Senescence: a new weapon for cancer therapy
- PMID: 22245068
- DOI: 10.1016/j.tcb.2011.11.006
Senescence: a new weapon for cancer therapy
Abstract
Senescence is a stable cell cycle arrest that can be activated by oncogenic signaling and manifests with changes in cellular organization and gene expression, such as the induction of a complex secretome. Importantly, senescence limits tumor progression and determines the outcome of conventional anticancer therapies. In recent years, therapeutic approaches such as p53 reactivation, inhibition of c-MYC in addicted tumors or treatment with cyclin-dependent kinase (CDK) inhibitors have proven effective by invoking a senescence response. The possibility of using prosenescence therapies for cancer treatment has provoked considerable interest. We propose that the senescence secretome can be a source of novel targets for prosenescence therapies, as it has tumor suppressive actions. Overall, tailored prosenescence therapies have the potential to be used for treating cancer and other pathologies.
Copyright © 2011 Elsevier Ltd. All rights reserved.
Similar articles
-
Molecular pathways: harnessing E2F1 regulation for prosenescence therapy in p53-defective cancer cells.Clin Cancer Res. 2014 Jul 15;20(14):3644-50. doi: 10.1158/1078-0432.CCR-13-1942. Epub 2014 May 1. Clin Cancer Res. 2014. PMID: 24788101 Review.
-
Senescence of Tumor Cells in Anticancer Therapy-Beneficial and Detrimental Effects.Int J Mol Sci. 2022 Sep 21;23(19):11082. doi: 10.3390/ijms231911082. Int J Mol Sci. 2022. PMID: 36232388 Free PMC article. Review.
-
Two-Step Senescence-Focused Cancer Therapies.Trends Cell Biol. 2018 Sep;28(9):723-737. doi: 10.1016/j.tcb.2018.04.006. Epub 2018 May 17. Trends Cell Biol. 2018. PMID: 29776716 Free PMC article. Review.
-
The p53 transcriptional response across tumor types reveals core and senescence-specific signatures modulated by long noncoding RNAs.Proc Natl Acad Sci U S A. 2021 Aug 3;118(31):e2025539118. doi: 10.1073/pnas.2025539118. Proc Natl Acad Sci U S A. 2021. PMID: 34326251 Free PMC article.
-
Novel ARF/p53-independent senescence pathways in cancer repression.J Mol Med (Berl). 2011 Sep;89(9):857-67. doi: 10.1007/s00109-011-0766-y. Epub 2011 May 19. J Mol Med (Berl). 2011. PMID: 21594579 Free PMC article. Review.
Cited by
-
Identification and characterization of aging/senescence-induced genes in osteosarcoma and predicting clinical prognosis.Front Immunol. 2022 Oct 5;13:997765. doi: 10.3389/fimmu.2022.997765. eCollection 2022. Front Immunol. 2022. PMID: 36275664 Free PMC article.
-
Repopulation of ovarian cancer cells after chemotherapy.Cancer Growth Metastasis. 2013 Feb 18;6:15-21. doi: 10.4137/CGM.S11333. Cancer Growth Metastasis. 2013. PMID: 23544004 Free PMC article.
-
Radiation driven epithelial-mesenchymal transition is mediated by Notch signaling in breast cancer.Oncotarget. 2016 Aug 16;7(33):53430-53442. doi: 10.18632/oncotarget.10802. Oncotarget. 2016. PMID: 27462787 Free PMC article.
-
Induction of Therapeutic Senescence in Vemurafenib-Resistant Melanoma by Extended Inhibition of CDK4/6.Cancer Res. 2016 May 15;76(10):2990-3002. doi: 10.1158/0008-5472.CAN-15-2931. Epub 2016 Mar 17. Cancer Res. 2016. PMID: 26988987 Free PMC article.
-
Targeting of cancer cell death mechanisms by resveratrol: a review.Apoptosis. 2021 Dec;26(11-12):561-573. doi: 10.1007/s10495-021-01689-7. Epub 2021 Sep 25. Apoptosis. 2021. PMID: 34561763 Review.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous