Qiao Liang, Wong Benjamin C Y
Department of Medicine and Centre for Cancer Research, The University of Hong Kong, Hong Kong.
Drug Resist Updat. 2009 Jun;12(3):55-64. doi: 10.1016/j.drup.2009.02.002. Epub 2009 Mar 10.
Cancers in the gastrointestinal system account for a large proportion of malignancies and cancer-related deaths with gastric cancer and colorectal cancer being the most common ones. For those patients in whom surgical resection is not possible, other therapeutic approaches are necessary. Disordered apoptosis has been linked to cancer development and treatment resistance. Apoptosis occurs via extrinsic or intrinsic signaling each triggered and regulated by many different molecular pathways. In recent years, the selective induction of apoptosis in tumor cells has been increasingly recognized as a promising approach for cancer therapy. A detailed understanding of the molecular pathways involved in the regulation of apoptosis is essential for developing novel effective therapeutic approaches. Apoptosis can be induced by many different approaches including activating cell surface death receptors (for example, Fas, TRAIL and TNF receptors), inhibiting cell survival signaling (such as EGFR, MAPK and PI3K), altering apoptosis threshold by modulating pro-apoptotic and anti-apoptotic members of the Bcl-2 family, down-regulating anti-apoptosis proteins (such as XIAP, survivin and c-IAP2), and using other pro-apoptotic agents. In this review, the authors reviewed the currently reported apoptosis-targeting approaches in gastrointestinal cancers.
胃肠道系统癌症在恶性肿瘤及癌症相关死亡中占很大比例,其中胃癌和结直肠癌最为常见。对于那些无法进行手术切除的患者,需要其他治疗方法。细胞凋亡紊乱与癌症发生及治疗耐药性有关。细胞凋亡通过外在或内在信号传导发生,每种信号传导都由许多不同的分子途径触发和调节。近年来,选择性诱导肿瘤细胞凋亡越来越被认为是一种有前景的癌症治疗方法。详细了解参与细胞凋亡调节的分子途径对于开发新的有效治疗方法至关重要。细胞凋亡可通过多种不同方法诱导,包括激活细胞表面死亡受体(如Fas、TRAIL和TNF受体)、抑制细胞存活信号传导(如EGFR、MAPK和PI3K)、通过调节Bcl-2家族的促凋亡和抗凋亡成员改变凋亡阈值、下调抗凋亡蛋白(如XIAP、survivin和c-IAP2)以及使用其他促凋亡剂。在本综述中,作者回顾了目前报道的胃肠道癌症中针对细胞凋亡的方法。