Department of Oncology, Aarhus University Hospital, Aarhus C, Denmark.
Division of Oncology and Pathology, Lund University, Lund, Sweden.
J Intern Med. 2018 Oct;284(4):346-357. doi: 10.1111/joim.12806. Epub 2018 Jul 9.
Statin drugs have been used for more than two decades to treat hypercholesterolemia and as cardio-preventive drugs, resulting in a marked decrease in cardiovascular morbidity and mortality worldwide. Statins halt hepatic cholesterol biosynthesis by inhibiting the rate-limiting enzyme in the mevalonate pathway, hydroxymethylglutaryl-coenzyme A reductase (HMGCR). The mevalonate pathway regulates a host of biochemical processes in addition to cholesterol production. Attenuation of these pathways is likely responsible for the myriad benefits of statin therapy beyond cholesterol reduction - the so-called pleiotropic effects of statins. Chief amongst these purported effects is anti-cancer activity. A considerable body of preclinical, epidemiologic and clinical evidence shows that statins impair proliferation of breast cancer cells and reduce the risk of breast cancer recurrence. Potential mechanisms for this effect have been explored in laboratory models, but remain poorly understood and require further investigation. The number of clinical trials assessing the putative clinical benefit of statins in breast cancer is increasing. Currently, a total of 30 breast cancer/statin trials are listed at the global trial identifier website clinicaltrials.gov. Given the compelling evidence from performed trials in a variety of clinical settings, there have been calls for a clinical trial of statins in the adjuvant breast cancer setting. It would be imperative for such a trial to incorporate tumour biomarkers predictive of statin response in its design and analysis plan. Ongoing translational clinical trials aimed at biomarker discovery will help identify, which breast cancer patients are most likely to benefit from adjuvant statin therapy, and will add valuable clinical knowledge to the field.
他汀类药物已被用于治疗高胆固醇血症和预防心血管疾病超过 20 年,在全球范围内显著降低了心血管疾病的发病率和死亡率。他汀类药物通过抑制甲羟戊酸途径中的限速酶羟甲基戊二酰辅酶 A 还原酶(HMGCR)来阻止肝脏胆固醇的生物合成。甲羟戊酸途径除了调节胆固醇的产生外,还调节着许多生化过程。这些途径的衰减可能是他汀类药物治疗除了降低胆固醇之外的众多益处的原因,即所谓的他汀类药物的多效性作用。其中最重要的作用之一是抗癌活性。大量的临床前、流行病学和临床证据表明,他汀类药物可抑制乳腺癌细胞的增殖,并降低乳腺癌复发的风险。在实验室模型中已经探索了这种作用的潜在机制,但仍了解甚少,需要进一步研究。评估他汀类药物在乳腺癌中潜在临床获益的临床试验数量正在增加。目前,在全球试验标识符网站 clinicaltrials.gov 上共列出了 30 项乳腺癌/他汀类药物试验。鉴于在各种临床环境中进行的试验所提供的令人信服的证据,人们呼吁在辅助乳腺癌环境中进行他汀类药物的临床试验。对于这样的试验,至关重要的是在其设计和分析计划中纳入预测他汀类药物反应的肿瘤生物标志物。正在进行的旨在发现生物标志物的转化临床试验将有助于确定哪些乳腺癌患者最有可能从辅助他汀类药物治疗中获益,并为该领域增加宝贵的临床知识。