Department of Chemical Engineering, University of Massachusetts Amherst, MA 01003, USA.
Molecular and Cellular Biology Graduate Program, University of Massachusetts Amherst, MA 01003, USA.
Sci Adv. 2024 Mar 8;10(10):eadl0165. doi: 10.1126/sciadv.adl0165.
Dormant, disseminated breast cancer cells resist treatment and may relapse into malignant metastases after decades of quiescence. Identifying how and why these dormant breast cancer cells are triggered into outgrowth is a key unsolved step in treating latent, metastatic breast cancer. However, our understanding of breast cancer dormancy in vivo is limited by technical challenges and ethical concerns with triggering the activation of dormant breast cancer. In vitro models avoid many of these challenges by simulating breast cancer dormancy and activation in well-controlled, bench-top conditions, creating opportunities for fundamental insights into breast cancer biology that complement what can be achieved through animal and clinical studies. In this review, we address clinical and preclinical approaches to treating breast cancer dormancy, how precisely controlled artificial environments reveal key interactions that regulate breast cancer dormancy, and how future generations of biomaterials could answer further questions about breast cancer dormancy.
休眠的、播散的乳腺癌细胞抵抗治疗,并在数十年的静止后可能复发为恶性转移。确定这些休眠的乳腺癌细胞如何以及为何被触发生长是治疗潜伏性、转移性乳腺癌的一个关键未解决步骤。然而,我们对体内乳腺癌休眠的理解受到技术挑战和触发休眠乳腺癌激活的伦理问题的限制。体外模型通过在良好控制的台式条件下模拟乳腺癌休眠和激活来避免许多这些挑战,为深入了解乳腺癌生物学提供了机会,这些机会补充了通过动物和临床研究可以实现的机会。在这篇综述中,我们讨论了治疗乳腺癌休眠的临床和临床前方法,精确控制的人工环境如何揭示调节乳腺癌休眠的关键相互作用,以及未来几代生物材料如何进一步回答关于乳腺癌休眠的问题。