دورية أكاديمية

Human Homeobox TGIFLX Regulates CDX1, CDX2, and OCT1 Genes Expression in Colorectal Cancer Cell Lines

التفاصيل البيبلوغرافية
العنوان: Human Homeobox TGIFLX Regulates CDX1, CDX2, and OCT1 Genes Expression in Colorectal Cancer Cell Lines
المؤلفون: Soroosh Shahryarhesami, Mansour Heidari, Masoud Heidari, Nahid Sadighi
المصدر: Middle East Journal of Cancer, Vol 13, Iss 2, Pp 216-225 (2022)
بيانات النشر: Shiraz University of Medical Sciences, 2022.
سنة النشر: 2022
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: colorectal neoplasms, homeobox genes, rna, small interfering, mutation, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Background: Homeodomain transcriptional regulatory proteins, which are encoded by Homeobox (HOX) genes, play critical roles in both normal development and carcinogenesis. Previous studies have shown that the expression of HOX genes is deregulated in numerous tumors and this expression is specific to each cancer based on the arising embryonic origin tissue and the site of tumor. Method: In this in vitro study, the expression levels of HOXA10, CDX1, CDX2, TGIFLX, TGIFLY, and OCT1 genes were compared across 10 different human colorectal cancer cell lines with different differentiation stages. Subsequently, the effect of TGIFLX siRNA-mediated knockdown on the expression levels of CDX1, CDX2, and OCT1 genes was analyzed in SW948 cell line. Results: The obtained results revealed that these homeobox genes were differentially expressed in different colorectal cancer cell lines. Furthermore, the siRNA-mediated knockdown of TGIFLX led to higher levels of CDX1, CDX2, and OCT1 expression. Conclusion: Our data suggested that TGIFLX plays an important role in the upstream regulation of CDX1, CDX2, and OCT1 genes.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2008-6709
2008-6687
Relation: https://mejc.sums.ac.ir/article_47623_fe48601a9be70c4689680438374f947b.pdf; https://doaj.org/toc/2008-6709; https://doaj.org/toc/2008-6687
DOI: 10.30476/mejc.2021.86467.1345
URL الوصول: https://doaj.org/article/25d34d6731be42c08ac22ad4468a1703
رقم الأكسشن: edsdoj.25d34d6731be42c08ac22ad4468a1703
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20086709
20086687
DOI:10.30476/mejc.2021.86467.1345