Institute of Cancer Medicine, The University of Liverpool, UK.
Institute of Cancer Medicine, The University of Liverpool, UK.
Surg Oncol. 2020 Jun;33:100-107. doi: 10.1016/j.suronc.2020.02.006. Epub 2020 Feb 11.
Tamoxifen is a widely used hormonal based therapy for breast cancer in the adjuvant and metastatic setting, prolonging overall and recurrence-free survival. There has been increasing interest in the potential for novel "off-target" effects of tamoxifen and its metabolite N-desmethyltamoxifen across a number of cancer types. We aim to review the current literature regarding the potential use of tamoxifen in other primary malignancies.
A qualitative systematic review was performed according to the PRISMA guidelines using pre-set search criteria across the PubMed, Cochrane and Scopus databases from 1985 to 2019. Additional results were generated from included papers references.
A total of 324 papers were identified, of which 47 were included; a further 29 articles were obtained from additional referencing to give a total of 76 articles. Clinical trials have demonstrated benefits with the use of tamoxifen in isolation and combination, specifically in patients with advanced non-resectable malignancy, however results are not consistent across the literature. In vivo data consistently suggests that off target effects of tamoxifen are mediated through the ceramide pathway or through inhibition of protein kinase C (PKC).
With increased focus upon the potential of repurposing drugs, tamoxifen may be a candidate for repurposing in the wider cancer setting. There is evidence to suggest that the ceramide or PKC pathway could act as a therapeutic target for tamoxifen or alternative chemotherapeutics and merits further investigation.
他莫昔芬是一种广泛应用于乳腺癌辅助和转移性治疗的激素治疗药物,可延长总生存期和无复发生存期。人们对他莫昔芬及其代谢物 N-去甲基他莫昔芬在多种癌症类型中潜在的“非靶点”作用越来越感兴趣。我们旨在综述他莫昔芬在其他原发性恶性肿瘤中潜在应用的相关文献。
根据 PRISMA 指南,我们使用预设定的搜索标准,对从 1985 年到 2019 年的 PubMed、Cochrane 和 Scopus 数据库进行了定性系统评价。还从纳入的文献参考文献中生成了额外的结果。
共确定了 324 篇论文,其中 47 篇被纳入;从额外的参考文献中又获得了 29 篇文章,总计 76 篇文章。临床试验表明,他莫昔芬单独使用和联合使用都能使患有晚期不可切除恶性肿瘤的患者获益,但文献结果并不一致。体内数据一致表明,他莫昔芬的非靶点作用是通过神经酰胺途径或通过抑制蛋白激酶 C(PKC)介导的。
随着人们越来越关注重新利用药物的潜力,他莫昔芬可能成为重新应用于更广泛的癌症治疗的候选药物。有证据表明,神经酰胺或 PKC 途径可能成为他莫昔芬或其他化疗药物的治疗靶点,值得进一步研究。