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A novel approach to anticancer therapies: peroxisome proliferator activator-receptor-gamma as a new target therapy in the treatment of human urological cancer.

机译:一种新的抗癌治疗方法:过氧化物酶体增殖物激活剂-受体-γ作为治疗人类泌尿系统癌症的新靶标疗法。

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摘要

Peroxisome proliferator activator-receptor (PPAR)-gamma is a ligand-activated transcriptional factor belonging to a steroid receptor superfamily. PPAR-gamma plays a role in both adipocyte differentiation and carcinogenesis. Up-date, PPAR-gamma is expressed in various cancer tissues, and PPAR-gamma ligand induces growth arrest of these cancer cells. In this study, we examined the expression of PPAR-gamma in human urological cancer (including renal cell carcinoma, bladder tumor, prostate cancer and testicular cancer) by RT-PCR and immunohistochemistry, and we also examined the effect of PPAR-gamma ligand in these cells by MTT assay, flow cytometry and hoechest staining. PPAR-gamma expression was significantly more extensive and intense in malignant tissues than in normal tissues. PPAR-gamma ligand induced the reduction of malignant cell viability through early apoptosis. These results demonstrated that generated PPAR-gamma in urological cancer cells may play an important role in carcinogensis and become a new target therapy in the treatment of urological cancer.
机译:过氧化物酶体增殖物激活物受体(PPAR)-γ是一种类固醇激活的转录因子,属于类固醇受体超家族。 PPAR-γ在脂肪细胞分化和致癌作用中均起作用。最新,PPAR-γ在各种癌症组织中表达,并且PPAR-γ配体诱导这些癌细胞的生长停滞。在这项研究中,我们通过RT-PCR和免疫组织化学方法检查了PPAR-γ在人泌尿外科癌症(包括肾细胞癌,膀胱肿瘤,前列腺癌和睾丸癌)中的表达,并检查了PPAR-γ配体在人泌尿道恶性肿瘤中的作用。通过MTT测定,流式细胞术和最强染色对这些细胞进行染色。与正常组织相比,PPAR-γ在恶性组织中的表达更为广泛和强烈。 PPAR-γ配体通过早期凋亡诱导了恶性细胞活力的降低。这些结果表明,泌尿外科癌细胞中产生的PPAR-γ可能在致癌作用中起重要作用,成为泌尿外科癌症治疗的新靶标疗法。

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