Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, and Department of Medicine, Brigham & Women's Hospital, Boston, MA 02215, USA.
Gastroenterology. 2011 Jul;141(1):50-61. doi: 10.1053/j.gastro.2011.05.010.
Survival times of patients with colorectal cancer (CRC) have increased over the past decade, primarily as a result of treatment with combinations of conventional cytotoxic agents. Because CRC is commonly associated with mutations in genes that control growth factor signaling, therapies are being developed to target the products of these genes; individualized treatment might also be guided by specific mutations in tumors and by new biomarkers. Currently, targeted therapies confer limited clinical benefit; better drugs are therefore needed. Genomic studies indicate that phosphoinositide 3-kinase (PI3K) signaling is one of the most frequently deregulated pathways in several human cancers, including CRC. PI3K signaling has an important role in cancer cell proliferation, survival, motility, and metabolism and therefore could be an attractive therapeutic target. We review PI3K signaling in CRC and discuss current therapeutic approaches.
过去十年中,结直肠癌(CRC)患者的生存时间有所延长,主要是由于常规细胞毒性药物联合治疗的结果。由于 CRC 通常与控制生长因子信号的基因发生突变有关,因此正在开发针对这些基因产物的治疗方法;个体化治疗也可能受到肿瘤中特定突变和新生物标志物的指导。目前,靶向治疗带来的临床获益有限;因此,需要更好的药物。基因组研究表明,磷脂酰肌醇 3-激酶(PI3K)信号是包括 CRC 在内的多种人类癌症中最常失调的途径之一。PI3K 信号在癌细胞增殖、存活、运动和代谢中具有重要作用,因此可能是一个有吸引力的治疗靶点。我们综述了结直肠癌中的 PI3K 信号,并讨论了当前的治疗方法。