation |
Cell cycle arrest Reduced metastatic potential |
[41, 52] |
SSTR2 | Vapreotide | Modulation of the ERK1/2 pathway and activation of SHP-1, SHP-2, and PTPη Modulation of the p21 and p27kip1 pathways Adenylyl cyclase modulation |
Apoptosis Cell cycle arrest; antineoplastic |
[82, 83, 87, 88] |
SSTR3 | Lanreotide | Adenylyl cyclase modulation | Apoptosis | [42, 94] |
SSTR4 | Octreotide | MAP kinase pathway, Ca2+-channels, K+-channels, and Na+-H+ antiporter Adenylyl cyclase modulation |
Cell cycle arrest | [41] |
SSTR5 | Octreotide | Guanylate cyclase inhibition and MAP kinase-ERK pathway Adenylyl cyclase modulation |
Cell cycle arrest Antineoplastic Apoptosis |
[41, 82, 84] |