PloS one, 2013-04, Vol.8 (4), p.e61342
2013
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- Autor(en) / Beteiligte
- Titel
- Targeted apoptotic effects of thymoquinone and tamoxifen on XIAP mediated Akt regulation in breast cancer
- Ist Teil von
- PloS one, 2013-04, Vol.8 (4), p.e61342
- Ort / Verlag
- United States: Public Library of Science
- Erscheinungsjahr
- 2013
- Quelle
- MEDLINE
- Beschreibungen/Notizen
- X-linked inhibitor of apoptosis protein (XIAP) is constitutively expressed endogenous inhibitor of apoptosis, exhibit its antiapoptotic effect by inactivating key caspases such as caspase-3, caspase-7 and caspase-9 and also play pivotal role in rendering cancer chemoresistance. Our studies showed the coadministration of TQ and TAM resulting in a substantial increase in breast cancer cell apoptosis and marked inhibition of cell growth both in vitro and in vivo. Anti-angiogenic and anti-invasive potential of TQ and TAM was assessed through in vitro studies. This novel combinatorial regimen leads to regulation of multiple cell signaling targets including inactivation of Akt and XIAP degradation. At molecular level, TQ and TAM synergistically lowers XIAP expression resulting in binding and activation of caspase-9 in apoptotic cascade, and interfere with cell survival through PI3-K/Akt pathway by inhibiting Akt phosphorylation. Cleaved caspase-9 further processes other intracellular death substrates such as PARP thereby shifting the balance from survival to apoptosis, indicated by rise in the sub-G1 cell population. This combination also downregulates the expression of Akt-regulated downstream effectors such as Bcl-xL, Bcl-2 and induce expression of Bax, AIF, cytochrome C and p-27. Consistent with these results, overexpression studies further confirmed the involvement of XIAP and its regulatory action on Akt phosphorylation along with procaspase-9 and PARP cleavage in TQ-TAM coadministrated induced apoptosis. The ability of TQ and TAM in inhibiting XIAP was confirmed through siRNA-XIAP cotransfection studies. This novel modality may be a promising tool in breast cancer treatment.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 1932-6203eISSN: 1932-6203DOI: 10.1371/journal.pone.0061342Titel-ID: cdi_plos_journals_1343607068
- Format
- –
- Schlagworte
- 1-Phosphatidylinositol 3-kinase, AKT protein, Angiogenesis, Animals, Antineoplastic Agents - pharmacology, Antineoplastic Agents - therapeutic use, Apoptosis, Apoptosis - drug effects, Apoptosis-inducing factor, Bax protein, Bcl-2 protein, bcl-Associated Death Protein - metabolism, Bcl-x protein, Benzoquinones - pharmacology, Biology, Breast cancer, Breast Neoplasms - blood supply, Breast Neoplasms - enzymology, Breast Neoplasms - pathology, Cancer, Cancer therapies, Cancer treatment, Caspase, Caspase-3, Caspase-7, Caspase-9, Cell Cycle - drug effects, Cell growth, Cell Line, Tumor, Cell Movement - drug effects, Cell Proliferation - drug effects, Cell survival, Cell Survival - drug effects, Chemoresistance, Combinatorial analysis, Cytochrome, Cytochrome c, Deactivation, Dose-Response Relationship, Drug, Down-Regulation - drug effects, Drug Synergism, Female, Glycogen Synthase Kinase 3 - metabolism, Glycogen Synthase Kinase 3 beta, Humans, Inactivation, Inhibitors, Invasiveness, Kinases, Medicine, Mice, Neoplasm Invasiveness, Neovascularization, Pathologic - drug therapy, Phosphorylation, Phosphorylation - drug effects, Poly(ADP-ribose) polymerase, Proto-Oncogene Proteins c-akt - metabolism, Rodents, Signal Transduction - drug effects, Signaling, siRNA, Substrates, Survival, Tamoxifen, Tamoxifen - pharmacology, X-Linked Inhibitor of Apoptosis Protein - metabolism, Xenograft Model Antitumor Assays, XIAP protein