Tazawa Hirofumi, Hato Shinji, Yoshino Shigefumi, Otsuka Shinya, Takeno Atsusi, Toyota Kazuhiro, Moriya Hiromitsu, Nozaki Isao, Tanakaya Koji, Uchiyama Hideaki, Saito Akihisa, Kuraoka Kazuya, Kato Takeshi, Suzuki Takahisa, Tashiro Hirotaka
Department of Surgery, NHO Kure Medical Center and Chugoku Cancer Center, 3-1, Aoyama, Kure, Hiroshima, 737-0023, Japan.
Department of Gastroenterological Surgery, NHO National Hospital Organization Shikoku Cancer Center, Matsuyama, Ehime, Japan.
Sci Rep. 2025 Mar 11;15(1):8385. doi: 10.1038/s41598-025-93422-6.
Transmembrane protease serine 4 (TMPRSS4) is a member of the type II transmembrane serine protease family known to be upregulated in many malignancies. We previously showed that TMPRSS4 may be a prognostic biomarker and therapeutic target for gastric cancer (GC), especially in stage III. In this retrospective study conducted at 10 institutions, all 325 patients underwent R0 resection involving D2 lymph node dissection. TMPRSS4 expression was examined using immunohistochemical analysis. TMPRSS4 expression was upregulated in 44.9% of participants. The 5-year overall survival (OS) of the TMPRSS4-positive group was significantly lower than that of the TMPRSS4-negative group (62.4% vs. 76.4%, respectively; p = 0.0149). Univariate analysis revealed that TMPRSS4 upregulation, tumor size, deeper tumor invasion, lymph node metastasis (N), lymphatic invasion, and tumor stage were significant prognostic factors for OS. Multivariate analysis revealed that N and TMPRSS4 upregulation were significant prognostic factors for OS. The 5-year OS rate was examined in two patient groups: the group with the receiver operating characteristic curve cut-off value ≥ 45% for TS-1 (cancer drug formulation) oral dosage and the group with TS-1 dosage cut-off value < 45%. For the patients in the TS-1 dosage ≥ 45% group, there were significant differences in OS between the TMPRSS4-positive and -negative groups (p = 0.0284): the 5-year OS rates of TMPRSS4-positive and -negative groups were 65.2% and 79.2%, respectively. Our findings suggest that TMPRSS4 overexpression is a useful biomarker for GC, and that an anti-TMPRSS4 antibody may have potential as a novel therapeutic agent.
跨膜蛋白酶丝氨酸4(TMPRSS4)是II型跨膜丝氨酸蛋白酶家族的成员,已知在许多恶性肿瘤中上调。我们之前表明,TMPRSS4可能是胃癌(GC)的预后生物标志物和治疗靶点,尤其是在III期。在这项在10家机构进行的回顾性研究中,所有325例患者均接受了包括D2淋巴结清扫的R0切除。使用免疫组织化学分析检测TMPRSS4表达。44.9%的参与者中TMPRSS4表达上调。TMPRSS4阳性组的5年总生存率(OS)显著低于TMPRSS4阴性组(分别为62.4%和76.4%;p = 0.0149)。单因素分析显示,TMPRSS4上调、肿瘤大小、肿瘤浸润深度、淋巴结转移(N)、淋巴管浸润和肿瘤分期是OS的显著预后因素。多因素分析显示,N和TMPRSS4上调是OS的显著预后因素。在两个患者组中检查了5年OS率:TS-1(抗癌药物制剂)口服剂量的受试者工作特征曲线截止值≥45%的组和TS-1剂量截止值<45%的组。对于TS-1剂量≥45%组的患者,TMPRSS4阳性和阴性组之间的OS存在显著差异(p = 0.0284):TMPRSS4阳性和阴性组的5年OS率分别为65.2%和79.2%。我们的研究结果表明,TMPRSS4过表达是GC的一种有用生物标志物,抗TMPRSS4抗体可能具有作为新型治疗药物的潜力。