Regulation of signal transduction cascades by Pterostilbenes in different cancers: Is it a death knell for oncogenic pathways

Derleme MakaleAçık ErişimScopus SJRQ3

Özet

Interdisciplinary research has revolutionized the field of medicine and we have witnessed exponential increase in the high-impact research in past few decades. However, the road to this burgeoning research field is obstacle-ridden because of intratumor heterogeneity, loss of apoptosis and dysregulation of spatio-temporally controlled signaling pathways. Ground-breaking findings obtained through genetic, genomic and proteomic studies have considerably improved our concepts related to the complexity of protein network and excitingly, discovery of miRNAs has added another layer of intricacy to quantitatively regulated gene networks. In this review, we chronicle the milestone achievements and discuss how Pterostilbenes effectively regulated different cellular pathways. We have provided detailed mechanistic insights related to regulation of JAK-STAT signaling, Notch pathway, Wnt mediated intracellular signaling by pterostilbene. Underlying mechanisms about regulation of PI3K/AKT and MAPK pathways by pterostilbene in different cancers. Regulation of Metastasis-associated protein 1 (MTA1) proteins and Human telomerase reverse transcriptase (hTERT) in cancer cells by pterostilbene. Pterostilbene has also been reported to modulate the expression of various oncogenic and tumor suppressor microRNAs in cancer cells. Better and sharper comprehension of the concepts associated with the modes of action of pterostilbene in different cancers will be useful in identification of cancers which can be efficiently targeted by pterostilbene.

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/munzur/658Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.14715/cmb/2017.63.12.3Yayıncı resmi DOI adresi
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorButt, Ghazala
dc.contributor.authorAttar, Rukset
dc.contributor.authorTabassum, Sobia
dc.contributor.authorAras, Aliye
dc.contributor.authorQadir, Muhammad Imran
dc.contributor.authorOzbey, Ulku
dc.contributor.authorAlaaeddine, Nada
dc.contributor.authorOzcelik, Beraat
dc.contributor.authorFarooqi, Ammad Ahmad
dc.date.accessioned2026-10-28T14:53:30.877232108Z
dc.date.available2026-10-28T14:53:30.877232108Z
dc.date.issued2017
dc.description.abstractInterdisciplinary research has revolutionized the field of medicine and we have witnessed exponential increase in the high-impact research in past few decades. However, the road to this burgeoning research field is obstacle-ridden because of intratumor heterogeneity, loss of apoptosis and dysregulation of spatio-temporally controlled signaling pathways. Ground-breaking findings obtained through genetic, genomic and proteomic studies have considerably improved our concepts related to the complexity of protein network and excitingly, discovery of miRNAs has added another layer of intricacy to quantitatively regulated gene networks. In this review, we chronicle the milestone achievements and discuss how Pterostilbenes effectively regulated different cellular pathways. We have provided detailed mechanistic insights related to regulation of JAK-STAT signaling, Notch pathway, Wnt mediated intracellular signaling by pterostilbene. Underlying mechanisms about regulation of PI3K/AKT and MAPK pathways by pterostilbene in different cancers. Regulation of Metastasis-associated protein 1 (MTA1) proteins and Human telomerase reverse transcriptase (hTERT) in cancer cells by pterostilbene. Pterostilbene has also been reported to modulate the expression of various oncogenic and tumor suppressor microRNAs in cancer cells. Better and sharper comprehension of the concepts associated with the modes of action of pterostilbene in different cancers will be useful in identification of cancers which can be efficiently targeted by pterostilbene.
dc.identifier.doi10.14715/cmb/2017.63.12.3
dc.identifier.eissn1165-158X
dc.identifier.endpage10
dc.identifier.issn0145-5680
dc.identifier.issue12
dc.identifier.pmid29307345
dc.identifier.scopus2-s2.0-85039984196
dc.identifier.startpage5
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/658
dc.identifier.volume63
dc.identifier.wosWOS:000419272800003
dc.language.isoen
dc.publisherCellular and Molecular Biology Association
dc.relation.ispartofCellular and Molecular Biology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectApoptosis
dc.subjectCancer
dc.subjectMicroRNA
dc.subjectPterostilbene
dc.subjectSignaling
dc.subjectTRAIL
dc.subject.otherApoptosis
dc.subject.otherHumans
dc.subject.otherJanus Kinases
dc.subject.otherMicroRNAs
dc.subject.otherNeoplasms
dc.subject.otherReceptors, Notch
dc.subject.otherSignal Transduction
dc.subject.otherSTAT Transcription Factors
dc.subject.otherStilbenes
dc.subject.otherWnt Proteins
dc.subject.othermetastasis associated protein 1
dc.subject.othermicroRNA
dc.subject.otherprotein
dc.subject.otherpterostilbene
dc.subject.othertelomerase reverse transcriptase
dc.subject.othertumor necrosis factor related apoptosis inducing ligand
dc.subject.otherunclassified drug
dc.subject.otherJanus kinase
dc.subject.otherNotch receptor
dc.subject.otherSTAT protein
dc.subject.otherstilbene derivative
dc.subject.otherWnt protein
dc.subject.othermitogen activated protein kinase
dc.subject.otherphosphatidylinositol 3 kinase
dc.subject.otherprotein kinase B
dc.subject.othercancer cell
dc.subject.otherdrug mechanism
dc.subject.otherendoplasmic reticulum stress
dc.subject.otherenzyme regulation
dc.subject.othergene expression
dc.subject.otherhuman
dc.subject.otherintracellular signaling
dc.subject.otherJAK-STAT signaling
dc.subject.othermalignant neoplasm
dc.subject.otherMAPK signaling
dc.subject.othernonhuman
dc.subject.otherNotch signaling
dc.subject.otherpharmacokinetic parameters
dc.subject.otherPi3K/Akt signaling
dc.subject.otherReview
dc.subject.otherWnt signaling
dc.subject.otherdrug effect
dc.subject.othermetabolism
dc.subject.otherneoplasm
dc.subject.otherpathology
dc.subject.othercarcinogenesis
dc.subject.otherpriority journal
dc.subject.otherprotein expression
dc.subject.otherregulatory mechanism
dc.subject.othertumor suppressor gene
dc.titleRegulation of signal transduction cascades by Pterostilbenes in different cancers: Is it a death knell for oncogenic pathways
dc.typeReview Article
rdl.citation.scopus15
rdl.departmentDepartment of Botany, Government College University, Lahore, Katchery Road, Lahore 54000, Pakistan
rdl.departmentDepartment of Obstetrics and Gynecology, Yeditepe University Hospital Istanbul, Turkey
rdl.departmentDepartment of Bioinformatics and Biotechnology, International Islamic University, Islamabad 44000, Pakistan
rdl.departmentDepartment of Botany, Faculty of Science, Istanbul University, Istanbul 34460, Turkey
rdl.departmentInstitute of Molecular Biology and Bio-technology, Bahauddin Zakariya University, Multan, Pakistan
rdl.departmentDepartment of Genetics, Health High School, Munzur University, 62000, Tunceli, Turkey
rdl.departmentRegenerative Medicine Laboratory, Faculty of Medicine, Saint-Joseph University, Beirut, Lebanon
rdl.departmentFood Engineering Department, Istanbul Technical University, Maslak, 34469, Istanbul, Turkey
rdl.departmentLaboratory for Translational Oncology and Personalized Medicine, Rashid Latif Medical College, Lahore, Pakistan
rdl.oa.statushybrid
rdl.oa.statusclosed
rdl.oa.urlhttps://doi.org/10.14715/cmb/2017.63.12.3
rdl.scopus.quartileQ3
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED