Cancer stem cells (CSCs) account for tumor initiation, invasiveness, metastasis, and recurrence in a broad range of human cancers. Although being a key player in cancer development and progression by stimulating proliferation and metastasis and preventing apoptosis, the role of the transcription factor NF-κB in cancer stem cells is still underestimated. In the present review, we will evaluate the role of NF-κB in CSCs of glioblastoma multiforme, ovarian cancer, multiple myeloma, lung cancer, colon cancer, prostate cancer, as well as cancer of the bone. Next to summarizing current knowledge regarding the presence and contribution of CSCs to the respective types of cancer, we will emphasize NF-κB-mediated signaling pathways directly involved in maintaining characteristics of cancer stem cells associated to tumor progression. Here, we will also focus on the status of NF-κB-activity predominantly in CSC populations and the tumor mass. Genetic alterations leading to NF-κB activity in glioblastoma, ependymoma, and multiple myeloma will be discussed.

To compare mechanical stability of angle-stable locking construct with four screws with conventional five screw locking in intramedullary nailed distal tibia fractures under cyclic loading. Ten pairs of fresh-frozen human cadaveric tibiae were intramedullary nailed and assigned to either an angle-stable locking construct consisting of four screws or conventional five-screw locking. After simulating an unstable distal two-fragmental 42-A3.1 fracture, the specimens were mechanically tested under quasistatic and cyclic sinusoidal axial and torsional loading. Bending stiffness of the angle-stable and the conventional fixation was 644.3 N/° and 416.5 N/°, respectively (P = 0.075, power 0.434). Torsional stiffness of the angle-stable locking (1.91 Nm/°) was significantly higher compared with the conventional one (1.13 Nm/°; P = 0.001, power 0.981). Torsional play of the angle-stable fixation (0.08°) was significantly smaller compared with the conventional one (0.46°; P = 0.002, power 0.965). The angle-stable locking revealed significantly less torsional deformation in the fracture gap after one cycle (0.74°) than the conventional one (1.75°; P = 0.005, power 0.915) and also after 1000 cycles (angle-stable: 1.56°; conventional: 2.51°; P = 0.042, power 0.562). Modes of failure were fracture of the distal fragment, loosening of distal locking screws, nail breakage, and their combination, equally distributed between the groups (P = 0.325). Both the angle-stable locking technique using four screws and conventional locking consisting of five screws showed high biomechanical properties. Hence, angle-stable locking reflects a potential to maintain fixation stability while reducing the number of locking screws compared with conventional locking in intramedullary nailed unstable distal tibia fractures.