癌症研究的历史:逆转录病毒插入性突变发生
1Departments of Pathology, Genetics, and Biology, Stanford University, Stanford, California 94305-5324, USA lipsick@stanford.edu.
Cold Spring Harbor perspectives in biology
|July 5, 2023
概括
复原病毒可以通过插入性突变发生引起癌症,其中病毒DNA激活细胞原型瘤基因. 这一发现揭示了新的瘤基因和瘤抑制剂,影响了早期的基因治疗研究.
科学领域:
- 在瘤学瘤学.
- 病毒学 病毒学
- 分子生物学分子生物学
背景情况:
- 早期的癌症研究在一些逆转录病毒中发现了促进瘤发生的瘤基因.
- 无基因逆转录病毒引起癌症的机制尚不清楚.
- 原型瘤基因是细胞基因,当异常表达时,可以促进癌症.
研究的目的:
- 审查癌症中逆转录病毒插入性突变发生的历史发现.
- 解释病毒序列如何激活内源原型瘤基因.
- 讨论识别新瘤基因,瘤抑制剂和基因疗法的影响.
主要方法:
- 20世纪80年代科学文献的历史综述.
- 对癌症发展中的逆转录病毒机制研究的分析.
- 检查对瘤基因和瘤抑制基因发现的影响.
主要成果:
- 发现插入性突变发生作为无基因逆转录病毒的致癌机制.
- 发现病毒序列驱动细胞原瘤基因的异常表达.
- 从这些研究中发现了新型瘤基因和瘤抑制基因.
结论:
- 逆转录病毒的插入性突变发生是癌症发展的一个重要机制.
- 这种现象扩大了对瘤发生和瘤抑制的理解.
- 这些发现突出了与早期基因治疗方法相关的风险.
相关概念视频
Mechanisms of Retrovirus-induced Cancers
5.1K
Retroviruses are RNA viruses that have been shown to cause cancers in diverse species, including chickens, mice, cats, and monkeys. The RNA genomes of these viruses are first reverse-transcribed into single and then double-stranded DNA (dsDNA) copies. This dsDNA called proviral DNA then integrates into the host genome. Subsequently, the host cell transcribes the proviral DNA in concert with the chromosomal DNA. This leads to the production of viral RNA and proteins that assemble at the host...
5.1K
Rous Sarcoma Virus (RSV) and Cancer
5.1K
Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
RSV is a retrovirus that contains two copies of a plus-strand RNA genome. Its genome consists of four main open...
5.1K
Retroviruses
12.4K
Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
12.4K
Non-LTR Retrotransposons
11.6K
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...
11.6K
In-vitro Mutagenesis
14.0K
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
14.0K
Mutagenicity and Carcinogenicity
1.3K
Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...
1.3K


