Wnt signaling pathway: Implications for therapy in lung cancer and bone metastasis |
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Authors: | Yongming Xi Yan Chen |
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Affiliation: | 1. Department of Orthopaedics, Affiliated Hospital of Qingdao University, China;2. Division in Signaling Biology, Ontario Cancer Institute, University Health Network, Toronto, Canada |
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Abstract: | Lung cancer remains a major worldwide health problem and patients have high rate of metastasis including bone. Although pathologic characteristics of this disease are clear and well established, much remains to be understood about this tumor, particularly at the molecular signaling level. Secreted signaling molecules of the Wnt family have been widely investigated and found to play a prominent role to induce human malignant diseases, such as breast and prostate cancer. A variety of studies have also demonstrated that the Wnt signaling pathway is closely associated with bone malignancies including osteosarcoma, multiple myeloma, and breast or prostate cancer induced bone metastasis. The aim of this review is to provide a summary regarding the role of the Wnt signaling pathway in lung cancer and bone metastasis, highlighting the aberrant activation of Wnt in this malignancy. We also discuss the potential therapeutic applications for the treatment of lung cancer and cancer induced bone metastasis targeting the Wnt pathway. |
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Keywords: | APC, adenomatosis polyposis coli CaMKII, calcium/calmodulin-dependent protein kinase II CSC, cancer stem cell CCND1, Cyclin D1 Cox-2, Cyclooxygenase 2 Dkk, dickkopf Dvl, dishevelled Fz, frizzled GSK-3β, glycogen synthase kinase 3β JNK, c-Jun N-terminal Kinase LEF, lymphoid enhancer factor LRP, low-density lipoprotein receptor related protein NF κB, nuclear factor kappa-light-chain-enhancer of activated B cells PCP, planar cell polarity ROR, receptor tyrosine kinase-like orphan receptor ROS, reactive oxygen species RTK, receptor tyrosine kinase RNAi, RNA interference sFRP, secreted frizzled-related protein TCF, T cell factor WIF-1, Wnt inhibitory factor 1 |
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