<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(1)</volume><submitter>Zhang Y</submitter><pubmed_abstract>SCLIP, a microtubule-destabilizing phosphoprotein, is known to be involved in the development of the central nervous system (CNS). It has been well established that there are notable parallels between normal development and tumorigenesis, especially in glioma. However, no studies have examined the significance of SCLIP in gliomagenesis. To address this, we investigated the expression of SCLIP and its roles in the development of gliomas. Notably, we found that SCLIP was highly expressed in various grades of glioma samples, as compared with normal brain tissues. Overexpression of SCLIP dramatically stimulated tumor cell migration and invasion as well as proliferation and downregulation of SCLIP showed opposite effects, establishing an important oncogenic role for this gene. Furthermore, we r</pubmed_abstract><journal>Cancer biology &amp; therapy</journal><pagination>97-105</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4623355</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Overexpression of SCLIP promotes growth and motility in glioblastoma cells.</pubmed_title><pmcid>PMC4623355</pmcid><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Hao A</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Ni S</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Huang B</pubmed_authors><pubmed_authors>Wang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Overexpression of SCLIP promotes growth and motility in glioblastoma cells.</name><description>SCLIP, a microtubule-destabilizing phosphoprotein, is known to be involved in the development of the central nervous system (CNS). It has been well established that there are notable parallels between normal development and tumorigenesis, especially in glioma. However, no studies have examined the significance of SCLIP in gliomagenesis. To address this, we investigated the expression of SCLIP and its roles in the development of gliomas. Notably, we found that SCLIP was highly expressed in various grades of glioma samples, as compared with normal brain tissues. Overexpression of SCLIP dramatically stimulated tumor cell migration and invasion as well as proliferation and downregulation of SCLIP showed opposite effects, establishing an important oncogenic role for this gene. Furthermore, we r</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2025-04-21T20:29:51.198Z</modification><creation>2019-03-27T02:00:54Z</creation></dates><accession>S-EPMC4623355</accession><cross_references><pubmed>25511414</pubmed><doi>10.4161/15384047.2014.987037</doi></cross_references></HashMap>