[The role of plasma chemokines in cancer].

S Struyf, J Van Damme
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引用次数: 0

Abstract

Chemokines have diverse roles in tumor biology. Monocyte chemotactic protein-(MCP-1)/CCL2 was the first chemokine described to elicit influx of monocyte/macrophages into tumors. Application of chemokines as anti-tumoral therapy to attract immunocompetent cells and to mediate the mounting of an efficient anti-tumoral response has been tested as a method to combat cancer for some years now. However, these chemokine-related therapy has not yet been approved for clinical application, although it has been tested succesfully in animal models for years now. A different kind of approach for chemokine anti-cancer therapy involves angiostatic chemokines. These chemokines inhibit pro-angiogenic tumoral factors, thereby limiting tumor growth and metastasis. Recently, we described a most potent new angiostatic chemokine, namely a variant of platelet factor 4, designated PF-4var/CXCL4L1. With regard to hematological tumors we described a new plasma chemokine, PARC/CCL18, that can be used to distinguish between pediatric patients with acute lymfoid leukemia or acute myeloid leukemia. Whether this elevated plasma concentration of PARC/CCL18 is the cause of the pathology or the consequence of a disturbed cytokine balance is not clear at the moment.

血浆趋化因子在癌症中的作用。
趋化因子在肿瘤生物学中具有多种作用。单核细胞趋化蛋白-(MCP-1)/CCL2是第一个被描述引起单核细胞/巨噬细胞流入肿瘤的趋化因子。应用趋化因子作为抗肿瘤治疗来吸引免疫活性细胞并介导有效的抗肿瘤反应,作为一种对抗癌症的方法已经被测试了几年。然而,这些趋化因子相关的治疗尚未被批准用于临床应用,尽管它已经在动物模型中成功地测试了多年。一种不同的趋化因子抗癌治疗方法涉及血管抑制趋化因子。这些趋化因子抑制促血管生成肿瘤因子,从而限制肿瘤生长和转移。最近,我们描述了一种最有效的新的血管抑制趋化因子,即血小板因子4的一种变体,命名为PF-4var/CXCL4L1。关于血液肿瘤,我们描述了一种新的血浆趋化因子,PARC/CCL18,可用于区分急性淋巴样白血病或急性髓性白血病的儿科患者。血浆中PARC/CCL18浓度升高是病理的原因还是细胞因子平衡紊乱的结果,目前尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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