Song Lanxi, Turkson James, Karras James G, Jove Richard, Haura Eric B
Experimental Therapeutics, H. Lee Moffitt Cancer Center and Research Insitute, University of South Florida College of Medicine Tampa, FL 33612, USA.
Oncogene. 2003 Jul 3;22(27):4150-65. doi: 10.1038/sj.onc.1206479.
Overexpression of receptor tyrosine kinases including the epidermal growth factor receptor (EGF-R) as well as nonreceptor tyrosine kinases, such as Src, have been implicated in the formation of human lung cancers. In addition, cytokines like interleukin-6 (IL-6) have been demonstrated to modulate lung cancer cell growth and elevated levels of IL-6 have been shown to be an adverse prognostic factor for patients with lung cancer. Despite a large body of evidence pointing to their potential importance, few direct studies into the role of signal transducers and activators of transcription (STAT) pathways in human lung cancer have been undertaken. Here we demonstrate that multiple nonsmall cell lung cancer cell lines demonstrate constitutive Stat3 DNA-binding activity. Stat3 DNA-binding activity is specifically upregulated by the addition of epidermal growth factor (EGF), IL-6, and hepatocyte-derived growth factor (HGF). Furthermore, the stimulation of Stat3 DNA-binding activity by EGF requires the activity of EGF-R tyrosine kinase as well as Src-kinase, while the upregulation of Stat3 activity by IL-6 or HGF requires only Src-kinase activity. Treatment of A549 lung cancer cells with PD180970 or SU6656, both pharmacological inhibitors of Src-kinase, resulted in reduced Src and Stat3 activity, cell cycle arrest in G2, and reduced viability of cells accompanied by induction of apoptosis. Treatment of Stat3-positive A549 and H358 cells with antisense Stat3 oligonucleotides results in complete loss of Stat3 DNA-binding activity and apoptosis, while Stat3-positive H1299 cells remained healthy. Finally, an adenoviral vector expressing a dominant-negative Stat3 isoform results in loss of Stat3 DNA-binding activity, apoptosis, and reduced cellular viability. These results demonstrate a role of Stat3 in transducing survival signals downstream of tyrosine kinases such as Src, EGF-R, and c-Met, as well as cytokines such as IL-6, in human nonsmall cell lung cancers.
包括表皮生长因子受体(EGF-R)在内的受体酪氨酸激酶以及非受体酪氨酸激酶(如Src)的过表达与人类肺癌的形成有关。此外,诸如白细胞介素-6(IL-6)等细胞因子已被证明可调节肺癌细胞的生长,并且IL-6水平升高已被证明是肺癌患者的不良预后因素。尽管有大量证据表明它们具有潜在重要性,但针对信号转导与转录激活因子(STAT)通路在人类肺癌中的作用的直接研究却很少。在此我们证明,多种非小细胞肺癌细胞系表现出组成性的Stat3 DNA结合活性。通过添加表皮生长因子(EGF)、IL-6和肝细胞衍生生长因子(HGF)可特异性上调Stat3 DNA结合活性。此外,EGF对Stat3 DNA结合活性的刺激需要EGF-R酪氨酸激酶以及Src激酶的活性,而IL-6或HGF对Stat3活性的上调仅需要Src激酶活性。用Src激酶的两种药理抑制剂PD180970或SU6656处理A549肺癌细胞,导致Src和Stat3活性降低、细胞周期停滞在G2期,细胞活力降低并伴有凋亡诱导。用反义Stat3寡核苷酸处理Stat3阳性的A549和H358细胞会导致Stat3 DNA结合活性完全丧失和凋亡,而Stat3阳性的H1299细胞则保持健康。最后,表达显性负性Stat3异构体的腺病毒载体导致Stat3 DNA结合活性丧失、凋亡和细胞活力降低。这些结果证明了Stat3在转导酪氨酸激酶(如Src、EGF-R和c-Met)以及细胞因子(如IL-6)下游的存活信号中在人类非小细胞肺癌中的作用。