INSERM U 895, C3M, University of Nice Sophia Antipolis, 151 route Saint-Antoine de Ginestière, BP 2 3194, 06204 Nice, France.
Hum Pathol. 2011 Dec;42(12):1841-8. doi: 10.1016/j.humpath.2010.05.033. Epub 2011 Jun 17.
Infertility has been stated as a risk factor for testicular cancer; but currently, there is no prognostic indicator of tumor development from the pathologic testis with impaired spermatogenesis. Regenerating proteins are expressed in many human tissues including the testis, and their role in carcinogenesis has been well documented. In the present work, regenerating I messenger RNA and protein expression and cellular protein localization were studied in testicular biopsies of patients with normal (obstructive azoospermia) or impaired spermatogenesis (nonobstructive azoospermia) and in seminoma testis by quantitative reverse transcriptase-polymerase chain reaction, Western blot, and immunofluorescence analyses. No significant differences in regenerating I transcripts were reported between the 3 groups studied. However, regenerating I protein was highly expressed in pure seminoma and in placental-like alkaline phosphatase-positive seminiferous tubules with in situ carcinoma. Regenerating I protein levels measured by Western blotting increased from the placental-like alkaline phosphatase-negative distal region of the seminoma to the pure placental-like alkaline phosphatase-positive tumoral region. Importantly, although cells localized in seminiferous tubules of obstructive azoospermic patients with normal spermatogenesis were very slightly labeled, persisting germ, Sertoli, and myoid cells and fibrous tissues were strongly regenerating I positive in seminiferous tubules of nonobstructive azoospermia. These results suggest the possibility to use regenerating I as a prognostic marker of tumoral development in the infertile testis.
不育症已被认为是睾丸癌的一个危险因素;但目前,对于生精功能受损的病理性睾丸,尚无肿瘤发展的预后指标。再生蛋白在许多人体组织中表达,包括睾丸,其在致癌作用中的作用已有充分的文献记载。在本研究中,通过定量逆转录聚合酶链反应、Western blot 和免疫荧光分析,研究了正常(梗阻性无精子症)或生精功能受损(非梗阻性无精子症)患者睾丸活检以及精原细胞瘤睾丸中再生 I 信使 RNA 和蛋白表达及细胞蛋白定位。研究报告称,3 组研究对象的再生 I 转录本无显著差异。然而,在纯精原细胞瘤和胎盘样碱性磷酸酶阳性、原位癌的精曲小管中,再生 I 蛋白高度表达。通过 Western blot 测量的再生 I 蛋白水平从胎盘样碱性磷酸酶阴性的精原细胞瘤远端区域增加到纯胎盘样碱性磷酸酶阳性的肿瘤区域。重要的是,尽管在梗阻性无精子症患者的生精小管中定位的细胞标记非常弱,但在非梗阻性无精子症的生精小管中,持续存在的生殖细胞、支持细胞和肌样细胞以及纤维组织强烈表达再生 I。这些结果表明,再生 I 可能作为不育症睾丸肿瘤发展的预后标志物。