0
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      铁死亡的分子机制及其对膀胱癌的影响 Translated title: Molecular mechanisms of ferroptosis and its effects on bladder cancer

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          膀胱癌(bladder cancer,BC)是泌尿系统三大常见恶性肿瘤之一,具有发病率高、易转移、治疗效果不佳、预后较差的特点,严重威胁着全人类的健康。肿瘤细胞表现出强烈的需铁现象,而铁超载会诱导细胞发生铁死亡,即一种由脂质过氧化和细胞膜损伤引起的铁依赖性细胞死亡。因此,铁死亡具有很强的抗肿瘤潜力。铁死亡的分子机制与细胞磷脂代谢异常、铁代谢异常、抗氧化和非抗氧化系统Xc -/谷胱甘肽(glutathione,GSH)/谷胱甘肽过氧化物酶4(glutathione peroxidase 4,GPX4)的失调有关。铁死亡相关分子在BC的发生和发展、转移、耐药及免疫反应等方面发挥着重要的作用,有望成为治疗BC的靶点。

          Translated abstract

          Bladder cancer (BC) is one of the 3 common malignant tumors in the urinary system, with high incidence, easy metastasis, poor therapeutic efficacy, and poor prognosis, which seriously threatens the health of human. Tumor cells exhibit a strong demand for iron, and iron overload can induce ferroptosis, which is an iron dependent cell death caused by lipid peroxidation and cell membrane damage. Therefore, ferroptosis has strong anti-tumor potential. The molecular mechanisms of ferroptosis is associated with abnormalities in cellular phospholipid metabolism and iron metabolism, and dysregulation of antioxidant and non-antioxidant systems Xc -/glutathione (GSH)/glutathione peroxidase 4 (GPX4). Ferroptosis relevant molecules play important roles in the occurrence and development, metastasis, drug resistance, and immune response of BC, and are expected to become targets for the treatment of BC.

          Related collections

          Most cited references76

          • Record: found
          • Abstract: found
          • Article: not found

          Ferroptosis: an iron-dependent form of nonapoptotic cell death.

          Nonapoptotic forms of cell death may facilitate the selective elimination of some tumor cells or be activated in specific pathological states. The oncogenic RAS-selective lethal small molecule erastin triggers a unique iron-dependent form of nonapoptotic cell death that we term ferroptosis. Ferroptosis is dependent upon intracellular iron, but not other metals, and is morphologically, biochemically, and genetically distinct from apoptosis, necrosis, and autophagy. We identify the small molecule ferrostatin-1 as a potent inhibitor of ferroptosis in cancer cells and glutamate-induced cell death in organotypic rat brain slices, suggesting similarities between these two processes. Indeed, erastin, like glutamate, inhibits cystine uptake by the cystine/glutamate antiporter (system x(c)(-)), creating a void in the antioxidant defenses of the cell and ultimately leading to iron-dependent, oxidative death. Thus, activation of ferroptosis results in the nonapoptotic destruction of certain cancer cells, whereas inhibition of this process may protect organisms from neurodegeneration. Copyright © 2012 Elsevier Inc. All rights reserved.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Targeting Ferroptosis to Iron Out Cancer

            One of the key challenges in cancer research is how to effectively kill cancer cells while leaving the healthy cells intact. Cancer cells often have defects in cell death executioner mechanisms, which is one of the main reasons for therapy resistance. To enable growth, cancer cells exhibit an increased iron demand compared with normal, non-cancer cells. This iron dependency can make cancer cells more vulnerable to iron-catalyzed necrosis, referred to as ferroptosis. The identification of FDA-approved drugs as ferroptosis inducers creates high expectations for the potential of ferroptosis to be a new promising way to kill therapy-resistant cancers.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              DHODH-mediated ferroptosis defence is a targetable vulnerability in cancer

                Bookmark

                Author and article information

                Journal
                Zhong Nan Da Xue Xue Bao Yi Xue Ban
                Zhong Nan Da Xue Xue Bao Yi Xue Ban
                zndx
                Journal of Central South University Medical Sciences
                中南大学出版社 (湖南省长沙市湘雅路110号湘雅医学院 )
                1672-7347
                28 February 2024
                : 49
                : 2
                : 286-295
                Affiliations
                [1] [1 ] 甘肃中医药大学第一临床医学院 兰州 730000 [1 ] First School of Clinical Medical, Gansu University of Chinese Medicince Lanzhou 730000
                [2] [2 ] 中国人民解放军联勤保障部队第九四〇医院泌尿外科 兰州 730050 [2 ] Department of Urology, 940th Hospital of Joint Logistic Support Force of Chinese People’s Liberation Army Lanzhou 730050
                [3] [3 ] 甘肃省干细胞与基因药物重点实验室 兰州 730050 [3 ] Gansu Provincial Key Laboratory of Stem Cell and Gene Drug Lanzhou 730050 China
                Author notes
                杨旭凯,Email: yangxk125@ 123456126.com , ORCID: 0000-0003-0617-3247

                李瑞杰,Email: 1786420780@ 123456qq.com , ORCID: 0009-0007-5195-185X

                Article
                1672-7347(2024)02-0286-10 230352
                10.11817/j.issn.1672-7347.2024.230352
                11103069
                38755725
                98833cad-f716-4bbc-86be-498262e70fa5
                ©Journal of Central South University (Medical Science). All rights reserved.

                开放获取 (Open access):本文遵循知识共享许可协议,允许第三方用户按照署名-非商业性使用-禁止演绎4.0(CC BY-NC-ND 4.0)的方式,在任何媒介以任何形式复制、传播本作品( https://creativecommons.org/licenses/by-nc-nd/4.0/)。

                History
                : 20 August 2023
                Funding
                Funded by: 甘肃省自然科学基金
                Award ID: 21JR11RA008
                Funded by: 兰州市人才创新创业项目
                Award ID: 2021-RC-106┫。This work was supported by the Natural Science Foundation of Gansu Province ┣21JR11RA008
                Funded by: the Talent Innovation and Entrepreneurship Program of Lanzhou
                Award ID: 2021-RC-106
                Categories
                Reviews

                膀胱癌,铁死亡,脂质过氧化,磷脂代谢,铁代谢,xc-/谷胱甘肽/谷胱甘肽过氧化物酶4,铁死亡相关分子,bladder cancer,ferroptosis,lipid peroxidation,phospholipid metabolism,iron metabolism,xc-/glutathione/glutathione peroxidase 4,ferroptosis relevant molecules

                Comments

                Comment on this article