Majewski S, Szmurlo A, Marczak M, Jablonska S, Bollag W
Department of Dermatology, Warsaw School of Medicine, Poland.
Int J Cancer. 1994 Apr 1;57(1):81-5. doi: 10.1002/ijc.2910570115.
Various retinoids and interferons exert anti-tumor effects both in experimental studies and in clinical trials. Recent reports indicate that they have a synergistic antineoplastic activity. Our study aimed to determine whether these synergistic anti-tumor effects are related to inhibition of tumor-cell-induced angiogenesis. A further aim was to compare the anti-angiogenic activity of various retinoids including 9-cis retinoic acid, a ligand for nuclear retinoic acid receptor RXR, given alone and in combination with interferon alpha-2a (IFN alpha-2a). An in vivo experimental model of cutaneous angiogenesis in the mouse was used. Angiogenesis was induced by intradermal injection of HPV16- or HPV18 DNA-harboring tumor-cell lines. All-trans retinoic acid (all-trans RA), 13-cis retinoic acid (13-cis RA) and 9-cis retinoic acid (9-cis RA) as well as IFN alpha-2a applied to mice intraperitoneally for 5 consecutive days before induction of angiogenesis resulted in significant inhibition of angiogenesis. Combination of retinoids with IFN alpha-2a led to a synergistic inhibition of angiogenesis, as compared to the effects of the drugs given alone. Similar results were obtained when tumor cells were preincubated in vitro with the compounds, before injection into untreated mice. Our findings on synergistic anti-angiogenic effects of retinoids and IFN alpha-2a could explain, at least partially, the anti-tumor efficacy of combined therapy with these agents, and provide support for the role of angiogenesis in tumor growth.
多种维甲酸和干扰素在实验研究和临床试验中均发挥抗肿瘤作用。最近的报告表明,它们具有协同抗肿瘤活性。我们的研究旨在确定这些协同抗肿瘤作用是否与抑制肿瘤细胞诱导的血管生成有关。另一个目的是比较各种维甲酸的抗血管生成活性,包括9-顺式维甲酸(一种核维甲酸受体RXR的配体)单独使用以及与α-2a干扰素(IFNα-2a)联合使用时的情况。采用了小鼠皮肤血管生成的体内实验模型。通过皮内注射携带HPV16或HPV18 DNA的肿瘤细胞系来诱导血管生成。在诱导血管生成前连续5天腹腔内给小鼠施用全反式维甲酸(全反式RA)、13-顺式维甲酸(13-顺式RA)和9-顺式维甲酸(9-顺式RA)以及IFNα-2a,可显著抑制血管生成。与单独给药的效果相比,维甲酸与IFNα-2a联合使用可导致血管生成受到协同抑制。当肿瘤细胞在体外与这些化合物预孵育后再注射到未处理的小鼠体内时,也获得了类似的结果。我们关于维甲酸和IFNα-2a协同抗血管生成作用的发现至少可以部分解释这些药物联合治疗的抗肿瘤疗效,并为血管生成在肿瘤生长中的作用提供支持。