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Vascular endothelial growth factor encoded by Parapoxviruses can regulate metabolism and survival of triple negative breast cancer cells

机译:由ParaPoxviruses编码的血管内皮生长因子可以调节三元阴性乳腺癌细胞的代谢和存活

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Dysbiotic microbiomes are linked to many pathological outcomes including different metabolic disorders like diabetes, atherosclerosis and even cancer. Breast cancer is the second leading cause of cancer associated death in women, and triple negative breast cancer (TNBC) is the most aggressive type with major challenges for intervention. Previous reports suggested that Parapoxvirus signatures are one of the predominant dysbiotic viral signatures in TNBC. These viruses encode several genes that are homologs of human genes. In this study, we show that the VEGF homolog encoded by Parapoxviruses, can induce cell proliferation, and alter metabolism of breast cancer and normal breast cells, through alteration of MAPK-ERK and PI3K-AKT signaling. In addition, the activity of the transcription factor FoxO1 was altered by viral-encoded VEGF through activation of the PI3K-AKT pathway, leading to reprogramming of cellular metabolic gene expression. Therefore, this study provides new insights into the function of viral-encoded VEGFs, which promoted the growth of the breast cancer cells and imparted proliferative phenotype with altered metabolism in normal breast cells.
机译:疑难生微生物胶质瘤与许多病理结果相关联,包括糖尿病,动脉粥样硬化甚至癌症等不同代谢障碍。乳腺癌是癌症相关死亡的第二个主要原因,而三重阴性乳腺癌(TNBC)是最具侵略性的类型,具有治疗干预的主要挑战。以前的报道表明,ParaPoxvirus签名是TNBC中主要的歧疲力病病毒签名之一。这些病毒编码了几种是人类基因同源物的基因。在这项研究中,我们表明,通过Papk-ERK和PI3K-AKT信号传导的改变,通过ParaPoxviruses编码的VEGF同源物可以诱导细胞增殖和乳腺癌和正常乳腺细胞的代谢。此外,通过激活PI3K-AKT途径通过病毒编码的VEGF改变转录因子FoxO1的活性,从而导致细胞代谢基因表达的重编程。因此,该研究为病毒编码的VEGF的功能提供了新的见解,该功能促进了乳腺癌细胞的生长,并赋予正常乳腺细胞中的代谢改变了增殖表型。

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