Department of Hematology, Oncology, Technical University, 81675 Munich, Germany.
Cancer Cell. 2013 Jan 14;23(1):77-92. doi: 10.1016/j.ccr.2012.12.003.
Tumor cell survival critically depends on heterotypic communication with benign cells in the microenvironment. Here, we describe a survival signaling pathway activated in stromal cells by contact to B cells from patients with chronic lymphocytic leukemia (CLL). The expression of protein kinase C (PKC)-βII and the subsequent activation of NF-κB in bone marrow stromal cells are prerequisites to support the survival of malignant B cells. PKC-β knockout mice are insusceptible to CLL transplantations, underscoring the in vivo significance of the PKC-βII-NF-κB signaling pathway in the tumor microenvironment. Upregulated stromal PKC-βII in biopsies from patients with CLL, acute lymphoblastic leukemia, and mantle cell lymphoma suggests that this pathway may commonly be activated in a variety of hematological malignancies.
肿瘤细胞的存活严重依赖于微环境中与良性细胞的异质型通讯。在这里,我们描述了一条在基质细胞中被激活的生存信号通路,该通路由慢性淋巴细胞白血病(CLL)患者的 B 细胞接触所激活。骨髓基质细胞中蛋白激酶 C(PKC)-βII 的表达和随后的 NF-κB 的激活是支持恶性 B 细胞存活的前提条件。PKC-β 敲除小鼠对 CLL 移植不易感,这突显了 PKC-βII-NF-κB 信号通路在肿瘤微环境中的体内意义。CLL、急性淋巴细胞白血病和套细胞淋巴瘤患者活检中上调的基质 PKC-βII 表明,该通路可能在多种血液恶性肿瘤中普遍被激活。