TY - JOUR
T1 - The role of prospero homeobox 1 (PROX1) expression in follicular thyroid carcinoma cells
AU - Rudzinska, Magdalena
AU - Ledwon, Joanna Karolina
AU - Gawel, Damian
AU - Sikorska, Justyna
AU - Czarnocka, Barbara
N1 - Funding Information:
This work was supported by grant 2012/07/B/ NZ5/02444 from The National Science Center, Poland. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
PY - 2017
Y1 - 2017
N2 - The prospero homeobox 1 (Prox1) transcription factor is a key player during embryogenesis and lymphangiogenesis. Altered Prox1 expression has been found in a variety of human cancers, including papillary thyroid carcinoma (PTC). Interestingly, Prox1 may exert tumor suppressive or tumor promoting effect, depending on the tissue context. In this study, we have analyzed Prox1 expression in normal and malignant human thyroid carcinoma cell lines. Moreover, we determined the effect of Prox1 silencing and overexpression on the cellular processes associated with the metastatic potential of tumor cells: proliferation, migration, invasion, apoptosis and anchorageindependent growth, in the follicular thyroid carcinoma (FTC) FTC-133 cell line. We found that Prox1 expression was significantly higher in FTC-derived cells than in PTCderived cells and normal thyroid, and it was associated with the PI3K/Akt signaling pathway. In the FTC-133 cells, it was associated with cell invasive potential, motility and wound closure capacities, but not with proliferation or apoptosis. Modifying Prox1 expression also induced substantial changes in the cytoskeleton structure and cell morphology. In conclusion, we have shown that Prox1 plays an important role in the development of FTC and that its suppression prevents, whereas its overexpression promotes, the malignant behavior of thyroid follicular cancer cells.
AB - The prospero homeobox 1 (Prox1) transcription factor is a key player during embryogenesis and lymphangiogenesis. Altered Prox1 expression has been found in a variety of human cancers, including papillary thyroid carcinoma (PTC). Interestingly, Prox1 may exert tumor suppressive or tumor promoting effect, depending on the tissue context. In this study, we have analyzed Prox1 expression in normal and malignant human thyroid carcinoma cell lines. Moreover, we determined the effect of Prox1 silencing and overexpression on the cellular processes associated with the metastatic potential of tumor cells: proliferation, migration, invasion, apoptosis and anchorageindependent growth, in the follicular thyroid carcinoma (FTC) FTC-133 cell line. We found that Prox1 expression was significantly higher in FTC-derived cells than in PTCderived cells and normal thyroid, and it was associated with the PI3K/Akt signaling pathway. In the FTC-133 cells, it was associated with cell invasive potential, motility and wound closure capacities, but not with proliferation or apoptosis. Modifying Prox1 expression also induced substantial changes in the cytoskeleton structure and cell morphology. In conclusion, we have shown that Prox1 plays an important role in the development of FTC and that its suppression prevents, whereas its overexpression promotes, the malignant behavior of thyroid follicular cancer cells.
KW - Cytoskeleton
KW - Follicular thyroid carcinoma
KW - Invasion
KW - PROX1
KW - Thyroid cancer
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U2 - 10.18632/oncotarget.23167
DO - 10.18632/oncotarget.23167
M3 - Article
C2 - 29371975
AN - SCOPUS:85039053649
VL - 8
SP - 114136
EP - 114155
JO - Oncotarget
JF - Oncotarget
SN - 1949-2553
IS - 69
ER -