Potensi Kombinasi Adenosine Diphosphate-Ribosylation Like 4c Antisense Oligonuclotide-1316 dengan Polyamidoamine Dendrimer Generasi 4-Anti Surfactant Protein B sebagai Terapi Adenokarsinoma Paru

Adrian Wiryanata Gorintha, Andrea Ivena, Putu Aprilyanti Aristadewi, Agung Wiwiek Indrayani
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Abstract

Background: Lung cancer is a disease of the respiratory system that gets special attention because the World Health Organization (WHO) has reported that in 2018, lung cancer was the cancer with the highest number of morbidity and mortality rate in the world. There are several types of lung cancer, one of which is adenocarcinoma, which accounts for about 40% of all lung cancers. In its management, cancer cells often develop resistance to EGFR TKI drugs while Cisplatin and Crizotinib have quite dangerous side effects, namely bradycardia to cardiotoxicity.Methods: The method used is a literature review with literature sources in the form of relevant article from search engine such as Pubmed and Google Scholar that contain keyword “ARL4C ASO-1316”, “lung adenocarcinoma”, “PAMAM Dendrimer Generasi 4” and “anti SFTPB antibody”.Result: The ability of ARL4C ASO-1316 in inhibiting the division and migration of lung adenocarcinoma cells has been proven in vivo and in vitro so that it can provide hope in the form of new modalities in the treatment of lung adenocarcinoma. In addition, the combination with the PAMAM Dendrimer G4-Anti SFTPB carrier can increase the ability to deliver ARL4C ASO-1316 to reach target tissues rapidly and can provide maximum effect in the treatment of lung adenocarcinoma.Conclusion : Adenosine diphosphate-ribosylation like 4c antisense oligonuclotide-1316 with polyamidoamine dendrimer generation 4-anti surfactant protein b should provide novel approaches and new insights for lung adenocarcinoma.
背景:肺癌是一种受到特别关注的呼吸系统疾病,因为世界卫生组织(WHO)报告称,2018年肺癌是全球发病率和死亡率最高的癌症。肺癌有几种类型,其中一种是腺癌,约占所有肺癌的40%。在治疗过程中,癌细胞经常对EGFR TKI药物产生耐药性,而顺铂和克唑替尼具有相当危险的副作用,即心动过缓到心脏毒性。方法:采用文献综述法,文献来源为Pubmed、Google Scholar等搜索引擎上的相关文章,包含关键词“ARL4C ASO-1316”、“肺腺癌”、“PAMAM Dendrimer Generasi 4”、“anti SFTPB antibody”。结果:ARL4C ASO-1316对肺腺癌细胞分裂和迁移的抑制作用已在体内和体外得到证实,为肺腺癌的治疗提供了新的模式。此外,与PAMAM Dendrimer G4-Anti SFTPB载体联合可增加ARL4C ASO-1316快速递送至靶组织的能力,在肺腺癌的治疗中可提供最大的效果。结论:二磷酸腺苷-核糖基化样4c反义寡核苷酸-1316与聚胺胺树突状物第4代抗表面活性剂蛋白b可能为肺腺癌的治疗提供新途径和新见解。
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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