Akram Sura, Al-Shammari Ahmed Majeed, Sahib Hayder B, Jabir Majid Sakhi
Department of Pharmacology, College of Medicine, Al-Nahrain University, Baghdad, Iraq.
Experimental Therapy, Iraqi Center for Cancer and Medical Genetics Research, Mustansiriyah University, Baghdad, Iraq.
Int J Microbiol. 2023 Sep 8;2023:3324247. doi: 10.1155/2023/3324247. eCollection 2023.
Breast cancer is a lethal disease in females worldwide and needs effective treatment. Targeting cancer cells with selective and safe treatment seems like the best choice, as most chemotherapeutic drugs act unselectively. Papaverine showed promising antitumor activity with a high safety profile and increased blood flow through vasodilation. At the same time, it was widely noticed that virotherapy using the Newcastle disease virus proved to be safe and selective against a broad range of cancer cells. Furthermore, combination therapy is favorable, as it attacks cancer cells with multiple mechanisms and enhances virus entrance into the tumor mass, overcoming cancer cells' resistance to therapy. Therefore, we aimed at assessing the novel combination of the AMHA1 strain of Newcastle disease virus (NDV) and nonnarcotic opium alkaloid (papaverine) against breast cancer models in vitro and in vivo. In vitro experiments used two human breast cancer cell lines and one normal cell line and were treated with NDV, papaverine, and a combination. The study included a cell viability MTT assay, morphological analysis, and apoptosis detection. Animal experiments used the AN3 mouse mammary adenocarcinoma tumor model. Evaluation of the antitumor activity included growth inhibition measurement; the immunohistochemistry assay measured caspase protein expression. Finally, a semiquantitative microarray assay was used to screen changes in apoptotic proteins. In vitro, results showed that the combination therapy induces synergistic cytotoxicity and apoptosis against cancer cells with a negligible cytotoxic effect on normal cells. In vivo, combination treatment induced a significant antitumor effect with an obvious regression in tumor size and a remarkable and significant expression of caspase-3, caspase-8, and caspase-9 compared to monotherapies. Microarray analysis shows higher apoptosis protein levels in the combination therapy group. In conclusion, this study demonstrated the role of papaverine in enhancing the antitumor activity of NDV, suggesting a promising strategy for breast cancer therapy through nonchemotherapeutic drugs.
乳腺癌是全球女性中的致命疾病,需要有效的治疗方法。由于大多数化疗药物作用无选择性,因此用选择性且安全的治疗方法靶向癌细胞似乎是最佳选择。罂粟碱显示出有前景的抗肿瘤活性,安全性高,且通过血管舒张增加血流量。同时,人们广泛注意到,使用新城疫病毒的病毒疗法被证明对多种癌细胞安全且具有选择性。此外,联合治疗是有利的,因为它通过多种机制攻击癌细胞,并增强病毒进入肿瘤块,克服癌细胞对治疗的抗性。因此,我们旨在评估新城疫病毒(NDV)的AMHA1株与非麻醉性鸦片生物碱(罂粟碱)对体外和体内乳腺癌模型的新型联合作用。体外实验使用了两个人类乳腺癌细胞系和一个正常细胞系,并用NDV、罂粟碱及其组合进行处理。该研究包括细胞活力MTT测定、形态学分析和凋亡检测。动物实验使用AN3小鼠乳腺腺癌肿瘤模型。抗肿瘤活性评估包括生长抑制测量;免疫组织化学测定法测量半胱天冬酶蛋白表达。最后,使用半定量微阵列测定法筛选凋亡蛋白的变化。在体外,结果表明联合治疗对癌细胞诱导协同细胞毒性和凋亡,对正常细胞的细胞毒性可忽略不计。在体内,联合治疗诱导显著的抗肿瘤作用,肿瘤大小明显缩小,与单一疗法相比,半胱天冬酶-3、半胱天冬酶-8和半胱天冬酶-9有显著且明显的表达。微阵列分析显示联合治疗组中凋亡蛋白水平更高。总之,本研究证明了罂粟碱在增强NDV抗肿瘤活性中的作用,提示通过非化疗药物治疗乳腺癌的一种有前景的策略。