Department of Medicine, University of Chicago, Chicago, IL, USA.
Cancer Biol Ther. 2010 Mar 15;9(6):409-16. doi: 10.4161/cbt.9.6.11233. Epub 2010 Mar 18.
Lung cancer is the leading cause of cancer deaths worldwide. Small cell lung cancer (SCLC), which comprises 15% of all lung cancers, is almost exclusively due to smoking and is highly aggressive due to early widespread metastasis. While combination chemotherapy has lead to modest improvements in outcome, the five-year overall survival for SCLC remains at 5%. Identifying distinct biochemical pathways of metastasis and chemotherapy resistance in SCLC may lead to novel therapeutic approaches and improve survival in SCLC patients. The chemokine receptor CXCR4 is emerging as an important target in cancer growth, metastasis, relapse and resistance to therapy. In this article, we review the structure and function of CXCR4 and its ligand, CXCL12, as well as mechanisms of CXCR4/CXCL12 signal transduction in lung cancer. We review the current preclinical and translational research involving this pathway in lung cancer and the clinical development of several novel agents targeting the CXCR4/CXCL12 pathway. Further understanding of the CXCR4/CXCL12 pathway in SCLC and NSCLC may provide a rationale for innovative research on the CXCR4 receptor as a potential novel therapeutic target in lung cancer.
肺癌是全球癌症死亡的主要原因。小细胞肺癌(SCLC)约占所有肺癌的 15%,几乎完全由吸烟引起,由于早期广泛转移,其侵袭性很强。虽然联合化疗已导致 SCLC 患者的结局略有改善,但 SCLC 的五年总生存率仍保持在 5%。确定 SCLC 中转移和化疗耐药的不同生化途径可能会导致新的治疗方法,并改善 SCLC 患者的生存。趋化因子受体 CXCR4 作为癌症生长、转移、复发和对治疗的耐药性的一个重要靶点正在出现。本文综述了 CXCR4 及其配体 CXCL12 的结构和功能,以及 CXCR4/CXCL12 信号转导在肺癌中的机制。本文还综述了涉及该途径的目前的临床前和转化研究,以及几种靶向 CXCR4/CXCL12 途径的新型药物的临床开发。进一步了解 SCLC 和 NSCLC 中的 CXCR4/CXCL12 途径,可能为 CXCR4 受体作为肺癌潜在的新治疗靶点的创新性研究提供依据。