Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198-5870, USA.
J Ovarian Res. 2008 Oct 12;1(1):4. doi: 10.1186/1757-2215-1-4.
Emerging evidence suggests that the capacity of a tumor to grow and propagate is dependent on a small subset of cells within a tumor, termed cancer stem cells. In fact, cancer cells, like stem cells, can proliferate indefinitely through a dysregulated cellular self-renewal capacity. Cancer stem cells may originate due to the distribution into self-renewal and differentiation pathways occurring in multi-potential stem cells, tissue-specific stem cells, progenitor cells and cancer cells. Recent studies have shown that ovarian cancer also contains stem cells or tumor-initiating cells. Moreover, ovarian serous adenocarcinomas were disaggregated and subjected to growth conditions to select for self-renewing, non-adherent spheroids previously shown to be derived from tissue stem cells. A recent study showed that epithelial ovarian cancer was derived from a sub population of CD44+, CD117+ and CD133+ cells. The existence of cancer stem cells would explain why only a small minority of cancer cells is capable of extensive proliferation of the tumor. In this review, we have discussed the studies on ovarian cancer stem cells along with the molecular pathways that could be involved in these cancer stem cells.
新出现的证据表明,肿瘤生长和增殖的能力取决于肿瘤内一小部分称为癌症干细胞的细胞。事实上,癌细胞和干细胞一样,可以通过失调的细胞自我更新能力无限增殖。癌症干细胞可能源于多潜能干细胞、组织特异性干细胞、祖细胞和癌细胞中发生的自我更新和分化途径的分布。最近的研究表明,卵巢癌也含有干细胞或肿瘤起始细胞。此外,将卵巢浆液性腺癌进行离散,并在生长条件下进行选择,以获得先前显示源自组织干细胞的自我更新、非黏附的球体。最近的一项研究表明,上皮性卵巢癌来源于 CD44+、CD117+和 CD133+细胞的亚群。癌症干细胞的存在可以解释为什么只有少数癌细胞能够广泛增殖肿瘤。在这篇综述中,我们讨论了卵巢癌干细胞的研究以及可能涉及这些癌症干细胞的分子途径。