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Stable overexpression of PML alters regulation of cell cycle progression in HeLa cells
1Division of Laboratory Medicine, The University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Abstract:
Our previous studies demonstrated that PML is a growth suppressor that suppresses oncogenic transformation of NIH/3T3 cells and rat embryo fibroblasts. PML is a nuclear matrix-associated phosphoprotein whose expression is regulated during the cell cycle. Disruption of PML function by t(15;17) in acute promyelocytic leukemia (APL) plays a critical role in leukemogenesis. To further study the role of PML in the control of cell growth, we have stably overexpressed PML protein in the HeLa cell line. This overexpression of PML significantly reduced the growth rate of HeLa cells and suppressed anchorage-independent growth in soft agar. We consequently investigated several parameters correlated with cell growth and cell cycle progression. We found that, in comparison with the parental HeLa cells, HeLa/PML stable clones showed proportionally more cells in G1 phase, fewer cells in S phase and about the same number in G2/M phase. The HeLa/PML clones showed a significantly longer doubling time as a result of a lengthening of the G1 phase. No effect on apoptosis was found in HeLa cells overexpressing PML. This observation indicates that PML suppresses cell growth by increasing cell cycle duration as a result of G1 elongation. To further understand the mechanism of the effect of PML on HeLa cells, expression of cell cycle-related proteins in HeLa/PML and parental HeLa cells was analyzed. We found that Rb phosphorylation was significantly reduced in PML stable clones. Expression of cyclin E, Cdk2 and p27 proteins was also significantly reduced. These studies indicate that PML affects cell cycle progression by mediating expression of several key proteins that normally control cell cycle progression. These results further extend our current understanding of PML function in human cells and its important role in cell cycle regulation.
Insights
Promyelocytic leukemia (PML) protein acts as a growth suppressor by elongating the G1 phase of the cell cycle. Overexpression of PML in HeLa cells reduces growth rate and alters cell cycle protein expression.
Area of Science:
- Molecular Biology
- Cell Biology
- Cancer Research
Background:
- The promyelocytic leukemia (PML) protein is a known tumor suppressor involved in oncogenic transformation.
- PML is a nuclear phosphoprotein with cell cycle-regulated expression.
- Disruption of PML function is critical in acute promyelocytic leukemia (APL) pathogenesis.
Purpose of the Study:
- To investigate the role of PML in controlling cell growth and cell cycle progression.
- To analyze the effects of stable PML overexpression in the human HeLa cell line.
Main Methods:
- Stable overexpression of PML protein in HeLa cells.
- Analysis of cell growth rate, anchorage-independent growth, and cell cycle distribution.
- Western blot analysis of cell cycle-related proteins (Rb, cyclin E, Cdk2, p27).
Main Results:
- PML overexpression significantly reduced HeLa cell growth rate and anchorage-independent growth.
- HeLa/PML cells exhibited a longer G1 phase and increased doubling time.
- Reduced Rb phosphorylation and decreased expression of cyclin E, Cdk2, and p27 were observed in HeLa/PML cells.
- No significant effect on apoptosis was detected.
Conclusions:
- PML suppresses cell growth by prolonging the G1 phase of the cell cycle.
- PML influences cell cycle progression by regulating key cell cycle proteins.
- These findings enhance understanding of PML's function in human cells and cell cycle regulation.