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结直肠癌中抗死亡的病理生理机制。

Pathophysiological mechanisms of death resistance in colorectal carcinoma.

作者信息

Huang Ching-Ying, Yu Linda Chia-Hui

机构信息

Ching-Ying Huang, Linda Chia-Hui Yu, Graduate Institute of Physiology, National Taiwan University College of Medicine, Taipei 100, Taiwan.

出版信息

World J Gastroenterol. 2015 Nov 7;21(41):11777-92. doi: 10.3748/wjg.v21.i41.11777.

Abstract

Colon cancers develop adaptive mechanisms to survive under extreme conditions and display hallmarks of unlimited proliferation and resistance to cell death. The deregulation of cell death is a key factor that contributes to chemoresistance in tumors. In a physiological context, balance between cell proliferation and death, and protection against cell damage are fundamental processes for maintaining gut epithelial homeostasis. The mechanisms underlying anti-death cytoprotection and tumor resistance often bear common pathways, and although distinguishing them would be a challenge, it would also provide an opportunity to develop advanced anti-cancer therapeutics. This review will outline cell death pathways (i.e., apoptosis, necrosis, and necroptosis), and discuss cytoprotective strategies in normal intestinal epithelium and death resistance mechanisms of colon tumor. In colorectal cancers, the intracellular mechanisms of death resistance include the direct alteration of apoptotic and necroptotic machinery and the upstream events modulating death effectors such as tumor suppressor gene inactivation and pro-survival signaling pathways. The autocrine, paracrine and exogenous factors within a tumor microenvironment can also instigate resistance against apoptotic and necroptotic cell death in colon cancers through changes in receptor signaling or transporter uptake. The roles of cyclooxygenase-2/prostaglandin E2, growth factors, glucose, and bacterial lipopolysaccharides in colorectal cancer will be highlighted. Targeting anti-death pathways in the colon cancer tissue might be a promising approach outside of anti-proliferation and anti-angiogenesis strategies for developing novel drugs to treat refractory tumors.

摘要

结肠癌会形成适应性机制以在极端条件下存活,并表现出无限增殖和抗细胞死亡的特征。细胞死亡的失调是导致肿瘤化疗耐药的关键因素。在生理环境中,细胞增殖与死亡之间的平衡以及对细胞损伤的保护是维持肠道上皮稳态的基本过程。抗死亡细胞保护和肿瘤耐药的潜在机制通常具有共同的途径,尽管区分它们具有挑战性,但这也将为开发先进的抗癌疗法提供机会。本综述将概述细胞死亡途径(即凋亡、坏死和坏死性凋亡),并讨论正常肠上皮中的细胞保护策略以及结肠肿瘤的抗死亡机制。在结直肠癌中,抗死亡的细胞内机制包括凋亡和坏死性凋亡机制的直接改变以及调节死亡效应器的上游事件,如肿瘤抑制基因失活和促生存信号通路。肿瘤微环境中的自分泌、旁分泌和外源性因素也可通过受体信号传导或转运体摄取的变化,引发对结直肠癌凋亡和坏死性凋亡细胞死亡的抵抗。将重点介绍环氧合酶-2/前列腺素E2、生长因子、葡萄糖和细菌脂多糖在结直肠癌中的作用。针对结肠癌组织中的抗死亡途径可能是一种有前景的方法,有望在抗增殖和抗血管生成策略之外,开发治疗难治性肿瘤的新型药物。

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