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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=TEAD2</id>
	<title>TEAD2 - История изменений</title>
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		<id>https://transhumanist.ru/index.php?title=TEAD2&amp;diff=5443&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «Transcriptional enhancer factor TEF-4 (TEA domain family member 2) (TEAD-2) [TEF4]  ==Publications==  {{medline-entry |title=Novel transcriptional targets of the...»</title>
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		<updated>2021-05-12T13:44:13Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Transcriptional enhancer factor TEF-4 (TEA domain family member 2) (TEAD-2) [TEF4]  ==Publications==  {{medline-entry |title=Novel transcriptional targets of the...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Transcriptional enhancer factor TEF-4 (TEA domain family member 2) (TEAD-2) [TEF4]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Novel transcriptional targets of the [[SRY]]-HMG box transcription factor [[SOX4]] link its expression to the development of small cell lung cancer.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/22084397&lt;br /&gt;
|abstract=The HMG box transcription factor [[SOX4]] involved in neuronal development is amplified and overexpressed in a subset of lung cancers, suggesting that it may be a driver oncogene. In this study, we sought to develop this hypothesis including by defining targets of [[SOX4]] that may mediate its involvement in lung cancer. Ablating [[SOX4]] expression in [[SOX4]]-amplified lung cancer cells revealed a gene expression signature that included genes involved in neuronal development such as PCDHB, [[MYB]], [[RBP1]], and [[TEAD2]]. Direct recruitment of [[SOX4]] to gene promoters was associated with their upregulation upon ectopic overexpression of [[SOX4]]. We confirmed upregulation of the [[SOX4]] expression signature in a panel of primary lung tumors, validating their specific response by a comparison using embryonic fibroblasts from Sox4-deficient mice. Interestingly, we found that small cell lung cancer (SCLC), a subtype of lung cancer with neuroendocrine characteristics, was generally characterized by high levels of [[SOX2]], [[SOX4]], and [[SOX11]] along with the [[SOX4]]-specific gene expression signature identified. Taken together, our findings identify a functional role for SOX genes in SCLC, particularly for [[SOX4]] and several novel targets defined in this study.&lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Blotting, Western&lt;br /&gt;
* Carcinoma, Small Cell&lt;br /&gt;
* Cell Line, Tumor&lt;br /&gt;
* Chromatin Immunoprecipitation&lt;br /&gt;
* Gene Expression&lt;br /&gt;
* Humans&lt;br /&gt;
* Lung Neoplasms&lt;br /&gt;
* Mice&lt;br /&gt;
* Promoter Regions, Genetic&lt;br /&gt;
* Real-Time Polymerase Chain Reaction&lt;br /&gt;
* SOXC Transcription Factors&lt;br /&gt;
* Transcription, Genetic&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1158/0008-5472.CAN-11-3506&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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