Regulation of signal transduction cascades by Pterostilbenes in different cancers: Is it a death knell for oncogenic pathways
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.
Anahtar Kelimeler
- Scopus
- 15
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Butt, Ghazala | |
| dc.contributor.author | Attar, Rukset | |
| dc.contributor.author | Tabassum, Sobia | |
| dc.contributor.author | Aras, Aliye | |
| dc.contributor.author | Qadir, Muhammad Imran | |
| dc.contributor.author | Ozbey, Ulku | |
| dc.contributor.author | Alaaeddine, Nada | |
| dc.contributor.author | Ozcelik, Beraat | |
| dc.contributor.author | Farooqi, Ammad Ahmad | |
| dc.date.accessioned | 2026-10-28T14:53:30.877232108Z | |
| dc.date.available | 2026-10-28T14:53:30.877232108Z | |
| dc.date.issued | 2017 | |
| dc.description.abstract | 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. | |
| dc.identifier.doi | 10.14715/cmb/2017.63.12.3 | |
| dc.identifier.eissn | 1165-158X | |
| dc.identifier.endpage | 10 | |
| dc.identifier.issn | 0145-5680 | |
| dc.identifier.issue | 12 | |
| dc.identifier.pmid | 29307345 | |
| dc.identifier.scopus | 2-s2.0-85039984196 | |
| dc.identifier.startpage | 5 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/munzur/658 | |
| dc.identifier.volume | 63 | |
| dc.identifier.wos | WOS:000419272800003 | |
| dc.language.iso | en | |
| dc.publisher | Cellular and Molecular Biology Association | |
| dc.relation.ispartof | Cellular and Molecular Biology | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Apoptosis | |
| dc.subject | Cancer | |
| dc.subject | MicroRNA | |
| dc.subject | Pterostilbene | |
| dc.subject | Signaling | |
| dc.subject | TRAIL | |
| dc.subject.other | Apoptosis | |
| dc.subject.other | Humans | |
| dc.subject.other | Janus Kinases | |
| dc.subject.other | MicroRNAs | |
| dc.subject.other | Neoplasms | |
| dc.subject.other | Receptors, Notch | |
| dc.subject.other | Signal Transduction | |
| dc.subject.other | STAT Transcription Factors | |
| dc.subject.other | Stilbenes | |
| dc.subject.other | Wnt Proteins | |
| dc.subject.other | metastasis associated protein 1 | |
| dc.subject.other | microRNA | |
| dc.subject.other | protein | |
| dc.subject.other | pterostilbene | |
| dc.subject.other | telomerase reverse transcriptase | |
| dc.subject.other | tumor necrosis factor related apoptosis inducing ligand | |
| dc.subject.other | unclassified drug | |
| dc.subject.other | Janus kinase | |
| dc.subject.other | Notch receptor | |
| dc.subject.other | STAT protein | |
| dc.subject.other | stilbene derivative | |
| dc.subject.other | Wnt protein | |
| dc.subject.other | mitogen activated protein kinase | |
| dc.subject.other | phosphatidylinositol 3 kinase | |
| dc.subject.other | protein kinase B | |
| dc.subject.other | cancer cell | |
| dc.subject.other | drug mechanism | |
| dc.subject.other | endoplasmic reticulum stress | |
| dc.subject.other | enzyme regulation | |
| dc.subject.other | gene expression | |
| dc.subject.other | human | |
| dc.subject.other | intracellular signaling | |
| dc.subject.other | JAK-STAT signaling | |
| dc.subject.other | malignant neoplasm | |
| dc.subject.other | MAPK signaling | |
| dc.subject.other | nonhuman | |
| dc.subject.other | Notch signaling | |
| dc.subject.other | pharmacokinetic parameters | |
| dc.subject.other | Pi3K/Akt signaling | |
| dc.subject.other | Review | |
| dc.subject.other | Wnt signaling | |
| dc.subject.other | drug effect | |
| dc.subject.other | metabolism | |
| dc.subject.other | neoplasm | |
| dc.subject.other | pathology | |
| dc.subject.other | carcinogenesis | |
| dc.subject.other | priority journal | |
| dc.subject.other | protein expression | |
| dc.subject.other | regulatory mechanism | |
| dc.subject.other | tumor suppressor gene | |
| dc.title | Regulation of signal transduction cascades by Pterostilbenes in different cancers: Is it a death knell for oncogenic pathways | |
| dc.type | Review Article | |
| rdl.citation.scopus | 15 | |
| rdl.department | Department of Botany, Government College University, Lahore, Katchery Road, Lahore 54000, Pakistan | |
| rdl.department | Department of Obstetrics and Gynecology, Yeditepe University Hospital Istanbul, Turkey | |
| rdl.department | Department of Bioinformatics and Biotechnology, International Islamic University, Islamabad 44000, Pakistan | |
| rdl.department | Department of Botany, Faculty of Science, Istanbul University, Istanbul 34460, Turkey | |
| rdl.department | Institute of Molecular Biology and Bio-technology, Bahauddin Zakariya University, Multan, Pakistan | |
| rdl.department | Department of Genetics, Health High School, Munzur University, 62000, Tunceli, Turkey | |
| rdl.department | Regenerative Medicine Laboratory, Faculty of Medicine, Saint-Joseph University, Beirut, Lebanon | |
| rdl.department | Food Engineering Department, Istanbul Technical University, Maslak, 34469, Istanbul, Turkey | |
| rdl.department | Laboratory for Translational Oncology and Personalized Medicine, Rashid Latif Medical College, Lahore, Pakistan | |
| rdl.oa.status | hybrid | |
| rdl.oa.status | closed | |
| rdl.oa.url | https://doi.org/10.14715/cmb/2017.63.12.3 | |
| rdl.scopus.quartile | Q3 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED |
