Tu Lan Chun, Foltz Greg, Lin Edward, Hood Leroy, Tian Qiang
Institute for Systems Biology, Seattle, WA 98103, USA.
Curr Stem Cell Res Ther. 2009 May;4(2):147-53. doi: 10.2174/157488809788167373.
Cancer stem cells (CSC), also called tumor initiating cells (TIC), are considered to be the origin of replicating malignant tumor cells in a variety of human cancers. Their presence in the tumor may herald malignancy potential, mediate resistance to conventional chemotherapy or radiotherapy, and confer poor survival outcomes. Thus, CSC may serve as critical cellular targets for treatment. The ability to therapeutically target CSC hinges upon identifying their unique cell surface markers and the underlying survival signaling pathways. While accumulating evidence suggests cell-surface antigens (such as CD44, CD133) as CSC markers for several tumor tissues, emerging clinical needs exist for the identification of new markers to completely separate CSC from normal stem cells. Recent studies have demonstrated the critical role of the tumor suppressor PTEN/PI3 kinase pathway in regulating TIC in leukemia, brain, and intestinal tissues. The successful eradication of tumors by therapies targeting CSC will require an in-depth understanding of the molecular mechanisms governing CSC self renewal, differentiation, and escape from conventional therapy. Here we review recent progress from brain tumor and intestinal stem cell research with a focus on the PTEN-Akt-Wnt pathway, and how the components of CSC pathways may serve as biomarkers for diagnosis, prognosis, and therapeutics.
癌症干细胞(CSC),也被称为肿瘤起始细胞(TIC),被认为是多种人类癌症中复制性恶性肿瘤细胞的起源。它们在肿瘤中的存在可能预示着恶性潜能,介导对传统化疗或放疗的抗性,并导致不良的生存结果。因此,癌症干细胞可能是治疗的关键细胞靶点。治疗性靶向癌症干细胞的能力取决于识别其独特的细胞表面标志物和潜在的生存信号通路。虽然越来越多的证据表明细胞表面抗原(如CD44、CD133)是几种肿瘤组织的癌症干细胞标志物,但仍有新的临床需求,需要鉴定新的标志物以将癌症干细胞与正常干细胞完全区分开来。最近的研究表明,肿瘤抑制因子PTEN/PI3激酶通路在调节白血病、脑和肠道组织中的肿瘤起始细胞方面起着关键作用。通过靶向癌症干细胞的疗法成功根除肿瘤将需要深入了解控制癌症干细胞自我更新、分化以及逃避传统治疗的分子机制。在此,我们综述了脑肿瘤和肠道干细胞研究的最新进展,重点关注PTEN-Akt-Wnt通路,以及癌症干细胞通路的组成部分如何作为诊断、预后和治疗的生物标志物。