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Dynamics of p53 and Wnt cross talk
[Display omitted] •The cross-talk between Wnt and p53 signaling pathways allows to regulate each other.•Nutlin can able to switch on the somitogenesis at low Axin2 level.•Excess Axin2 level in Wnt pathway could trigger the cell to apoptotic phase.•Control of one reaction could probably save the cell...
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Published in: | Computational biology and chemistry 2015-12, Vol.59, p.55-66 |
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container_title | Computational biology and chemistry |
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creator | Zubbair Malik, Md Ali, Shahnawaz Jahoor Alam, Md Ishrat, Romana Brojen Singh, R.K. |
description | [Display omitted]
•The cross-talk between Wnt and p53 signaling pathways allows to regulate each other.•Nutlin can able to switch on the somitogenesis at low Axin2 level.•Excess Axin2 level in Wnt pathway could trigger the cell to apoptotic phase.•Control of one reaction could probably save the cell going from apoptotic phase.
We present the mechanism of interaction of Wnt network module, which is responsible for periodic somitogenesis, with p53 regulatory network, which is one of the main regulators of various cellular functions, and switching of various oscillating states by investigating p53–Wnt model. The variation in Nutlin concentration in p53 regulating network drives the Wnt network module to different states, stabilized, damped and sustain oscillation states, and even to cycle arrest. Similarly, the change in Axin2 concentration in Wnt could able to modulate the p53 dynamics at these states. We then solve the set of coupled ordinary differential equations of the model using quasi steady state approximation. We, further, demonstrate the change of p53 and GSK3 interaction rate, due to hypothetical catalytic reaction or external stimuli, can able to regulate the dynamics of the two network modules, and even can control their dynamics to protect the system from cycle arrest (apoptosis). |
doi_str_mv | 10.1016/j.compbiolchem.2015.07.014 |
format | article |
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•The cross-talk between Wnt and p53 signaling pathways allows to regulate each other.•Nutlin can able to switch on the somitogenesis at low Axin2 level.•Excess Axin2 level in Wnt pathway could trigger the cell to apoptotic phase.•Control of one reaction could probably save the cell going from apoptotic phase.
We present the mechanism of interaction of Wnt network module, which is responsible for periodic somitogenesis, with p53 regulatory network, which is one of the main regulators of various cellular functions, and switching of various oscillating states by investigating p53–Wnt model. The variation in Nutlin concentration in p53 regulating network drives the Wnt network module to different states, stabilized, damped and sustain oscillation states, and even to cycle arrest. Similarly, the change in Axin2 concentration in Wnt could able to modulate the p53 dynamics at these states. We then solve the set of coupled ordinary differential equations of the model using quasi steady state approximation. We, further, demonstrate the change of p53 and GSK3 interaction rate, due to hypothetical catalytic reaction or external stimuli, can able to regulate the dynamics of the two network modules, and even can control their dynamics to protect the system from cycle arrest (apoptosis).</description><identifier>ISSN: 1476-9271</identifier><identifier>EISSN: 1476-928X</identifier><identifier>DOI: 10.1016/j.compbiolchem.2015.07.014</identifier><identifier>PMID: 26375870</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Apoptosis ; Axin Protein - metabolism ; Fixed point oscillations ; Gene Regulatory Networks - genetics ; Glycogen Synthase Kinase 3 - metabolism ; Humans ; Imidazoles - metabolism ; Models, Biological ; Nutlin ; p53 activation ; Piperazines - metabolism ; Sustain oscillations ; Tumor Suppressor Protein p53 - genetics ; Tumor Suppressor Protein p53 - metabolism ; Wnt ; Wnt Signaling Pathway - genetics</subject><ispartof>Computational biology and chemistry, 2015-12, Vol.59, p.55-66</ispartof><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c380t-7c46827d99cc6e6580b4a394aa6810edc709707456b46f4e9f13064f17c818d83</citedby><cites>FETCH-LOGICAL-c380t-7c46827d99cc6e6580b4a394aa6810edc709707456b46f4e9f13064f17c818d83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26375870$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zubbair Malik, Md</creatorcontrib><creatorcontrib>Ali, Shahnawaz</creatorcontrib><creatorcontrib>Jahoor Alam, Md</creatorcontrib><creatorcontrib>Ishrat, Romana</creatorcontrib><creatorcontrib>Brojen Singh, R.K.</creatorcontrib><title>Dynamics of p53 and Wnt cross talk</title><title>Computational biology and chemistry</title><addtitle>Comput Biol Chem</addtitle><description>[Display omitted]
•The cross-talk between Wnt and p53 signaling pathways allows to regulate each other.•Nutlin can able to switch on the somitogenesis at low Axin2 level.•Excess Axin2 level in Wnt pathway could trigger the cell to apoptotic phase.•Control of one reaction could probably save the cell going from apoptotic phase.
