{"title":"Research question: A comparison of Fluorouracil and Docetaxel in the treatment of gastric cancer","authors":"Junteng Pan","doi":"10.54254/2753-8818/45/20240514","DOIUrl":null,"url":null,"abstract":"Cancer is a serious lethal disease that is prevalent worldwide. This disease is mainly due to the development of abnormal cells that divide without any control. These abnormal cells, also known as tumor cells, can destroy normal body tissue. Causing numerous deaths around the world. Gastric cancer, commonly known as stomach cancer, is the cancer to be discussed in depth in this essay. It is one of the most prevalent and lethal cancers worldwide. Its cases and mortality rates vary significantly across different regions, reflecting differences in diet, genetics, and medicine access. Gastric cancer presents substantial challenges in medical treatment. The disease's complexity also leads to the exploration of various treatment methods. Among many pharmacological options, Fluorouracil and Docetaxel are two significant medicines that are worth discussing in depth. Fluorouracil and Docetaxel are both used in chemotherapy. However, they have distinct mechanisms and properties. Fluorouracil is a pyrimidine analog used to inhibit DNA synthesis of cancerous cells, while Docetaxel is a taxane that targets microtubules. They all played a vital role in treating cancer. Nevertheless, their comparative effectiveness and safety remain in debate. This essay aims to provide a depth comparison of Fluorouracil and Docetaxel. Focusing on their chemical structure, mechanisms of action, delivery modes, resistance, and toxicity, in the treatment of gastric cancer. Offering a better comprehension of two drugs, which are used for their optimal use in patient care.","PeriodicalId":341023,"journal":{"name":"Theoretical and Natural Science","volume":"25 7","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Theoretical and Natural Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.54254/2753-8818/45/20240514","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Cancer is a serious lethal disease that is prevalent worldwide. This disease is mainly due to the development of abnormal cells that divide without any control. These abnormal cells, also known as tumor cells, can destroy normal body tissue. Causing numerous deaths around the world. Gastric cancer, commonly known as stomach cancer, is the cancer to be discussed in depth in this essay. It is one of the most prevalent and lethal cancers worldwide. Its cases and mortality rates vary significantly across different regions, reflecting differences in diet, genetics, and medicine access. Gastric cancer presents substantial challenges in medical treatment. The disease's complexity also leads to the exploration of various treatment methods. Among many pharmacological options, Fluorouracil and Docetaxel are two significant medicines that are worth discussing in depth. Fluorouracil and Docetaxel are both used in chemotherapy. However, they have distinct mechanisms and properties. Fluorouracil is a pyrimidine analog used to inhibit DNA synthesis of cancerous cells, while Docetaxel is a taxane that targets microtubules. They all played a vital role in treating cancer. Nevertheless, their comparative effectiveness and safety remain in debate. This essay aims to provide a depth comparison of Fluorouracil and Docetaxel. Focusing on their chemical structure, mechanisms of action, delivery modes, resistance, and toxicity, in the treatment of gastric cancer. Offering a better comprehension of two drugs, which are used for their optimal use in patient care.
癌症是一种严重的致命疾病,在全球范围内普遍存在。这种疾病主要是由于异常细胞不受控制地分裂发展而成。这些异常细胞又称肿瘤细胞,会破坏正常的身体组织。导致世界各地无数人死亡。胃癌,俗称胃癌,是本文要深入讨论的癌症。它是全球发病率最高、致死率最高的癌症之一。不同地区的病例和死亡率差异很大,反映了饮食、遗传和医疗条件的差异。胃癌给医疗带来了巨大挑战。这种疾病的复杂性也促使人们探索各种治疗方法。在众多药物治疗方案中,氟尿嘧啶和多西他赛是值得深入探讨的两种重要药物。氟尿嘧啶和多西他赛都是化疗药物。不过,它们具有不同的机制和特性。氟尿嘧啶是一种嘧啶类似物,用于抑制癌细胞的 DNA 合成,而多西他赛则是一种针对微管的类固醇。它们在治疗癌症方面都发挥了重要作用。然而,它们的有效性和安全性比较仍存在争议。本文旨在对氟尿嘧啶和多西他赛进行深入比较。重点介绍它们在治疗胃癌方面的化学结构、作用机制、给药模式、耐药性和毒性。让人们更好地理解这两种药物在患者治疗中的最佳应用。