| pubmed-article:18313758 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18313758 | lifeskim:mentions | umls-concept:C0001811 | lld:lifeskim |
| pubmed-article:18313758 | lifeskim:mentions | umls-concept:C1520113 | lld:lifeskim |
| pubmed-article:18313758 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:18313758 | pubmed:dateCreated | 2008-4-28 | lld:pubmed |
| pubmed-article:18313758 | pubmed:abstractText | No longer considered to be exclusive to cellular developmental pathways, the Wnt family of secreted cysteine-rich glycosylated proteins has emerged as versatile targets for a variety of conditions that involve cardiovascular disease, aging, cancer, diabetes, neurodegeneration, and inflammation. In particular, modulation of Wnt signaling may fill a critical void for the treatment of disorders that impact upon both cellular survival and cellular longevity. Yet, in some scenarios, Wnt signaling can become the catalyst for disease development or promote cell senescence that can compromise clinical utility. This double edge sword in regards to the role of Wnt and its signaling pathways highlights the critical need to further elucidate the cellular mechanisms governed by Wnt in conjunction with the development of robust pharmacological ligands that may open new avenues for disease treatment. Here we discuss the influence of the Wnt pathway during cell survival, metabolism, and aging in order for one to gain a greater insight for the novel role of Wnt signaling as well as exemplify its unique cellular pathways that influence both normal physiology and disease. | lld:pubmed |
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