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组织蛋白酶B和胱抑素C在卵巢癌侵袭机制中的作用。

The role of cathepsin B and cystatin C in the mechanisms of invasion by ovarian cancer.

作者信息

Nishikawa Hiroshi, Ozaki Yasuhiko, Nakanishi Tamao, Blomgren Klas, Tada Toyohiro, Arakawa Atsushi, Suzumori Kaoru

机构信息

Department of Obstetrics and Gynecology, Nagoya City University Medical School, Mizuho-cho, Mizuho, Nagoya 467-8601, Japan.

出版信息

Gynecol Oncol. 2004 Mar;92(3):881-6. doi: 10.1016/j.ygyno.2003.11.017.

Abstract

OBJECTIVE

The aim of this study was to investigate the contribution of cathepsin B and cystatin C to the mechanisms of invasion by ovarian cancer.

MATERIALS AND METHODS

Using surgical materials from patients with ovarian cancer, immunohistochemistry, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting analysis were performed using antibodies against cathepsin B or cystatin C. Serum levels of cathepsin B and cystatin C in patients with benign and malignant ovarian lesions were determined by enzyme-linked immunosorbent assay (ELISA). An invasion assay using an ovarian cancer cell line was performed by addition of cystatin C or specific inhibitors of cathepsin B.

RESULTS

While immunohistochemical staining of cathepsin B and cystatin C was evident in cancer cells and associated stromal tissue, this was not the case in benign tumors. The malignancies were also found to be positive for cathepsin B and cystatin C by SDS-PAGE and Western blotting analysis. No significant difference in serum cathepsin B levels was observed between patients with benign and malignant disease. However, the concentration of cystatin C in cases with ovarian cancer was significantly higher in benign cases (P<0.0001) and in healthy controls (P<0.0001). Invasion by cancer cells was dose-dependently suppressed by cystatin C and cathepsin B inhibitors.

CONCLUSION

The results provided convincing evidence that cathepsin B and cystatin C may contribute to the mechanisms of invasion of ovarian cancer.

摘要

目的

本研究旨在探讨组织蛋白酶B和胱抑素C在卵巢癌侵袭机制中的作用。

材料与方法

利用卵巢癌患者的手术材料,采用抗组织蛋白酶B或胱抑素C的抗体进行免疫组织化学、十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质印迹分析。通过酶联免疫吸附测定(ELISA)测定良性和恶性卵巢病变患者血清中组织蛋白酶B和胱抑素C的水平。通过添加胱抑素C或组织蛋白酶B的特异性抑制剂,使用卵巢癌细胞系进行侵袭试验。

结果

组织蛋白酶B和胱抑素C在癌细胞及相关基质组织中的免疫组织化学染色明显,但在良性肿瘤中并非如此。通过SDS-PAGE和蛋白质印迹分析还发现恶性肿瘤组织蛋白酶B和胱抑素C呈阳性。良性和恶性疾病患者血清组织蛋白酶B水平未观察到显著差异。然而,卵巢癌患者中胱抑素C的浓度在良性病例(P<0.0001)和健康对照(P<0.0001)中显著更高。胱抑素C和组织蛋白酶B抑制剂可剂量依赖性地抑制癌细胞的侵袭。

结论

结果提供了令人信服的证据,表明组织蛋白酶B和胱抑素C可能参与卵巢癌的侵袭机制。

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