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Apoptotic and autophagic pathways with relevant small‐molecule compounds,in cancer stem cells
Authors:Lan Zhang  Xupeng Tong  Jingjing Li  Yue Huang  Xinyue Hu  Yi Chen  Jian Huang  Jinhui Wang  Bo Liu
Institution:1. State Key Laboratory of Biotherapy/Collaborative Innovation Center of Biotherapy, West China Hospital, Sichuan University, Chengdu, China;2. School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China;3. School of Pharmacy, China Pharmaceutical University, Nanjing, China;4. Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, China
Abstract:Accumulating evidence demonstrates existence of cancer stem cells (CSCs), which are suspected of contributing to cancer cell self‐renewal capacity and resistance to radiation and/or chemotherapy. Including evasion of apoptosis and autophagic cell death, CSCs have revealed abilities to resist cell death, making them appealing targets for cancer therapy. Recently, molecular mechanisms of apoptosis and of autophagy in CSCs have been gradually explored, comparing them in stem cells and in cancer cells; distinct expression of these systems in CSCs may elucidate how these cells exert their capacity of unlimited self‐renewal and hierarchical differentiation. Due to their proposed ability to drive tumour initiation and progression, CSCs may be considered to be potentially useful pharmacological targets. Further, multiple compounds have been verified as triggering apoptosis and/or autophagy, suppressing tumour growth, thus providing new strategies for cancer therapy. In this review, we summarized regulation of apoptosis and autophagy in CSCs to elucidate how key proteins participate in control of survival and death; in addition, currently well‐studied compounds that target CSC apoptosis and autophagy are selectively presented. With increasing attention to CSCs in cancer therapy, researchers are now trying to find responses to unsolved questions as unambiguous as possible, which may provide novel insight into future anti‐cancer regimes.
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