<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-30T05:33:43Z</responseDate><request verb="GetRecord" identifier="oai:munzur-rdlopen.rawdatalibrary.net:munzur/3687" metadataPrefix="oai_dc">https://munzur-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:munzur-rdlopen.rawdatalibrary.net:munzur/3687</identifier><datestamp>2026-10-28T15:39:33Z</datestamp><setSpec>openaire</setSpec><setSpec>com_munzur_1</setSpec><setSpec>col_munzur_2</setSpec><setSpec>com_munzur_8</setSpec><setSpec>col_munzur_159</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Regulation of signaling pathways by β-elemene in cancer progression and metastasis</dc:title><dc:creator>Qureshi, Muhammad Z.</dc:creator><dc:creator>Attar, Rukset</dc:creator><dc:creator>Romero, Mirna A.</dc:creator><dc:creator>Sabitaliyevich, Uteuliyev Y.</dc:creator><dc:creator>Nurmurzayevich, Sadykov B.</dc:creator><dc:creator>Ozturk, Ozlem</dc:creator><dc:creator>Wakim, Lara H.</dc:creator><dc:creator>Lin, Xiukun</dc:creator><dc:creator>Ozbey, Ulku</dc:creator><dc:creator>Yelekenova, Armida Bakhytbekovna</dc:creator><dc:creator>Farooqi, Ammad A.</dc:creator><dc:subject>apoptosis</dc:subject><dc:subject>cancer</dc:subject><dc:subject>elemene</dc:subject><dc:subject>signaling</dc:subject><dc:description>Entry of β-elemene into various phases of clinical trials advocates its significance as a premium candidate likely to gain access to mainstream medicine. Based on the insights gleaned from decades of research, it seems increasingly transparent that β-elemene has shown significant ability to modulate multiple cell signaling pathways in different cancers. We partition this multicomponent review into how β-elemene strategically modulates various signal transduction cascades. We have individually summarized regulation of tumor necrosis factor related apoptosis-inducing ligand, signal transducers and activators of transcription, transforming growth factor/SMAD, NOTCH, and mammalian target of rapamycin pathways by β-elemene. Last, we will discuss the results of clinical trials of β-elemene and how effectively we can use these findings to stratify patients who can benefit most from β-elemene.</dc:description><dc:publisher>Wiley-Liss Inc.</dc:publisher><dc:date>2019</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/munzur/3687</dc:identifier><dc:identifier>https://doi.org/10.1002/jcb.28624</dc:identifier><dc:identifier>0730-2312</dc:identifier><dc:language>en</dc:language><dc:relation>Journal of Cellular Biochemistry</dc:relation><dc:rights>info:eu-repo/semantics/closedAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://munzur-rdlopen.rawdatalibrary.net/tr/items/munzur/3687</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>