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3-溴丙酮酸抑制肿瘤糖酵解和促进细胞凋亡 被引量:1

3-bromopyruvate inhibites of tumor glycolysis and promotion of apoptosis
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摘要 肿瘤细胞的生长所需的能量主要来自糖酵解产生的三磷酸腺苷(adenosine triphosphate,ATP)。基于该理论,国内外大量研究者对肿瘤能量代谢相关靶点展开研究。近年来不断有研究指出,3-溴丙酮酸(3-bromopyruvate,3-BrPA)作为一种烷化剂,具有抗肿瘤作用,其机制可能是对糖酵解关键酶起到抑制作用,从而阻断肿瘤的能量来源、诱导活性氧产生,最终促进肿瘤细胞凋亡,且对肿瘤周围的组织器官没有影响;也有相关研究发现:3-BrPA可逆转肿瘤细胞耐药性、增强光敏剂疗效和提高肿瘤细胞对抗癌药物敏感性。因此,3-BrPA有望成为一种高效、低毒的抗肿瘤药物。本文通过调研国内外关于3-BrPA相关实验的研究,对3-BrPA抑制肿瘤细胞糖代谢和促进肿瘤细胞凋亡的可能机制进行探讨,以期为抗肿瘤药物研究提供一定帮助。 Considering that the energy required for tumor cell growth mainly comes from adenosine triphosphate(ATP)produced by the aerobic glycolysis,various investigations have been carried out on tumor energy metabolism related targets.In recent years,3-bromopyruvate(3-BrPA),a strong alkylating agent,has been reported to have anti-tumor effects.The mechanism may be to inhibit the key enzymes of glycolysis,so as to block the energy source of tumor,which induces the production of reactive oxygen species,and finally leads to the apoptosis of tumor cells without affecting the tissues and organs around the tumor.Moreover,some studies have reported that 3-BrPA reversed tumor cell drug resistance,enhanced the efficacy of photosensitizers and improved the sensitivity of tumor cells to anticancer drugs.Therefore,3-BrPA is expected to be a highly efficient anti-tumor agent with low-toxicity.In this paper,based on our investigations and researches on studies concerning 3-BrPA at home and aboard,we discussed the possible mechanism of 3-BrPA in terms of inhibiting glucose metabolism of tumor cells and promoting tumor cell apoptosis,in the hope of providing some help for the study of anti-tumor drugs.
作者 潘建民 罗小辉 杨成 肖旺发 李其尚 张晓东 PAN Jianmin;LUO Xiaohui;YANG Cheng;XIAO Wangfa;LI Qishang;ZHANG Xiaodong(Department of Gastrointestinal Glandular Surgery,The First Affiliated Hospital of Guangxi Medical University,Nanning 530000,China)
出处 《生命的化学》 CAS 2022年第8期1461-1469,共9页 Chemistry of Life
基金 国家自然科学基金项目(81760476)。
关键词 3-溴丙酮酸 糖酵解 己糖激酶 活性氧 凋亡 3-bromopyruvate glycolysis hexokinase reactive oxygen species c-Myc apoptosis
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  • 1Nakajima EC, Van Houten B. Metabolic symbiosis in cancer: refocusing the Warburg lens. Mol Carcinog, 2012,52:329-337. 被引量:1
  • 2Ho J, de Moura MB, Lin Y, et al. Importance of glycolysis and oxidative phosphorylation in advanced melanoma. Mol Cancer, 2012,11:76-88. 被引量:1
  • 3Warburg O. On the origin of cancer cells. Science, 1956,123:309- 314. 被引量:1
  • 4Scott DA, Richardson AD, Filipp FV, et al. Comparative metabolic flux profiling of melanoma cell lines: beyond the Warburg effect. J Blot Chem, 2011,286:42626-42634. 被引量:1
  • 5Gatenby RA, Gillies RJ. Why do cancers have high aerobic glycolysis? Nat Rev Cancer, 2004, 4: 891-899. 被引量:1
  • 6Shime H, Yabu M, Akazawa T, et al. Tumor-secreted lactic acid promotes IL-23/IL-17 proinflammatory pathway. J Immunol, 2008,180:7175-7183. 被引量:1
  • 7Vegran F, , Boidot R, Michiels C, et al. Lactate influx through theendothelial cell monocarboxylate transporter MCT1 supports an NF-KB/IL-8 pathway that drives tumor angiogenesis. Cancer Res, 2011,71:2550-2560. 被引量:1
  • 8Hirschhaeuser F, Sattler UG, Mueller-Klieser W. Lactate: a metabolic key player in cancer. Cancer Res, 2011,71:6921-6925. 被引量:1
  • 9Walenta S, Mueller-Klieser WF, Lactate: mirror and motor of tumor malignancy. Semin Radiat Oncol, 2004,14:267-274. 被引量:1
  • 10Balch CM, Gershenwald JE, Soong S J, et al. Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol, 2009,27:6199-6206. 被引量:1

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