Struyf S, Van Damme J
Laboratorium voor Moleculaire Immunologie, Rega Instituut, KULeuve, Minderbroedersstraat 10, B 3000, Leuven.
Verh K Acad Geneeskd Belg. 2007;69(3):149-65.
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.
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 -1(MCP -1)/CCL2是首个被描述可促使单核细胞/巨噬细胞流入肿瘤的趋化因子。将趋化因子作为抗肿瘤疗法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多年。然而,尽管这些趋化因子相关疗法多年来在动物模型中测试成功,但尚未被批准用于临床应用。趋化因子抗癌疗法的另一种不同方法涉及血管生成抑制趋化因子。这些趋化因子抑制促血管生成的肿瘤因子,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型血管生成抑制趋化因子,即血小板因子4的一个变体,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,它可用于区分患有急性淋巴细胞白血病或急性髓细胞白血病的儿科患者。目前尚不清楚PARC/CCL18血浆浓度升高是病理原因还是细胞因子平衡紊乱的结果。