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A systemic approach to cancer treatment: Tumor cell reprogramming focused on endocrine-related cancers

机译:癌症治疗的系统方法:肿瘤细胞重编程重点关注内分泌相关癌症

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The term "cancer cell reprogramming" is used to define any kind of intervention aimed at transforming cancer cells into terminally differentiated cells. Using this approach, new technologies have been applied with different methods for a more systemic approach to cancer treatment. This review reports on advances of these technologies, including our personal contributions, mainly carried out on endocrine-related cancers. Some of the interventions, aimed at reverting cancer cells into a normal phenotype, are based on the evidence that tumor development is suppressed by the embryonic microenvironment. On the basis of this rationale, experiments have been conducted using stem cell differentiation stage factors (SCDSFs) taken at different stages of development of Zebrafish embryos, oocyte extracts, or na?ve human umbilical cord matrix derived stem cells (UMDSCs). SCDSFs induce significant growth inhibition on different tumor cell lines in vitro, likely because of increases in cell cycle regulatory molecules, such as p53 and pRb. Treatment with these factors activates apoptosis and differentiation related to caspase-3. This is achieved via p73 apoptotic-dependent pathway activation with a concurrent normalization of the E-cadherin and beta-catenin ratio. Extracts from prophase amphibian oocytes could reprogram relevant epigenetic alterations in MCF-7 and HCC1954 breast cancer cell lines, while un-engineered (na?ve) human UMDSCs attenuated growth of MDA-231 human breast carcinoma cells. A product prepared for human treatments, containing SCDSFs at very low doses, yielded favorable results in breast cancer and in intermediate-advanced hepatocellular carcinoma. Other reprogramming interventions used in the models of breast, prostate and ovarian cancer cell lines are described. Finally, current and future perspectives of this novel technology are discussed and a new hallmark of cancer is suggested: the loss of differentiation of cancer cells.
机译:术语“癌细胞重编程”用于定义旨在将癌细胞转化成末端分化细胞的任何类型的干预。使用这种方法,已经用不同方法应用了新技术,以获得更具系统性癌症治疗方法。本次审查关于这些技术的进度报告,包括我们的个人贡献,主要针对内分泌相关癌症。旨在将癌细胞恢复到正常表型的一些干预措施,基于胚胎微环境抑制肿瘤发育的证据。在该理由的基础上,使用斑马鱼胚胎,卵母细胞提取物或Naαve人脐脊基质衍生干细胞(UMDSCs)的不同阶段进行的实验使用干细胞分化阶段因子(SCDSF)进行了实验。 SCDSF在体外对不同肿瘤细胞系诱导显着的生长抑制,可能因为细胞周期调节分子(例如P53和PRB)的增加。用这些因素治疗激活与Caspase-3相关的细胞凋亡和分化。这通过P73凋亡依赖性途径激活来实现,并经常归一化E-Cadherin和β-连环蛋白比率。来自预壳两栖动物卵母细胞的提取物可以重新编程MCF-7和HCC1954乳腺癌细胞中相关的表观遗传改变,而未经工程化(Na'Ve)人uMDSCs减弱MDA-231人乳腺癌细胞的生长。为人类治疗制备的产品,含有非常低剂量的SCDSF,产生乳腺癌和中期晚期肝细胞癌的良好结果。描述了乳腺,前列腺和卵巢癌细胞系模型中使用的其他重编程干预。最后,讨论了这种新技术的当前和未来的观点,并提出了一种新的癌症标志:癌细胞的分化丧失。

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