Effect of LHS-1269 on morphology and angiogenesis of Lewis lung carcinoma

I. B. Merkulova, I. Golubeva, D. Khochenkov, T. V. Abramova, N. Ermakova, L. V. Ektova
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Abstract

Background. The new anticancer chemical compound LHS-1269 from the class of indolocarbazoles is undergoing preclinical studies at the N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia. LHS-1269 has a high antitumor activity on transplanted tumors of mice, showed high cytotoxic activity on many tumor cells lines in vitro, and has shown an inhibitory effect on vasculogenic mimicry in tumors in vitro. LHS-1269 does not affect the catalytic activity of human topoisomerases I and IIα. An antiangiogenic mechanism of the drug’s antitumor action is suggested.Aim. To evaluate the effect of LHS-1269 on the morphological features and angiogenesis of transplanted Lewis lung carcinoma (LLC) in BDF1 mice.Materials and methods. In BDF1 mice (n = 20) with transplanted LLC tumor on days 1 and 3 after 5-fold intraperitoneal administration of LHS-1269 in a single dose of 60 mg (total dose – 300 mg/kg), mice (n = 20) on days 5 and 8 after a single intravenous injection of LHS-1269 at a dose of 100 mg/kg, mice (n = 20) with transplanted LLC tumor without administration of LHS-1269 (control). The assessment of the antitumor effect was carried out according to the criterion of inhibition of tumor growth (%) and the study of the morphological features of the tumors. To assess the effect of LHS-1269 on tumor angiogenesis in LLC tumor sections, a visual calculation of the average number (density) of blood vessels and immunohistochemical detection of expression of the CD31+ endothelial marker were performed.Results. The LHS-1269 compound in animal groups with 5-fold and 1-fold use caused tumor growth inhibition – 59–70 and 67–79 %, with pronounced morphological changes and tumor cell death. There is an uneven distribution of blood vessels in tumors and surrounding tissues in all groups. LHS-1269 caused a statistically significant decrease in the average number of blood vessels in the tumor both after 5-fold and after 1-fold administration. The statistically significant decrease in the average number of blood vessels in the surrounding connective tissue tumor was observed only after 5-fold administration of the drug. The decrease in the average number of CD31+ endothelial cells after five times intraperitoneal administration was statistically insignificant compared to control (83.1 ± 8.7 and 59.6 ± 18.9, respectively). The increase in this indicator after a single intravenous injection of LHS-1269 was statistically significant.Conclusion. LHS-1269, when administered five times and once in mice, caused pronounced morphological changes in the form of damage and death of LLC tumor cells. The results of a study of angiogenesis in a tumor do not allow an unambiguous conclusion about the inhibitory effect of LHS-1269 on angiogenesis in LLC tumors in mice.
LHS-1269对Lewis肺癌形态学及血管生成的影响
背景。来自吲哚咔唑类的新型抗癌化合物LHS-1269正在俄罗斯卫生部N.N. Blokhin国家肿瘤医学研究中心进行临床前研究。LHS-1269对小鼠移植肿瘤具有较高的抗肿瘤活性,在体外对多种肿瘤细胞系显示出较高的细胞毒活性,并在体外对肿瘤血管生成模拟表现出抑制作用。LHS-1269不影响人拓扑异构酶I和Iα的催化活性。提出了该药抗肿瘤作用的抗血管生成机制。探讨LHS-1269对BDF1小鼠移植Lewis肺癌(LLC)形态学特征及血管生成的影响。材料和方法。LHS-1269单次给药60 mg(总剂量为300 mg/kg), 5次腹腔注射LHS-1269单次给药100 mg/kg后,第1天和第3天,移植LLC肿瘤的BDF1小鼠(n = 20),移植LLC肿瘤的小鼠(n = 20),不给药LHS-1269作为对照。根据抑制肿瘤生长(%)的标准和肿瘤形态学特征的研究进行抗肿瘤效果的评价。为了评估LHS-1269对LLC肿瘤切片血管生成的影响,我们通过视觉计算血管的平均数量(密度)和免疫组化检测CD31+内皮标志物的表达。LHS-1269化合物在5倍和1倍使用的动物组中,肿瘤生长抑制率分别为59-70和67-79 %,并出现明显的形态改变和肿瘤细胞死亡。各组肿瘤及周围组织血管分布不均匀。LHS-1269给药5倍和1倍后,肿瘤平均血管数均有统计学意义的减少。仅在5倍给药后,结缔组织肿瘤周围的平均血管数才有统计学意义的减少。5次腹腔给药后CD31+内皮细胞的平均数量较对照组减少(分别为83.1±8.7和59.6±18.9),差异无统计学意义。单次静脉注射LHS-1269后,该指标升高有统计学意义。LHS-1269给药五次和一次小鼠,引起LLC肿瘤细胞损伤和死亡的明显形态学改变。一项肿瘤血管生成的研究结果不能明确地得出LHS-1269对小鼠LLC肿瘤血管生成的抑制作用。
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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