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激肽释放酶相关肽酶在人类恶性肿瘤中的预后价值和生物学作用。

Prognostic value and biological role of the kallikrein-related peptidases in human malignancies.

机构信息

Department of Biochemistry & Molecular Biology, University of Athens, Athens, Greece.

出版信息

Future Oncol. 2010 Feb;6(2):269-85. doi: 10.2217/fon.09.149.

Abstract

Cancer is a substantial health problem for the populations of the Western world. The discovery of new molecular biomarkers for diagnosis, prognosis and monitoring patients' response to therapy can aid in combating this complicated disease. The human kallikrein-related peptidases (human tissue kallikreins [KLKs]) are encoded by a continuous multigene family, located on chromosomal region 19q13.3-4. KLK3 (prostate-specific antigen) is the most efficient cancer biomarker ever employed. KLK genes are expressed abnormally in various malignancies, where they affect cancer-cell growth and metastasis. Their deregulated expression pattern, often associated with various clinicopathological characteristics of cancer patients, can be exploited, solely or within multiparametric panels, as a prognostic biomarker. Recent data illustrate that discernible molecular modulations of KLKs, occurring as a result of cancer cells' treatment with antitumor agents, may serve as new potential biomarkers, possibly predicting patients' treatment response. It is believed that KLKs might be employed in future clinical practice as novel and effective tumor markers.

摘要

癌症是西方世界人口面临的一个重大健康问题。发现新的分子生物标志物用于诊断、预后和监测患者对治疗的反应,可以帮助对抗这种复杂的疾病。人类激肽释放酶相关肽酶(人组织激肽释放酶[KLKs])由位于染色体 19q13.3-4 区域上的连续多基因家族编码。KLK3(前列腺特异性抗原)是迄今为止使用的最有效的癌症生物标志物。KLK 基因在各种恶性肿瘤中异常表达,影响癌细胞的生长和转移。它们的表达失调模式通常与癌症患者的各种临床病理特征相关,可以单独或在多参数面板中用作预后生物标志物。最近的数据表明,由于癌细胞接受抗肿瘤药物治疗而导致的 KLKs 的明显分子调节,可能作为新的潜在生物标志物,预测患者的治疗反应。人们相信 KLKs 可能在未来的临床实践中作为新型有效的肿瘤标志物得到应用。

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