Department of Immunotherapeutics and Biotechnology, and Center for Tumor Immunology and Targeted Cancer Therapy, Texas Tech University Health Sciences Center, Abilene, TX 79601, USA.
Department of Immunotherapeutics and Biotechnology, and Center for Tumor Immunology and Targeted Cancer Therapy, Texas Tech University Health Sciences Center, Abilene, TX 79601, USA.
Biochim Biophys Acta Mol Basis Dis. 2020 Apr 1;1866(4):165424. doi: 10.1016/j.bbadis.2019.02.019. Epub 2019 Feb 26.
Recent advances in research on cancer have led to understand the pathogenesis of cancer and development of new anticancer drugs. Despite of these advancements, many tumors have been found to recur, undergo metastasis and develop resistance to therapy. Accumulated evidences suggest that small population of cancer cells known as cancer stem cells (CSC) are responsible for reconstitution and propagation of the disease. CSCs possess the ability to self-renew, differentiate and proliferate like normal stem cells. CSCs also appear to have resistance to anti-cancer therapies and subsequent relapse. The underlying stemness properties of the CSCs are reliant on multiple molecular targets such as signaling pathways, cell surface molecules, tumor microenvironment, apoptotic pathways, microRNA, stem cell differentiation, and drug resistance markers. Thus an effective therapeutic strategy relies on targeting CSCs to overcome the possible tumor relapse and chemoresistance. The targeted inhibition of these stem cell biomarkers is one of the promising approaches to eliminate cancer stemness. This review article summarizes possible targets of cancer cell stemness for the complete treatment of cancer.
近年来癌症研究的进展使人们了解了癌症的发病机制和新抗癌药物的开发。尽管取得了这些进展,但仍发现许多肿瘤会复发、转移并对治疗产生耐药性。越来越多的证据表明,一小部分称为癌症干细胞 (CSC) 的癌细胞负责疾病的重建和传播。CSC 具有自我更新、分化和增殖的能力,就像正常干细胞一样。CSC 似乎也对癌症治疗有抗药性,随后会复发。CSC 的这种潜在干细胞特性依赖于多个分子靶点,如信号通路、细胞表面分子、肿瘤微环境、凋亡途径、microRNA、干细胞分化和耐药性标志物。因此,有效的治疗策略依赖于针对 CSC 以克服可能的肿瘤复发和化疗耐药性。靶向这些干细胞生物标志物的抑制是消除癌症干细胞特性的有前途的方法之一。本文综述了癌症细胞干性的可能靶点,以期实现癌症的完全治疗。