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Overexpression of Proliferating Cell Nuclear Antigen in Mammalian Cells Negates Growth Arrest by Serum Starvation and Cell Contact

机译:哺乳动物细胞中增殖细胞核抗原的过表达通过血清饥饿和细胞接触抵消了生长停滞

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摘要

Proliferating cell nuclear antigen (PCNA) functions as a processivity factor for DNA polymerase δ, and is expressed at high levels in growing normal and tumor cells. To clarify the relationship between cell proliferation and PCNA expression, we generated NIH‐3T3 cells that overexpress PCNA and analyzed the phenotype of these cells. The resulting 3T3‐PCNA cells, which overexpressed PCNA, were found to proliferate beyond the saturation density of the parental NIH‐3T3 cells. Although NIH‐3T3 cell proliferation is arrested under serum starvation conditions, 3T3‐PCNA cell proliferation is not arrested by serum starvation. The expression levels of cdk2, cdk4 and cdk6 were the same in 3T3‐PCNA and NIH‐3T3 cells. The activity of cdk4 was identical for both cell types. However, the activity of cdk2 was higher in serum‐starved 3T3‐PCNA cells than in NIH‐3T3 cells, although the expression of cyclin E decreased in both types of cells, suggesting that increases in cdk2 activity are related to negation of growth arrest in 3T3‐PCNA cells. These results indicate that increases in PCNA expression lead to the disruption of growth control and may lead to malignant transformation.
机译:增殖细胞核抗原(PCNA)充当DNA聚合酶δ的合成因子,并在正在生长的正常细胞和肿瘤细胞中高水平表达。为了阐明细胞增殖与PCNA表达之间的关系,我们生成了过表达PCNA的NIH-3T3细胞并分析了这些细胞的表型。发现过度表达PCNA的3T3-PCNA细胞增殖超过亲本NIH-3T3细胞的饱和密度。尽管NIH-3T3细胞增殖在血清饥饿条件下被阻止,但3T3-PCNA细胞增殖并未被血清饥饿阻止。在3T3-PCNA和NIH-3T3细胞中,cdk2,cdk4和cdk6的表达水平相同。两种细胞类型的cdk4活性均相同。然而,尽管饥饿的3T3-PCNA细胞中cyclin E的表达在两种类型的细胞中均降低,但cdk2的活性却高于NIH-3T3细胞,这表明cdk2活性的增加与否定了生长停滞有关。 3T3-PCNA细胞。这些结果表明,PCNA表达的增加导致生长控制的破坏,并可能导致恶性转化。

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