Hayashi Syunji, Ozaki Toshinori, Yoshida Kaori, Hosoda Mitsuchika, Todo Satoru, Akiyama Shin-ichi, Nakagawara Akira
Division of Biochemistry, Chiba Cancer Center Research Institute, Chuoh-ku, Japan.
Biochem Biophys Res Commun. 2006 Aug 18;347(1):60-6. doi: 10.1016/j.bbrc.2006.06.095. Epub 2006 Jun 27.
p73 responds to DNA damage and exerts its pro-apoptotic function. However, p73 might contribute to the development of drug-resistance in certain tumor cells. In this study, we found that p73 and MDM2 correlate with cisplatin-resistant phenotype of human epidermoid carcinoma-derived cells. p73 and MDM2 were kept at low levels in the cisplatin-sensitive KB-3-1 cells, whereas p53 was induced to be phosphorylated at Ser-15 in response to cisplatin. In contrast, p73 and MDM2 were expressed at higher levels, and cisplatin-mediated p53 phosphorylation was undetectable in the cisplatin-resistant KCP-4 cells. Enforced expression of p73 in KB-3-1 cells caused an accumulation of unphosphorylated form of p53 and MDM2, and conferred the cisplatin resistance. Collectively, our results suggest that a loss of the cisplatin sensitivity is at least in part due to a lack of cisplatin-induced p53 phosphorylation, and p73 might cooperate with MDM2 to be involved in this process.
p73对DNA损伤作出反应并发挥其促凋亡功能。然而,p73可能在某些肿瘤细胞中促进耐药性的发展。在本研究中,我们发现p73和MDM2与人类表皮样癌衍生细胞的顺铂耐药表型相关。在顺铂敏感的KB-3-1细胞中,p73和MDM2维持在低水平,而p53在顺铂作用下被诱导在Ser-15位点磷酸化。相反,在顺铂耐药的KCP-4细胞中,p73和MDM2表达水平较高,且未检测到顺铂介导的p53磷酸化。在KB-3-1细胞中强制表达p73导致未磷酸化形式的p53和MDM2积累,并赋予顺铂耐药性。总体而言,我们的结果表明,顺铂敏感性的丧失至少部分是由于缺乏顺铂诱导的p53磷酸化,并且p73可能与MDM2协同参与这一过程。