Department of Biology, Texas Southern University, Houston, TX 77004, USA.
Department of Environmental and Interdisciplinary Sciences, Texas Southern University, Houston, TX 77004, USA.
Int J Mol Sci. 2024 Feb 22;25(5):2539. doi: 10.3390/ijms25052539.
The MYBL1 gene is a strong transcriptional activator involved in events associated with cancer progression. Previous data show MYBL1 overexpressed in triple-negative breast cancer (TNBC). There are two parts to this study related to further characterizing the MYBL1 gene. We start by characterizing MYBL1 reference sequence variants and isoforms. The results of this study will help in future experiments in the event there is a need to characterize functional variants and isoforms of the gene. In part two, we identify and validate expression and gene-related alterations of MYBL1, VCIP1, MYC and BOP1 genes in TNBC cell lines and patient samples selected from the Breast Invasive Carcinoma TCGA 2015 dataset available at cBioPortal.org. The four genes are located at chromosomal regions 8q13.1 to 8q.24.3 loci, regions previously identified as demonstrating a high percentage of alterations in breast cancer. We identify alterations, including changes in expression, deletions, amplifications and fusions in MYBL1, VCPIP1, BOP1 and MYC genes in many of the same patients, suggesting the panel of genes is involved in coordinated activity in patients. We propose that MYBL1, VCPIP1, MYC and BOP1 collectively be considered as genes associated with the chromosome 8q loci that potentially play a role in TNBC pathogenesis.
MYBL1 基因是一种强有力的转录激活因子,参与与癌症进展相关的事件。先前的数据表明,MYBL1 在三阴性乳腺癌(TNBC)中过表达。本研究有两个部分,涉及进一步描述 MYBL1 基因。我们首先描述 MYBL1 参考序列变异体和异构体。本研究的结果将有助于未来的实验,以便对该基因的功能变异体和异构体进行特征描述。在第二部分中,我们在从 cBioPortal.org 上可获得的 Breast Invasive Carcinoma TCGA 2015 数据集的 TNBC 细胞系和患者样本中鉴定和验证 MYBL1、VCIP1、MYC 和 BOP1 基因的表达和基因相关改变。这四个基因位于染色体 8q13.1 到 8q24.3 位点,这些区域先前被确定为乳腺癌中改变百分比较高的区域。我们在许多相同的患者中鉴定出改变,包括 MYBL1、VCPIP1、BOP1 和 MYC 基因的表达变化、缺失、扩增和融合,这表明该基因面板参与了患者的协调活动。我们提出,MYBL1、VCPIP1、MYC 和 BOP1 可被视为与染色体 8q 位点相关的基因,这些基因可能在 TNBC 发病机制中发挥作用。