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相关概念视频

Targeted Cancer Therapies02:57

Targeted Cancer Therapies

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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
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As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
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DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
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Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
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Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
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针对针对癌症治疗的可移植元素.

Yonghao Liang1,2, Xuan Qu1,2, Nakul M Shah3

  • 1Department of Genetics, Washington University School of Medicine, Saint Louis, MO, USA.

Nature reviews. Cancer
|January 16, 2024
PubMed
概括

可转移元素 (TE),曾经被称为"垃圾DNA",是癌症进化中的关键驱动因素. 了解它们的作用为癌症治疗提供了新的治疗点.

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科学领域:

  • 基因组学就是基因组学.
  • 癌症生物学 癌症生物学
  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.

背景情况:

  • 可转移元素 (TE) 占人类基因组的近一半.
  • 历史上被忽视为"垃圾DNA",TEs现在被认可为它们在基因调节,进化和疾病中的功能性作用.
  • 癌症的遗传和表观遗传景观是由TEs塑造的,影响癌症特异性基因活动.

研究的目的:

  • 审查可移植元素 (TE) 在癌症中的双重作用:促进其进化和提供治疗漏洞.
  • 讨论TE对转录组调节和癌症细胞过程的影响.
  • 突出特E作为新型癌症治疗的潜在目标.

主要方法:

  • 对癌症中可移植元素的当前文献的综述.
  • 对TEs对基因调节和癌症细胞过程的贡献的分析.
  • 讨论TE表征的基因组测试挑战.

主要成果:

  • 在癌症中,TEs充当"双刃剑",促进癌症的进展,同时呈现可利用的弱点.
  • 转录酶显著影响转录基因组调节和其他与癌症相关的细胞功能.
  • 基因组分析在全面描述TE时面临技术障碍.

结论:

  • 可转移的元素在癌症的发展和进展中发挥着关键的,多方面的作用.
  • 利用TE为创新的癌症治疗策略提供了有前途的途径.
  • 需要进一步的研究和改进的基因组技术,以充分理解和利用TEs在瘤学.