Ahmadiankia Naghmeh, Bagheri Mehdi, Fazli Mozhgan
School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran.
Cancer Prevention Research Center, Shahroud University of Medical Sciences, Shahroud, Iran.
Rep Biochem Mol Biol. 2019 Jul;8(2):139-146.
Breast cancer is the leading cause of cancer related death in women worldwide. The development of metastatic cancer is the main factor contributing to mortality. The molecular mechanisms underlying the metastatic process have yet to be clearly elucidated. However, the interplay between the tumor microenvironment and the cancer cells hold a critical role in influencing the progression of cancer metastasis. Within the microenvironment of solid tumors, the lack of sufficient vasculature leads to the development of nutrient deprived conditions. This study aimed to examine how nutrient deprivation influences factors involved in cancer progression and metastasis. Specifically, we examined how nutrient stress changes cancer cell migration, the gene expression, and cytokine production of metastasis-related factors in a human breast cancer cell line.
MCF7 breast cancer cells were cultured in serum-free media for 24, 48, and 72 h. Cell migration was evaluated using a transwell migration assay. The transcriptional expression of metastatic related genes was examined via real-time PCR. Cytokine production was examined via enzyme-linked immunosorbent assay.
Nutrient deprivation of the MCF7 cells significantly reduced cell migration after 24 h. However, following 72 h of nutrient deprivation, there was significant increase in cell migration compared to the 24 h group. Transcriptional expression of markers involved in migration including, β-catenin, twist, vimentin, fibronectin, ICAM1, VCAM1, and VEGF were up regulated after 72 h of nutrient deprivation. The cytokines TGFβ1, IL-8, and MCP1 were differentially secreted.
Nutrient deprivation is an environmental stress factor that can influence the behavior of cancer cells. Current treatments implement nutrient deprivation as a potential cancer treatment. Under short periods of nutrient deprivation, cancer cell migration is inhibited. However, our findings show that following extended lengths of nutrient deprivation, cancer cells are capable of adapting themselves to the environmental condition and restoring their migratory abilities. This, in part, may be a result of increased expression of metastasis-related genes. Further research is required to accurately identify how the expression of metastasis-related genes is modulated and controlled in response to nutrient deprivation and environmental stress.
乳腺癌是全球女性癌症相关死亡的主要原因。转移性癌症的发展是导致死亡的主要因素。转移过程背后的分子机制尚未完全阐明。然而,肿瘤微环境与癌细胞之间的相互作用在影响癌症转移进程中起着关键作用。在实体瘤的微环境中,缺乏足够的脉管系统会导致营养缺乏状况的出现。本研究旨在探讨营养缺乏如何影响参与癌症进展和转移的因素。具体而言,我们研究了营养应激如何改变人乳腺癌细胞系中癌细胞的迁移、转移相关因子的基因表达和细胞因子产生。
MCF7乳腺癌细胞在无血清培养基中培养24、48和72小时。使用Transwell迁移试验评估细胞迁移。通过实时PCR检测转移相关基因的转录表达。通过酶联免疫吸附测定检测细胞因子产生。
MCF7细胞营养缺乏24小时后显著降低细胞迁移。然而,营养缺乏72小时后,与24小时组相比细胞迁移显著增加。营养缺乏72小时后,参与迁移的标志物β-连环蛋白、扭曲蛋白、波形蛋白、纤连蛋白、细胞间黏附分子1、血管细胞黏附分子1和血管内皮生长因子的转录表达上调。细胞因子转化生长因子β1、白细胞介素-8和单核细胞趋化蛋白-1的分泌存在差异。
营养缺乏是一种可影响癌细胞行为的环境应激因素。目前的治疗方法将营养缺乏作为一种潜在的癌症治疗手段。在短期营养缺乏情况下,癌细胞迁移受到抑制。然而,我们的研究结果表明,在长期营养缺乏后,癌细胞能够适应环境条件并恢复其迁移能力。这部分可能是转移相关基因表达增加的结果。需要进一步研究以准确确定转移相关基因的表达如何响应营养缺乏和环境应激而被调节和控制。