Abstract

BackgroundTransmembrane serine protease 4 (TMPRSS4) belongs to the family of type II transmembrane serine proteases that are known to be upregulated in many malignant tumors. However, there is a paucity of studies documenting the clinical impact and biological effects of TMPRSS4 on gastric cancer (GC) patients who underwent surgery. MethodsTissues samples were obtained from 105 patients with GC who underwent gastrectomy followed by adjuvant chemotherapy, excluding those at stage I. The expression of TMPRSS4 was examined through immunohistochemical analysis. The association between TMPRSS4 expression and clinico-pathological features as well as prognosis was assessed. Moreover, the effects of TMPRSS4 expression on cell migration and sensitivity to 5-FU were investigated. ResultsThe expression rate of TMPRSS4 was 56.3% (59/105) in GC cases. The expression of TMPRSS4 was positively correlated with the depth of tumor (T) and venous (V) invasion. The 5-year overall survival (OS) and recurrence-free survival (RFS) rates of the TMPRSS4-positive group was significantly lower than that of the TMPRSS4-negative group (p=0.0001 and p=0.005, respectively). Especially, there was significant differences in OS and RFS of patients with stage III cancer between the two groups (p=0.0064 and 0.012, respectively). Multivariate analysis demonstrated that TMPRSS4 expression and the stage of cancer were crucial prognostic factors for RFS. TMPRSS4-silenced GC cells exhibited increased sensitivity to 5-FU when compared with the non-specific control siRNA-transfected cells. ConclusionTMPRSS4 can be considered as a potential prognostic biomarker, especially for stage III, and a promising therapeutic target for GC.

Highlights

  • Surgery is considered as the main treatment method for operable gastric cancer (GC)

  • We evaluated whether the expression of TMPRSS4 is associated with the clinico-pathological factors and the outcomes after gastrectomy for the patients with GC

  • We examined the effect of TMPRSS4 expression in vitro on the proliferation, migration, and the sensitivity to chemotherapy of GC cells

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Summary

Introduction

Surgery is considered as the main treatment method for operable gastric cancer (GC). Appreciable patients at stages II and III undergo recurrence. Various adjuvant chemotherapy methods have been developed and tested to prevent postoperative recurrence. In 2007, the Adjuvant Chemotherapy Trial of S-1 for GC (ACTS-GC) demonstrated that surgery in addition to a 12 months of postoperative adjuvant chemotherapy with S-1 improved the overall survival (OS) and recurrence-free survival (RFS) rates compared to surgery alone for patients at stages II and III of GC. . The 5-year OS rate in patients at stages IIIA and IIIB were 67.1 and 50.2% in the S-1 group, respectively, indicating the need for further improvement. There is a paucity of studies documenting the clinical impact and biological effects of TMPRSS4 on gastric cancer (GC) patients who underwent surgery

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