Xie Hua, Wang Hao
Department of Thoracic Oncology, Sichuan Cancer Hospital, Chengdu, Sichuan 610041, P.R. China.
Department of Breast Surgery, Sichuan Cancer Hospital, Chengdu, Sichuan 610041, P.R. China.
Oncol Lett. 2018 Mar;15(3):2795-2800. doi: 10.3892/ol.2017.7639. Epub 2017 Dec 19.
Prior studies have demonstrated that phosphatase of regenerating liver-3 (PRL-3) serves avital function in cell proliferation and metastasis in breast cancer. However, the molecular mechanisms underlying the function of PRL-3 in breast cancer remain unknown. PRL-3 expression was analyzed in 24 pairs of breast cancer and normal tissues using the reverse transcription-quantitative polymerase chain reaction assay. The results of the present study identified that the expression of PLR-3 in breast cancer tissues was increased 4.2-fold, compared with normal tissues. Notably, overexpression of PRL-3 significantly promoted the proliferation of cancer cells and inhibited endogenous p53 expression by downregulating the expression level of p14 alternate reading frame (p14). In addition, decreased expression levels of PRL-3 resulted in decreased breast cancer cell proliferation and increased expression level of p14. These results suggested that PRL-3 enhances cell proliferation by downregulating p14 expression, which results in decreased levels ofp53. The results of the present study demonstrated that PRL-3 promotes tumor proliferation by affecting the p14-p53 axis, and that it may serve as a prognostic marker for patients with breast cancer.
先前的研究表明,再生肝脏磷酸酶3(PRL-3)在乳腺癌细胞增殖和转移中发挥着重要作用。然而,PRL-3在乳腺癌中发挥作用的分子机制仍不清楚。采用逆转录-定量聚合酶链反应分析24对乳腺癌组织和正常组织中PRL-3的表达情况。本研究结果表明,与正常组织相比,乳腺癌组织中PLR-3的表达增加了4.2倍。值得注意的是,PRL-3的过表达显著促进癌细胞增殖,并通过下调p14可变阅读框(p14)的表达水平抑制内源性p53表达。此外,PRL-3表达水平降低导致乳腺癌细胞增殖减少和p14表达水平增加。这些结果表明,PRL-3通过下调p14表达来增强细胞增殖,从而导致p53水平降低。本研究结果表明,PRL-3通过影响p14-p53轴促进肿瘤增殖,并且它可能作为乳腺癌患者的预后标志物。