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	<title>SHOX2 - История изменений</title>
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	<updated>2026-05-15T07:57:15Z</updated>
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		<title>OdysseusBot: Новая страница: «Short stature homeobox protein 2 (Homeobox protein Og12X) (Paired-related homeobox protein SHOT) [OG12X] [SHOT]  ==Publications==  {{medline-entry |title=Role of...»</title>
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		<updated>2021-04-29T19:19:57Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «Short stature homeobox protein 2 (Homeobox protein Og12X) (Paired-related homeobox protein SHOT) [OG12X] [SHOT]  ==Publications==  {{medline-entry |title=Role of...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Short stature homeobox protein 2 (Homeobox protein Og12X) (Paired-related homeobox protein SHOT) [OG12X] [SHOT]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Role of [[SHOX2]] in the development of intervertebral disc degeneration.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26697824&lt;br /&gt;
|abstract=Intervertebral disc ([[IVD]]) degeneration is the most common cause of low back pain, which affect 80% of the population during their lives, with heavy economic burden. Many factors have been demonstrated to participate in [[IVD]] degeneration. In this study, we investigated the role of short stature homeobox 2 ([[SHOX2]]) in the development of [[IVD]] degeneration. First, we detected the expression of [[SHOX2]] in different stages of human [[IVD]] degeneration; then explored the role of [[SHOX2]] on nucleus pulposus (NP) cells proliferation and apoptosis, finally we evaluated the effect of [[SHOX2]] on the production of extracellular matrix in NP cells. Results showed that the expression of [[SHOX2]] is mainly in NP compared with AF tissues, its expression decreased with the severity of human [[IVD]] degeneration. [[TNF]]-α treatment led to dose- and time-dependent decrease in [[SHOX2]] mRNA, protein expression and promoter activity in NP cells. The silencing of [[SHOX2]] inhibited NP cells proliferation and induced NP cells apoptosis. Finally, [[SHOX2]] silencing led to decreased aggrecan and collagen II expression, along with increased ECM degrading enzymes [[MMP3]] and ADAMTS-5 in NP cells. In summary, our results indicated that [[SHOX2]] plays an important role in the process of [[IVD]] degeneration, and might be a protective factor for [[IVD]] degeneration. Further studies are required to confirm its exact role, and clarify the mechanism. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 35:1047-1057, 2017.&lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Apoptosis&lt;br /&gt;
* Cell Proliferation&lt;br /&gt;
* Extracellular Matrix&lt;br /&gt;
* Homeodomain Proteins&lt;br /&gt;
* Intervertebral Disc Degeneration&lt;br /&gt;
* Nucleus Pulposus&lt;br /&gt;
* Primary Cell Culture&lt;br /&gt;
* Rats, Sprague-Dawley&lt;br /&gt;
* Tumor Necrosis Factor-alpha&lt;br /&gt;
|keywords=* SHOX2 gene&lt;br /&gt;
* TNF-α&lt;br /&gt;
* intervertebral disc degeneration&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1002/jor.23140&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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