Rosas Carlos, Sinning Mariana, Ferreira Arturo, Fuenzalida Marcela, Lemus David
Biol Res. 2014 Jun 16;47(1):27. doi: 10.1186/0717-6287-47-27.
During the last few years it has been shown in several laboratories that Celecoxib (Cx), a non-steroidal anti-inflammatory agent (NSAID) normally used for pain and arthritis, mediates antitumor and antiangiogenic effects. However, the effects of this drug on a tumor cell line resistant to chemotherapeutical drugs used in cancer have not been described.
Cx reduces angiogenesis in the chick embryonic chorioallantoic membrane assay (CAM), inhibits the growth and microvascular density of the murine TA3-MTXR tumor, reduces microvascular density of tumor metastases, promotes apoptosis and reduces vascular endothelial growth factor (VEGF) production and cell proliferation in the tumor.
The antiangiogenic and antitumor Cx effects correlate with its activity on other tumor cell lines, suggesting that Prostaglandins (PGs) and VEGF production are involved. These results open the possibility of using Celecoxib combined with other experimental therapies, ideally aiming to get synergic effects.
在过去几年中,多个实验室已表明,塞来昔布(Cx),一种通常用于止痛和治疗关节炎的非甾体抗炎药(NSAID),具有介导抗肿瘤和抗血管生成的作用。然而,该药物对癌症中使用的化疗药物耐药的肿瘤细胞系的影响尚未见报道。
在鸡胚绒毛尿囊膜试验(CAM)中,Cx可减少血管生成,抑制小鼠TA3 - MTXR肿瘤的生长和微血管密度,降低肿瘤转移灶的微血管密度,促进细胞凋亡,并减少肿瘤中血管内皮生长因子(VEGF)的产生和细胞增殖。
Cx的抗血管生成和抗肿瘤作用与其对其他肿瘤细胞系的活性相关,提示前列腺素(PGs)和VEGF的产生参与其中。这些结果为联合使用塞来昔布与其他实验性疗法提供了可能性,理想情况下旨在获得协同效应。