Anti-invasive, antitumorigenic, and antimetastatic activities of the PHSCN sequence in prostate carcinoma

Using naturally serum-free SU-ECM basement membranes as invasion substrates showed that plasma fibronectin was necessary to stimulate invasion by DU 145 human and metastatic MATLyLu (MLL) rat prostate carcinoma cells. This activity mapped to the PHSRN sequence, which induced invasion through α5β1 integrin. PHSCN, a competitive inhibitor, blocked both PHSRN- and serum-induced invasion. Acetylated, amidated PHSCN (Ac-PHSCN-NH₂) was 30- fold more potent; however, AcHSPNC-NH₂ was inactive. Rats receiving injections s.c. with 100,000 MLL cells were treated systemically by i.v. injection three times weekly with 1 mg of either Ac-PHSCN-NH₂ or Ac-HSPNC- NH₂ beginning 24 h later, three times weekly with 1 mg of Ac-PHSCN-NH₂ beginning only after surgery to remove large (2 cm) MLL tumors, or were left untreated. MLL tumors grew rapidly in Ac-HSPNC-NH₂-treated and in untreated rats. MLL tumor growth in rats treated with Ac-PHSCN-NH₂ beginning 1 day after MLL cell injection was reduced by 99.9% during the first 16 days of treatment, although subsequent tumor growth occurred. MLL tumor cryosections immunostained with anti-PECAM-1 showed that AcPHSCN-NH₂ inhibited neovascularization by 12-fold during this time. Whether initiated after MLL cell injection or only after MLL tumor removal, Ac-PHSCN-NH₂ treatment reduced the numbers of MLL lung colonies and micrometastases by 40- to >100- fold, whereas Ac-HSPNC-NH₂ was inactive. Thus, Ac-PHSCN-NH₂ may be a potent antitumorigenic and antimetastatic agent for postsurgical use prior to extensive metastasis.