Role of the tumor-associated trypsin inhibitor SPINK1 in cancer development.

I n most industrialized countries, prostate cancer is the most common non-skin cancer of men. When detected early, most cases are curable, but for tumors that have metastasized, there is no curative therapy. Pharmaceutical androgen ablation or castration induces remission in most patients with metastatic disease, but if the patient lives long enough, the tumor becomes androgenindependent. In some patients, chemotherapy induces remission, which mostly is of short duration. Therefore, new treatment modalities are needed for androgen-independent prostate cancer. Increasing knowledge of the biology of prostate cancer promises to facilitate development of therapies that target specific disease mechanisms. The recent finding of overexpression of serine protease inhibitor Kazal type 1 (SPINK1) in prostate cancer may represent a new mechanism amenable to targeted therapy in selected patients. SPINK1 was initially found in pancreatic tissue and pancreatic fluid and was therefore called pancreatic secretory trypsin inhibitor. When later identified in urine from patients with ovarian cancer, it was called tumor associated trypsin inhibitor. This name has been used in most studies on its role in cancer. SPINK1 occurs at high concentrations in the pancreas, where it functions as a first line of defense against premature activation of trypsinogen. This role of SPINK1 is demonstrated by the finding that a mutation in the SPINK1 gene is associated with increased risk of pancreatitis. High expression of SPINK1 in malignant diseases was first observed in ovarian cancer, but later this has been found in many other cancers. In most tumor types, this is associated with adverse prognosis. The Expression of SPINK1 is invariably associated with expression of tumor-associated trypsin, which activates several matrix metalloproteinases. Because these have been shown to mediate cancer invasion, the association between SPINK1 expression and adverse prognosis in cancer has been ascribed to the expression of trypsin by the tumors. This notion was supported by the finding of high tissue expression of trypsinogen-2 and adverse prognosis in ovarian cancer. In other tumors, low expression of SPINK1 is associated with adverse prognosis and aggressive disease, i.e., ventricular and bladder cancer. In these tumors, SPINK1 may inhibit tumor invasion by inhibiting protease cascades involving trypsin. Recent studies have revealed another function of SPINK1, i.e., it can promote development and growth of prostate cancer by stimulating the epidermal growth factor receptor (EGFR). The structure of SPINK1 resembles that of EGF; they have 50% sequence homology, a molecular size of approximately 6 kDa and three intrachain disulfide bridges. This prompted studies on the ability of SPINK1 to act as a growth factor. Early studies showed that SPINK1 binds to surface receptors and stimulates DNA synthesis of fibroblasts, but EGF and several other growth factors do not compete for binding of SPINK1. More recently, overexpression of SPINK1 in hepatocellular cancer has been shown to be strongly associated with high-stage, early tumor recurrence and short 5-year survival. SPINK1 has been identified in the medium of the colon cancer cell line HT29 5M21 by proteomic techniques and shown to be the major proinvasive factor produced by these cells. At physiological concentrations, recombinant SPINK1 increases invasion in collagen gel of several cell lines, but a SPINK1 mutant, SPINK1 K18Y, which does not inhibit trypsin, has no effect on invasion. Furthermore, an antibody to SPINK1 inhibits the invasiveness of HT29 5M21 cells. More recently, increased SPINK1 expression in tumor tissue and SPINK1 concentrations in serum have been shown to be independent prognostic factors for liver metastasis and adverse prognosis in colorectal cancer. SPINK1 is also expressed in the prostate and its expression increases with high tumor grade. Strongly increased SPINK1 expression is found in about 10% of all prostate cancers and this is associated with adverse prognosis. In surgically resected patients, increased SPINK1 expression is inversely related to gene fusions involving erythroblastosis virus E26 transformation–specific (ETS) family of transcriptions factors. However, in endocrine treated patients, this is not associated with adverse prognosis. New information on the mechanisms by which SPINK1 may be associated with adverse prognosis was provided by the recent study of Ateeq et al. Using several independent techniques, they showed that SPINK1 contributes to the aggressive phenotype of the prostate cancer cell line 22RV1. Forced expression of SPINK1 increases cell proliferation and invasiveness, while knockdown of the expression reduces these effects. Furthermore, the effect of SPINK1 on cell proliferation, invasion and growth of SPINK1-expressing tumor xenografts in mice was strongly reduced by a monoclonal antibody. Administration of antibodies to either SPINK1 or EGFR to mice bearing 22RV1 xenografts attenuated tumor growth by about 60% and 40%, respectively, while the effect of those combined was 75%. The neoplastic effects of SPINK1 were shown to be mediated by binding to EGFR, but other mechanisms Deparment of Clinical Chmistry, Helsinki University and Helsinki University Central Hospital, FIN-00014 Helsinki University, PB 63, Finland Correspondence: Dr U-H Stenman (ulf-hakan.stenman@ helsinki.fi) Asian Journal of Andrology (2011) 13, 628–629 2011 AJA, SIMM & SJTU. All rights reserved 1008-682X/11 $32.00