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OVA12 promotes tumor growth by regulating p53 expression in human cancer cells

机译:OVA12通过调节人癌细胞中的p53表达来促进肿瘤生长

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摘要

Ovarian cancer-associated antigen 12 (OVA12) was first identified in an ovarian carcinoma complementary DNA (cDNA) expression library and has been shown to play an important role in tumor growth. Here, we found that overexpression of OVA12 accelerated tumor growth in different tumor cells, whereas OVA12 depletion was associated with the opposite effect. Moreover, knocking down OVA12 led to a significant increase in the protein levels of p53, and the overexpression of OVA12 significantly decreased endogenous p53 levels. In addition, OVA12 stimulated p53 polyubiquitination and degradation by the proteasome and promoted tumor growth at least partially through the p53 pathway. Taken together, these results indicate that OVA12 is a negative regulator of p53 and that inhibition of OVA12 expression might serve as a therapeutic target to restore tumor suppression.
机译:卵巢癌相关抗原12(OVA12)首先在卵巢癌互补DNA(cDNA)表达文库中鉴定,并已显示在肿瘤生长中起重要作用。在这里,我们发现OVA12的过表达促进了不同肿瘤细胞中肿瘤的生长,而OVA12的消耗与相反的作用有关。此外,敲除OVA12导致p53蛋白水平显着增加,而OVA12的过表达显着降低了内源性p53水平。另外,OVA12通过蛋白酶体刺激p53多聚泛素化和降解,并至少部分通过p53途径促进肿瘤生长。综上所述,这些结果表明OVA12是p53的负调节剂,并且OVA12表达的抑制可能用作恢复肿瘤抑制的治疗靶标。

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