Panneerselvam Janani, Munshi Anupama, Ramesh Rajagopal
Department of Pathology, Stanton L Young Biomedical Research Center, The University of Oklahoma Health Sciences Center, Suite 1403, 975 NE 10th, Oklahoma City, OK 73104, USA.
J Mol Signal. 2013 Dec 30;8(1):15. doi: 10.1186/1750-2187-8-15.
Cancer remains a major health issue in the world and the effectiveness of current therapies is limited resulting in disease recurrence and resistance to therapy. Therefore to overcome disease recurrence and have improved treatment efficacy there is a continued effort to develop and test new anticancer drugs that are natural or synthetic - (conventional chemotherapeutics, small molecule inhibitors) and biologic (antibody, tumor suppressor genes, oligonucleotide) product. In parallel, efforts for identifying molecular targets and signaling pathways to which cancer cells are "addicted" are underway. By inhibiting critical signaling pathways that is crucial for cancer cell survival, it is expected that the cancer cells will undergo a withdrawal symptom akin to "de-addiction" resulting in cell death. Thus, the key for having an improved and greater control on tumor growth and metastasis is to develop a therapeutic that is able to kill tumor cells efficiently by modulating critical signaling pathways on which cancer cells rely for their survival.Currently several small molecule inhibitors targeted towards unique molecular signaling pathways have been developed and tested in the clinic. Few of these inhibitors have shown efficacy while others have failed. Thus, targeting a single molecule or pathway may be insufficient to completely block cancer cell proliferation and survival. It is therefore important to identify and test an anticancer drug that can inhibit multiple signaling pathways in a cancer cell, control growth of both primary and metastatic tumors and is safe.One biologic agent that has the characteristics of serving as a potent anticancer drug is interleukin (IL)-24. IL-24 suppresses multiple signaling pathways in a broad-spectrum of human cancer cells leading to tumor cell death, inhibition of tumor angiogenesis and metastasis. Additionally, combining IL-24 with other therapies demonstrated additive to synergistic antitumor activity. Clinical testing of IL-24 as a gene-based therapeutic for the treatment of solid tumors demonstrated that IL-24 is efficacious and is safe. The unique features of IL-24 support its further development as an anticancer drug for cancer treatment.In this review we summarize the current understanding on the molecular targets and signaling pathways regulated by IL-24 in mediating its anticancer activity.
癌症仍然是全球主要的健康问题,当前治疗方法的有效性有限,导致疾病复发和对治疗产生抗性。因此,为了克服疾病复发并提高治疗效果,人们持续致力于研发和测试新型抗癌药物,这些药物包括天然或合成的(传统化疗药物、小分子抑制剂)以及生物制剂(抗体、肿瘤抑制基因、寡核苷酸)产品。与此同时,识别癌细胞“依赖”的分子靶点和信号通路的工作也在进行中。通过抑制对癌细胞存活至关重要的关键信号通路,有望使癌细胞出现类似于“脱瘾”的戒断症状,从而导致细胞死亡。因此,更好地控制肿瘤生长和转移的关键在于开发一种能够通过调节癌细胞赖以生存的关键信号通路来有效杀死肿瘤细胞的疗法。目前,针对独特分子信号通路的几种小分子抑制剂已被研发并在临床中进行测试。其中少数抑制剂显示出疗效,而其他的则失败了。因此,仅靶向单个分子或通路可能不足以完全阻断癌细胞的增殖和存活。所以,识别和测试一种能够抑制癌细胞中多种信号通路、控制原发性和转移性肿瘤生长且安全的抗癌药物非常重要。白细胞介素(IL)-24是一种具有作为强效抗癌药物特征的生物制剂。IL-24可抑制多种人类癌细胞中的信号通路,导致肿瘤细胞死亡、抑制肿瘤血管生成和转移。此外,将IL-24与其他疗法联合使用显示出相加至协同的抗肿瘤活性。将IL-24作为基于基因的疗法用于实体瘤治疗的临床试验表明,IL-24有效且安全。IL-24的独特特性支持其作为抗癌药物进一步开发用于癌症治疗。在本综述中,我们总结了目前对IL-24在介导其抗癌活性过程中所调控的分子靶点和信号通路的认识。