Author/Authors :
Ahmadiankia, Naghmeh School of Medicine - Shahroud University of Medical Sciences, Iran , Bagheri, Mehdi Imam Hossein Hospital - Clinical Research Development UnitShahroud - University of Medical Sciences, Iran , Fazli, Mozhgan School of Medicine - Shahroud University of Medical Sciences, Iran
Abstract :
Background: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.
Methods:MCF7 breast cancer cells were cultured in serum-free media for 24, 48, and 72 h. Cell migration was
evaluated using a transwellmigration assay. The transcriptional expression of metastatic related genes was
examined via real-time PCR. Cytokine production was examined via enzyme-linked immunosorbent assay.
Results: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.
Conclusions: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.