We present the mechanism of interaction of Wnt network module, which is responsible for periodic somitogenesis, with p53 regulatory network, which is one of the main regulators of various cellular functions, and switching of various oscillating states by investigating p53–Wnt model. The variation in Nutlin concentration in p53 regulating network drives the Wnt network module to different states, stabilized, damped and sustain oscillation states, and even to cycle arrest. Similarly, the change in Axin2 concentration in Wnt could able to modulate the p53 dynamics at these states. We then solve the set of coupled ordinary differential equations of the model using quasi steady state approximation. We, further, demonstrate the change of p53 and GSK3 interaction rate, due to hypothetical catalytic reaction or external stimuli, can able to regulate the dynamics of the two network modules, and even can control their dynamics to protect the system from cycle arrest (apoptosis).</description><subject>Apoptosis</subject><subject>Axin Protein - metabolism</subject><subject>Fixed point oscillations</subject><subject>Gene Regulatory Networks - genetics</subject><subject>Glycogen Synthase Kinase 3 - metabolism</subject><subject>Humans</subject><subject>Imidazoles - metabolism</subject><subject>Models, Biological</subject><subject>Nutlin</subject><subject>p53 activation</subject><subject>Piperazines - metabolism</subject><subject>Sustain oscillations</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><subject>Wnt</subject><subject>Wnt Signaling Pathway - genetics</subject><issn>1476-9271</issn><issn>1476-928X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkMlOwzAQhi0EoqXwCijqiUvCOHa8cEMtm1SJCwhuluNMhEuWEqdIfXtSChVHTjOH75_lI2RKIaFAxeUycW29yn1buTeskxRoloBMgPIDMqZcilin6vVw30s6IichLAFSBpAdk1EqmMyUhDGZzjeNrb0LUVtGq4xFtimil6aPXNeGEPW2ej8lR6WtAp791Al5vr15mt3Hi8e7h9n1InZMQR9Lx4VKZaG1cwJFpiDnlmlurVAUsHAStATJM5FzUXLUJWUgeEmlU1QVik3IxW7uqms_1hh6U_vgsKpsg-06GCoz4CzVWg_o1Q79vrLD0qw6X9tuYyiYrSOzNH8dma0jA9IMjobw-c-edV5jsY_-ShmA-Q7A4dtPj50JzmPjsPAdut4Urf_Pni-rJnvH</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>Zubbair Malik, Md</creator><creator>Ali, Shahnawaz</creator><creator>Jahoor Alam, Md</creator><creator>Ishrat, Romana</creator><creator>Brojen Singh, R.K.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201512</creationdate><title>Dynamics of p53 and Wnt cross talk</title><author>Zubbair Malik, Md ; Ali, Shahnawaz ; Jahoor Alam, Md ; Ishrat, Romana ; Brojen Singh, R.K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-7c46827d99cc6e6580b4a394aa6810edc709707456b46f4e9f13064f17c818d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Apoptosis</topic><topic>Axin Protein - metabolism</topic><topic>Fixed point oscillations</topic><topic>Gene Regulatory Networks - genetics</topic><topic>Glycogen Synthase Kinase 3 - metabolism</topic><topic>Humans</topic><topic>Imidazoles - metabolism</topic><topic>Models, Biological</topic><topic>Nutlin</topic><topic>p53 activation</topic><topic>Piperazines - metabolism</topic><topic>Sustain oscillations</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><topic>Wnt</topic><topic>Wnt Signaling Pathway - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zubbair Malik, Md</creatorcontrib><creatorcontrib>Ali, Shahnawaz</creatorcontrib><creatorcontrib>Jahoor Alam, Md</creatorcontrib><creatorcontrib>Ishrat, Romana</creatorcontrib><creatorcontrib>Brojen Singh, R.K.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Computational biology and chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zubbair Malik, Md</au><au>Ali, Shahnawaz</au><au>Jahoor Alam, Md</au><au>Ishrat, Romana</au><au>Brojen Singh, R.K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamics of p53 and Wnt cross talk</atitle><jtitle>Computational biology and chemistry</jtitle><addtitle>Comput Biol Chem</addtitle><date>2015-12</date><risdate>2015</risdate><volume>59</volume><spage>55</spage><epage>66</epage><pages>55-66</pages><issn>1476-9271</issn><eissn>1476-928X</eissn><abstract>[Display omitted]
•The cross-talk between Wnt and p53 signaling pathways allows to regulate each other.•Nutlin can able to switch on the somitogenesis at low Axin2 level.•Excess Axin2 level in Wnt pathway could trigger the cell to apoptotic phase.•Control of one reaction could probably save the cell going from apoptotic phase.
We present the mechanism of interaction of Wnt network module, which is responsible for periodic somitogenesis, with p53 regulatory network, which is one of the main regulators of various cellular functions, and switching of various oscillating states by investigating p53–Wnt model. The variation in Nutlin concentration in p53 regulating network drives the Wnt network module to different states, stabilized, damped and sustain oscillation states, and even to cycle arrest. Similarly, the change in Axin2 concentration in Wnt could able to modulate the p53 dynamics at these states. We then solve the set of coupled ordinary differential equations of the model using quasi steady state approximation. We, further, demonstrate the change of p53 and GSK3 interaction rate, due to hypothetical catalytic reaction or external stimuli, can able to regulate the dynamics of the two network modules, and even can control their dynamics to protect the system from cycle arrest (apoptosis).</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26375870</pmid><doi>10.1016/j.compbiolchem.2015.07.014</doi><tpages>12</tpages></addata></record> |
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subjects | Apoptosis Axin Protein - metabolism Fixed point oscillations Gene Regulatory Networks - genetics Glycogen Synthase Kinase 3 - metabolism Humans Imidazoles - metabolism Models, Biological Nutlin p53 activation Piperazines - metabolism Sustain oscillations Tumor Suppressor Protein p53 - genetics Tumor Suppressor Protein p53 - metabolism Wnt Wnt Signaling Pathway - genetics |
title | Dynamics of p53 and Wnt cross talk |
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