Pham Thu-Huyen, Park Hyo-Min, Kim Jinju, Hong Jin Tae, Yoon Do-Young
Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Korea.
College of Pharmacy and Medical Research Center, Chungbuk National University, Chungbuk 28160, Korea.
Biomedicines. 2020 Dec 21;8(12):637. doi: 10.3390/biomedicines8120637.
The tumor suppressor p53 is considered the "guardian of the genome" that can protect cells against cancer by inducing cell cycle arrest followed by cell death. However, STAT3 is constitutively activated in several human cancers and plays crucial roles in promoting cancer cell proliferation and survival. Hence, STAT3 and p53 have opposing roles in cellular pathway regulation, as activation of STAT3 upregulates the survival pathway, whereas p53 triggers the apoptotic pathway. Constitutive activation of STAT3 and gain or loss of p53 function due to mutations are the most frequent events in numerous cancer types. Several studies have reported the association of STAT3 and/or p53 mutations with drug resistance in cancer treatment. This review discusses the relationship between STAT3 and p53 status in cancer, the molecular mechanism underlying the negative regulation of p53 by STAT3, and vice versa. Moreover, it underlines prospective therapies targeting both STAT3 and p53 to enhance chemotherapeutic outcomes.
肿瘤抑制因子p53被视为“基因组守护者”,它可通过诱导细胞周期停滞继而引发细胞死亡来保护细胞免受癌症侵害。然而,信号转导及转录激活因子3(STAT3)在多种人类癌症中持续激活,并在促进癌细胞增殖和存活方面发挥关键作用。因此,STAT3和p53在细胞通路调节中具有相反作用,因为STAT3的激活会上调存活通路,而p53则触发凋亡通路。STAT3的持续激活以及因突变导致的p53功能获得或丧失是众多癌症类型中最常见的事件。多项研究报道了STAT3和/或p53突变与癌症治疗中的耐药性之间的关联。本综述讨论了癌症中STAT3和p53状态之间的关系、STAT3对p53进行负调控的分子机制,反之亦然。此外,它强调了针对STAT3和p53两者的前瞻性疗法,以提高化疗效果。