Donnenberg V S, Luketich J D, Landreneau R J, DeLoia J A, Basse P, Donnenberg A D
Hillman Cancer Research Pavilion, 5117 Centre Avenue, Suite 2.42, Pittsburgh, PA 15213, USA.
Ernst Schering Found Symp Proc. 2006(5):245-63. doi: 10.1007/2789_2007_054.
ABC transporters are highly conserved and represent a major protective mechanism for barrier tissues as well as adult tissue stem cells. Emerging data support the existence of a cancer stem cell that shares features of tissue stem cells, including the ability to self-renew and undergo dysregulated differentiation. Here we show that a rare population of cells coexpressing MDR transporters and stem cell markers is a common feature across therapy-naive epithelial cancers as well as normal epithelial tissue. MDR+ and MDR- candidate tumor stem and progenitor populations were all capable of generating highly anaplastic transplantable human tumors in NOD/SCID. The finding that rare cells bearing stem cell markers and having intrinsic MDR expression and activity are already present within the tumorigenic compartment before treatment with cytotoxic agents is of critical importance to cancer therapy. Just as damaged normal epithelial tissues regenerate after chemotherapy by virtue of highly protected resting tissue stem cells, the existence of malignant counterparts in therapy-naive epithelial cancers suggests a common mechanism by which normal and tumor stem cells protect themselves against toxic injury.
ABC转运蛋白高度保守,是屏障组织以及成体组织干细胞的主要保护机制。新出现的数据支持存在一种具有组织干细胞特征的癌症干细胞,包括自我更新和发生失调分化的能力。在这里,我们表明,共表达多药耐药(MDR)转运蛋白和干细胞标志物的罕见细胞群体是未经治疗的上皮性癌以及正常上皮组织的共同特征。MDR+和MDR-候选肿瘤干细胞和祖细胞群体都能够在NOD/SCID小鼠中产生高度间变的可移植性人类肿瘤。在用细胞毒性药物治疗之前,肿瘤发生区室中就已经存在带有干细胞标志物且具有内在MDR表达和活性的罕见细胞,这一发现对癌症治疗至关重要。正如受损的正常上皮组织在化疗后借助受到高度保护的静止组织干细胞得以再生一样,未经治疗的上皮性癌中存在恶性对应物,这表明正常干细胞和肿瘤干细胞保护自身免受毒性损伤的共同机制。