Saeg Fouad, Anbalagan Muralidharan
Department of Structural and Cellular Biology, Tulane University School of Medicine, New Orleans, LA, USA.
DeBakey Scholars Program, Tulane University School of Medicine, New Orleans, LA, USA.
Stem Cell Investig. 2018 Oct 31;5:39. doi: 10.21037/sci.2018.10.05. eCollection 2018.
Breast cancer is a heterogeneous disease that accounts for 30% of all cancers diagnosed in women and over half a million deaths per year. Cancer stem cells (CSCs) make up a small subpopulation of cells within a tumor, are capable of self-renewal and, are responsible for tumor initiation, formation, and recurrence. Breast CSCs (BCSCs) have been the subject of concentrated research as potential targets for breast cancer therapies. Cell surface markers CD44+/CD24- have been established as minimum biomarkers for BCSCs and the upregulation of CD44 expression has been linked to tumor formation in numerous cancers. Additionally, the deregulation of Notch, Wnt/Frizzled/β-catenin, Hippo, and Hedgehog signaling pathways is believed to be responsible for the formation of CSCs and lead to tumor formation. Tumor heterogeneity is a key feature of therapy resistance and a major challenge. CSCs are predominantly senescent and inherently immune to chemotherapy drugs which rely on an overactive cell cycle. Current therapeutic strategies include targeting CSC signaling pathways that play critical roles in self-renewal and defense. Anti-CD44 antibodies have been shown to induce terminal differentiation in CSCs resulting in a significant decrease in tumor metastasis. Additionally, targeting the tumor microenvironment has been shown to increase the effectiveness of chemotherapy drugs. In this review, we attempt to provide an overview of breast cancer, the stem of its cause, and novel therapies currently being explored.
乳腺癌是一种异质性疾病,占女性确诊癌症的30%,每年导致超过50万人死亡。癌症干细胞(CSCs)是肿瘤内一小部分细胞,能够自我更新,并负责肿瘤的起始、形成和复发。乳腺癌症干细胞(BCSCs)作为乳腺癌治疗的潜在靶点,一直是集中研究的对象。细胞表面标志物CD44+/CD24-已被确立为BCSCs的最小生物标志物,CD44表达的上调与多种癌症的肿瘤形成有关。此外,Notch、Wnt/Frizzled/β-连环蛋白、Hippo和Hedgehog信号通路的失调被认为是CSCs形成的原因,并导致肿瘤形成。肿瘤异质性是治疗耐药的关键特征和主要挑战。CSCs主要处于衰老状态,对依赖过度活跃细胞周期的化疗药物具有内在抗性。目前的治疗策略包括靶向在自我更新和防御中起关键作用的CSC信号通路。抗CD44抗体已被证明可诱导CSCs终末分化,从而显著降低肿瘤转移。此外,靶向肿瘤微环境已被证明可提高化疗药物的有效性。在这篇综述中,我们试图概述乳腺癌、其病因根源以及目前正在探索的新疗法。