Investigation of alterations in PIK3CA and OCT-4 gene expression in breast cancer
Özet
Breast cancer (BCa) is one of the most prevalent cancer amongst women and PIK3CA mutations have a crucial role in carcinogenesis. On the other hand, Octamer-Binding Transcription Factor 4 (OCT-4) is common biomarkers of cancer stem cells, which provide to the pathological processes of numerous carcinomas. In this study, we evaluated the association of OCT-4 gene expression levels with the PIK3CA mutation in BCa patients. The mRNA expression level of the OCT-4 gene was detected by qPCR in 44 BCa patients and 30 BCa patients control have positive PIK3CA mutations. Exon 9 and exon 20 of PIK3CA mutations were identified by sequencing. OCT-4 gene expression and PIK3CA mutations were also clinically evaluated in BCa patients. The frequency of PIK3CA mutation in 44 new cases were 32%. PIK3CA mutations were significantly associated with HER2-positive (p = 0.0271) status, Ki-67 status (p = 0.0434) and patient age (p = 0.0149). OCT-4 mRNA expression was significantly higher in the BCa tissue in comparison to normal breast tissue (p = 0.0305). A significant correlation was found between expression of OCT-4 and node status (p = 0.0190). OCT-4 mRNA expression was higher in the PIK3CA mutation tissue than the wild type tissue. However, no association was found between the expression of OCT-4 and the PIK3CA mutation or wild type samples (p = 0.7908). Our results provided that OCT-4 gene and PIK3CA mutations may have a role in development of BCa. OCT-4 mRNA expression level and PIK3CA mutations have a potential important for BCa diagnosis or treatment.
Anahtar Kelimeler
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- OpenAlex
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Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Dirican, Ebubekir | |
| dc.contributor.author | Kankaya, Burak | |
| dc.contributor.author | Büyükaşık, Süleyman | |
| dc.contributor.author | Alış, Halil | |
| dc.contributor.author | Velidedeoğlu, Mehmet | |
| dc.contributor.author | İlvan, Sennur | |
| dc.contributor.author | İlvan, Ahmet | |
| dc.date.accessioned | 2026-10-29T19:10:47.771046154Z | |
| dc.date.available | 2026-10-29T19:10:47.771046154Z | |
| dc.date.issued | 2020 | |
| dc.description.abstract | Breast cancer (BCa) is one of the most prevalent cancer amongst women and PIK3CA mutations have a crucial role in carcinogenesis. On the other hand, Octamer-Binding Transcription Factor 4 (OCT-4) is common biomarkers of cancer stem cells, which provide to the pathological processes of numerous carcinomas. In this study, we evaluated the association of OCT-4 gene expression levels with the PIK3CA mutation in BCa patients. The mRNA expression level of the OCT-4 gene was detected by qPCR in 44 BCa patients and 30 BCa patients control have positive PIK3CA mutations. Exon 9 and exon 20 of PIK3CA mutations were identified by sequencing. OCT-4 gene expression and PIK3CA mutations were also clinically evaluated in BCa patients. The frequency of PIK3CA mutation in 44 new cases were 32%. PIK3CA mutations were significantly associated with HER2-positive (p = 0.0271) status, Ki-67 status (p = 0.0434) and patient age (p = 0.0149). OCT-4 mRNA expression was significantly higher in the BCa tissue in comparison to normal breast tissue (p = 0.0305). A significant correlation was found between expression of OCT-4 and node status (p = 0.0190). OCT-4 mRNA expression was higher in the PIK3CA mutation tissue than the wild type tissue. However, no association was found between the expression of OCT-4 and the PIK3CA mutation or wild type samples (p = 0.7908). Our results provided that OCT-4 gene and PIK3CA mutations may have a role in development of BCa. OCT-4 mRNA expression level and PIK3CA mutations have a potential important for BCa diagnosis or treatment. | |
| dc.description.sponsorship | Istanbul Aydın University | |
| dc.description.sponsorship | Research Foundation of Istanbul Ayd?n University | |
| dc.description.sponsorship | British Association for Psychopharmacology, BAP | |
| dc.identifier.articlenumber | 100942 | |
| dc.identifier.doi | 10.1016/j.genrep.2020.100942 | |
| dc.identifier.eissn | 2452-0144 | |
| dc.identifier.issn | 2452-0144 | |
| dc.identifier.scopus | 2-s2.0-85094956501 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/bayburt/13326 | |
| dc.identifier.volume | 21 | |
| dc.identifier.wos | WOS:000598178300012 | |
| dc.language.iso | en | |
| dc.publisher | Elsevier Inc. | |
| dc.relation.ispartof | Gene Reports | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Biomarker | |
| dc.subject | Breast cancer | |
| dc.subject | OCT-4 | |
| dc.subject | PIK3CA | |
| dc.subject | qPCR | |
| dc.subject.classification | Genetics & Heredity | |
| dc.subject.other | octamer transcription factor 4 | |
| dc.subject.other | phosphatidylinositol 4,5 bisphosphate 3 kinase | |
| dc.subject.other | phosphatidylinositol 4,5 bisphosphate 3 kinase catalytic subunit alpha | |
| dc.subject.other | unclassified drug | |
| dc.subject.other | Article | |
| dc.subject.other | breast cancer | |
| dc.subject.other | breast tissue | |
| dc.subject.other | cancer patient | |
| dc.subject.other | cancer staging | |
| dc.subject.other | controlled study | |
| dc.subject.other | exon | |
| dc.subject.other | female | |
| dc.subject.other | gene mutation | |
| dc.subject.other | genetic association | |
| dc.subject.other | human | |
| dc.subject.other | human epidermal growth factor receptor 2 positive breast cancer | |
| dc.subject.other | human tissue | |
| dc.subject.other | major clinical study | |
| dc.subject.other | mRNA expression level | |
| dc.subject.other | priority journal | |
| dc.subject.other | real time polymerase chain reaction | |
| dc.title | Investigation of alterations in PIK3CA and OCT-4 gene expression in breast cancer | |
| dc.type | Article | |
| rdl.citation.openalex | 1 | |
| rdl.citation.scopus | 1 | |
| rdl.citation.wos | 1 | |
| rdl.oa.status | closed | |
| rdl.oa.status | green | |
| rdl.oa.url | http://hdl.handle.net/20.500.12403/3412 | |
| rdl.scopus.quartile | Q4 | |
| rdl.sdg | SDG03 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.wos.index | Emerging Sources Citation Index (ESCI) |

