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尿激酶型纤溶酶原激活剂基因Pro141Leu多态性与前列腺癌患者的关系。

The relationship between the urokinase-type plasminogen activator gene Pro141Leu polymorphism and patients with prostate cancer.

作者信息

Gülüm Cemil, Eroğlu Pelin, Tanrıverdi Rojda, Bozlu Murat

机构信息

Mersin University, Faculty of Science, Department of Chemistry - Mersin, Turkey.

Mersin University, Faculty of Medicine, Department of Biochemistry - Mersin, Turkey.

出版信息

Rev Assoc Med Bras (1992). 2025 Aug 8;71(7):e20250097. doi: 10.1590/1806-9282.20250097. eCollection 2025.

Abstract

OBJECTIVE

Although many genes associated with prostate cancer have been identified, there are still many cases of prostate cancer whose genetics have not been identified. The urokinase-type plasminogen activator gene is thought to play a key role in cancer invasion and metastasis. The Pro141Leu polymorphism may be involved in the development of prostate cancer, although genetic evidence is lacking.

METHODS

We used the real time polymerase chain reaction based TaqMan assay to investigate whether the urokinase-type plasminogen activator gene Pro141Leu polymorphism is associated with prostate cancer patients and healthy controls. urokinase-type plasminogen activator, urokinase-type plasminogen activator receptor, and prostate-specific antigen antigens were assayed by the enzyme-linked immunosorbent assay method.

RESULTS

We found no significant differences between the cancer and control populations in terms of genotype distribution (CC, CT, and TT). Furthermore, we found no association between the urokinase-type plasminogen activator gene Pro141Leu polymorphism and cancer risk in prostate cancer patients.

CONCLUSION

This is the first study to investigate the association between the rs2227564 polymorphism and prostate cancer. Although the urokinase-type plasminogen activator gene Pro141Leu polymorphism has been reported to be a risk factor for some cancers, our findings suggest that the urokinase-type plasminogen activator gene Pro141Leu polymorphism is not an important genetic risk factor for prostate cancer.

摘要

目的

尽管已经鉴定出许多与前列腺癌相关的基因,但仍有许多前列腺癌病例的遗传学特征尚未明确。尿激酶型纤溶酶原激活剂基因被认为在癌症侵袭和转移中起关键作用。尽管缺乏遗传学证据,但Pro141Leu多态性可能与前列腺癌的发生有关。

方法

我们使用基于实时聚合酶链反应的TaqMan分析法,研究尿激酶型纤溶酶原激活剂基因Pro141Leu多态性是否与前列腺癌患者和健康对照相关。采用酶联免疫吸附测定法检测尿激酶型纤溶酶原激活剂、尿激酶型纤溶酶原激活剂受体和前列腺特异性抗原。

结果

我们发现癌症患者和对照组在基因型分布(CC、CT和TT)方面没有显著差异。此外,我们发现尿激酶型纤溶酶原激活剂基因Pro141Leu多态性与前列腺癌患者的癌症风险之间没有关联。

结论

这是第一项研究rs2227564多态性与前列腺癌之间关联的研究。尽管尿激酶型纤溶酶原激活剂基因Pro141Leu多态性已被报道为某些癌症的危险因素,但我们的研究结果表明,尿激酶型纤溶酶原激活剂基因Pro141Leu多态性不是前列腺癌的重要遗传危险因素。

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