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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=ARID5A</id>
	<title>ARID5A - История изменений</title>
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	<updated>2026-08-18T12:18:57Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=ARID5A&amp;diff=4524&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «AT-rich interactive domain-containing protein 5A (ARID domain-containing protein 5A) (Modulator recognition factor 1) (MRF-1) [MRF1]  ==Publications==  {{medline-...»</title>
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		<updated>2021-04-29T19:22:11Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «AT-rich interactive domain-containing protein 5A (ARID domain-containing protein 5A) (Modulator recognition factor 1) (MRF-1) [MRF1]  ==Publications==  {{medline-...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;AT-rich interactive domain-containing protein 5A (ARID domain-containing protein 5A) (Modulator recognition factor 1) (MRF-1) [MRF1]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Differentially regulated gene expression in quiescence versus senescence and identification of [[ARID5A]] as a quiescence associated marker.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29044508&lt;br /&gt;
|abstract=In multicellular organisms majority of the cells remain in a non-dividing states of either quiescence (reversible) or senescence (irreversible). In the present study, gene expression signatures unique to quiescence and senescence were identified using microarray in osteosarcoma cell line, U2OS. It was noted that certain genes and pathways like NOD pathway was shared by both the growth arrest conditions. A major highlight of the present study was increased expression of number of chemokines and cytokines in both quiescence and senescence. While senescence-associated secretory phenotype (SASP) is well known, the quiescence-associated secretory phenotype (QASP) is relatively unknown and appeared novel in this study. [[ARID5A]], a subunit of SWI/SNF complex was identified as a quiescence associated gene. The endogenous expression of [[ARID5A]] increased during serum starved condition of quiescence. Overexpression of [[ARID5A]] resulted in more number of cells in G0/G1 phase of cell cycle. Further [[ARID5A]] overexpressing cells when subjected to serum starvation showed a pronounced secretory phenotype. Overall, the present work has identified gene expression signatures which can distinguish quiescence from senescence.&lt;br /&gt;
|mesh-terms=* Biomarkers&lt;br /&gt;
* Cell Cycle&lt;br /&gt;
* Cell Cycle Checkpoints&lt;br /&gt;
* Cell Division&lt;br /&gt;
* Cell Line, Tumor&lt;br /&gt;
* Cellular Senescence&lt;br /&gt;
* Cytokines&lt;br /&gt;
* DNA-Binding Proteins&lt;br /&gt;
* Humans&lt;br /&gt;
* Nuclear Proteins&lt;br /&gt;
* Phenotype&lt;br /&gt;
* Signal Transduction&lt;br /&gt;
|keywords=* ARID5A&lt;br /&gt;
* inflammasome&lt;br /&gt;
* quiescence&lt;br /&gt;
* secretory phenotype&lt;br /&gt;
* senescence&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1002/jcp.26227&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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