| pubmed-article:21345215 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21345215 | lifeskim:mentions | umls-concept:C0006826 | lld:lifeskim |
| pubmed-article:21345215 | lifeskim:mentions | umls-concept:C0031831 | lld:lifeskim |
| pubmed-article:21345215 | lifeskim:mentions | umls-concept:C1155342 | lld:lifeskim |
| pubmed-article:21345215 | pubmed:dateCreated | 2011-3-18 | lld:pubmed |
| pubmed-article:21345215 | pubmed:abstractText | The unfolded protein response (UPR) is a cascade of intracellular stress signaling events in response to an accumulation of unfolded or misfolded proteins in the lumen of the endoplasmic reticulum (ER). Cancer cells are often exposed to hypoxia, nutrient starvation, oxidative stress and other metabolic dysregulation that cause ER stress and activation of the UPR. Depending on the duration and degree of ER stress, the UPR can provide either survival signals by activating adaptive and antiapoptotic pathways, or death signals by inducing cell death programs. Sustained induction or repression of UPR pharmacologically may thus have beneficial and therapeutic effects against cancer. In this review, we discuss the basic mechanisms of UPR and highlight the importance of UPR in cancer biology. We also update the UPR-targeted cancer therapeutics currently in clinical trials. | lld:pubmed |
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