Department of Biochemistry and Molecular Biology and Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE 68198-5870, USA.
Anticancer Agents Med Chem. 2010 Feb;10(2):137-51. doi: 10.2174/187152010790909353.
A growing body of experimental evidence has revealed that the highly tumorigenic cancer stem/progenitor cells endowed with stem cell-like properties might be responsible for initiation and progression of numerous aggressive epithelial cancers into locally invasive, metastatic and incurable disease states. The malignant transformation of tissue-resident adult stem/progenitor cells or their progenies into tumorigenic and migrating cancer stem/progenitor cells and their resistance to current cancer therapies have been associated with their high expression levels of specific oncogenic products and drug resistance-associated molecules. In this regard, we describe the tumorigenic cascades that are frequently activated in cancer stem/progenitor cells versus their differentiated progenies during the early and late stages of the epithelial cancer progression. The emphasis is on the growth factor signaling pathways involved in the malignant behavior of prostate and pancreatic cancer stem/progenitor cells and their progenies. Of clinical interest, the potential molecular therapeutic targets to eradicate the tumor- and metastasis-initiating cells and their progenies and develop new effective combination therapies against locally advanced and metastatic epithelial cancers are also described.
越来越多的实验证据表明,具有干细胞样特性的高致瘤性肿瘤干细胞/祖细胞可能是导致许多侵袭性上皮癌发展为局部浸润、转移和不可治愈疾病状态的原因。组织驻留的成体干细胞/祖细胞或其后代向致瘤性和迁移性肿瘤干细胞/祖细胞的恶性转化及其对现有癌症治疗的耐药性与它们高水平表达特定致癌产物和耐药相关分子有关。在这方面,我们描述了在上皮癌进展的早期和晚期,肿瘤干细胞/祖细胞与其分化后代中经常被激活的肿瘤发生级联反应。重点是涉及前列腺癌和胰腺癌干细胞/祖细胞及其后代恶性行为的生长因子信号通路。值得关注的是,消灭肿瘤起始细胞和转移起始细胞及其后代的潜在分子治疗靶点,并开发针对局部晚期和转移性上皮癌的新有效联合治疗方法也在研究中。