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摘要:
Colorectal cancer is the second leading cause of death from cancer among adults. The disease begins as a benign adenomatous polyp, which develops into an advanced adenoma with high-grade dysplasia and then progresses to an invasive cancer. Appropriate apoptotic signaling is fundamentally important to preserve a healthy balance between cell death and cell survival and in maintaining genome integrity. Evasion of apoptotic pathway has been established as a prominent hallmark of several cancers. During colorectal cancer development, the balance between the rates of cell growth and apoptosis that maintains intestinal epithelial cell homeostasis gets progressively disturbed. Evidences are increasingly available to support the hypothesis that failure of apoptosis may be an important factor in the evolution of colorectal cancer and its poor response to chemotherapy and radiation. The other reason for targeting apoptotic pathway in the treatment of cancer is based on the observation that this process is deregulated in cancer cells but not in normal cells. As a result, colorectal cancer therapies designed to stimulate apoptosis in target cells would play a critical role in controlling its development and progression. A better understanding of the apoptotic signaling pathways, and the mechanisms by which cancer cells evade apoptotic death might lead to effective therapeutic strategies to inhibit cancer cell proliferation with minimal toxicity and high responses to chemotherapy. In this review, we analyzed the current understanding and future promises of apoptotic pathways as a therapeutic target in colorectal cancer treatment.
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篇名 Apoptotic pathways as a therapeutic target for colorectal cancer treatment
来源期刊 世界胃肠肿瘤学杂志:英文版(电子版) 学科 医学
关键词 COLORECTAL CANCER APOPTOTIC PATHWAYS DRUG resistance COLORECTAL CANCER THERAPIES Apoptosis
年,卷(期) 2016,(8) 所属期刊栏目
研究方向 页码范围 583-591
页数 9页 分类号 R735.34
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COLORECTAL
CANCER
APOPTOTIC
PATHWAYS
DRUG
resistance
COLORECTAL
CANCER
THERAPIES
Apoptosis
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世界胃肠肿瘤学杂志:英文版(电子版)
月刊
1948-5204
北京市朝阳区东四环中路62号楼远洋国际中
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664
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0
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