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类视黄醇、1,25-二羟基维生素D3及其组合对肿瘤细胞诱导的血管生成的抑制作用。

Inhibition of tumor cell-induced angiogenesis by retinoids, 1,25-dihydroxyvitamin D3 and their combination.

作者信息

Majewski S, Szmurlo A, Marczak M, Jablonska S, Bollag W

机构信息

Department of Dermatology, Warsaw School of Medicine, Poland.

出版信息

Cancer Lett. 1993 Nov 30;75(1):35-9. doi: 10.1016/0304-3835(93)90204-m.

Abstract

Tumor-induced angiogenesis (TIA), i.e., the ability of transformed cells to stimulate new blood vessel formation is an important factor contributing to tumor growth and invasiveness. The antiangiogenic effect of the retinoids, all-trans retinoic acid, 13-cis retinoic and 9-cis retinoic acid, of 1,25-dihydroxyvitamin D3, and of their combinations were studied using an experimental system in vivo. TIA was induced in immunosuppressed mice by intradermal injection of the two human transformed keratinocyte lines, Skv-e2, harboring DNA of human papillomavirus (HPV) type 16, and HeLa, harboring HPV18 DNA. The three retinoids and 1,25-dihydroxyvitamin D3, when administered systemically to mice, before the angiogenesis assay significantly decreased TIA. Their combination led to a synergistic inhibition of TIA. These results provide the basis for the use of combination of retinoids and 1,25-dihydroxyvitamin D3 in treatment of neoplastic diseases.

摘要

肿瘤诱导的血管生成(TIA),即转化细胞刺激新血管形成的能力,是促进肿瘤生长和侵袭的一个重要因素。使用体内实验系统研究了视黄酸、全反式维甲酸、13-顺式维甲酸和9-顺式维甲酸、1,25-二羟基维生素D3及其组合的抗血管生成作用。通过皮内注射两种携带人乳头瘤病毒(HPV)16型DNA的人转化角质形成细胞系Skv-e2和携带HPV18 DNA的HeLa细胞系,在免疫抑制小鼠中诱导TIA。在血管生成测定之前,将这三种视黄酸和1,25-二羟基维生素D3全身给药于小鼠,可显著降低TIA。它们的组合导致对TIA的协同抑制。这些结果为视黄酸和1,25-二羟基维生素D3联合用于治疗肿瘤性疾病提供了依据。

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