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烟草烟雾致癌物导致DNA修复机制功能丧失:碳纳米管的保护作用。

Tobacco Smoke Carcinogens Induce DNA Repair Machinery Function Loss: Protection by Carbon Nanotubes.

作者信息

Dhasmana Anukriti, Dhasmana Anupam, H Hobani Yahya, Farasani Abdullah, Habibullah Mahmoud, Alshammary Freah L, Khan Saif, Haque Shafiul, Lohani Mohtashim

机构信息

Himalayan School of Biosciences, Swami Rama Himalayan University, Dehradun (Uttarakhand), India.

University of Texas Rio Grande Valley, McAllen, United States of America.

出版信息

Asian Pac J Cancer Prev. 2020 Oct 1;21(10):3099-3108. doi: 10.31557/APJCP.2020.21.10.3099.

DOI:10.31557/APJCP.2020.21.10.3099
PMID:33112573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7798159/
Abstract

PURPOSE

DNA damage is a continuous process occurring within the cells caused by intrinsic and extrinsic factors, but it gets repaired regularly. If the DNA repair process is faulty, the incidences of damages/mutations can accumulate in cells resulting in cell transformation. It is hypothesized that the negative variations in DNA repair pathways in even at one point viz. genetic, translational or posttranslational stage may fairly be crucial for the beginning and development of carcinogenesis. Therefore, we investigated the potential of tobacco specific nitrosamines (TSNs) related carcinogens to interact with the enzymes involved in DNA repair mechanisms in the current study.

METHODS

The derivatives of cigarettes' smoke like NNK and NNAL are very well known and recognized carcinogens. Therefore, almost 120 enzymes playing crucial role in the DNA repair process have been analysed for their reactivity with NNK and NNAL.

RESULTS

The molecular docking study helped to screen out,  07 possible DNA repair enzyme targets for NNK, and 12for NNAL. Present study revealed the loss of activity of DNA repair enzymes in the presence of NNK and NNAL, and this accumulation may induce the tendency of DNA damage which can lead the transformation of exposed normal cells in to cancerous cells. This study also demonstrated the protective potential of nanoparticles like SWCNTs/MWCNTs against TSN's induced toxicity; here SWCNT against NNK (-17.16 Kcal/Mol) and MWCNT against NNK -17.01 Kcal/Mol were showing maximum binding affinities than the known biomolecular target of NNK 1UGH (Uracil-DNA glycosylase,-7.82Kcal/Mol).

CONCLUSION

CNTs can be applied as chemo-preventive agents against environmental and tobacco induced carcinogens owing to their scavenging potential and warrants for in vivo and in vitro experimental validation of the results obtained from the present study.
.

摘要

目的

DNA损伤是细胞内由内在和外在因素引起的一个持续过程,但它会定期得到修复。如果DNA修复过程出现故障,损伤/突变的发生率就会在细胞中积累,导致细胞转化。据推测,即使在基因、翻译或翻译后阶段的某一点上,DNA修复途径中的负面变化对于致癌作用的起始和发展可能相当关键。因此,在本研究中,我们调查了烟草特异性亚硝胺(TSNs)相关致癌物与DNA修复机制中所涉及酶相互作用的可能性。

方法

香烟烟雾的衍生物如NNK和NNAL是广为人知且公认的致癌物。因此,对在DNA修复过程中起关键作用的近120种酶与NNK和NNAL的反应活性进行了分析。

结果

分子对接研究有助于筛选出NNK的7种可能的DNA修复酶靶点和NNAL的12种靶点。目前的研究揭示了在存在NNK和NNAL的情况下DNA修复酶活性的丧失,这种积累可能诱导DNA损伤的倾向,从而导致暴露的正常细胞转化为癌细胞。本研究还证明了纳米颗粒如单壁碳纳米管/多壁碳纳米管对TSN诱导毒性的保护潜力;在此,单壁碳纳米管对NNK(-17.16千卡/摩尔)和多壁碳纳米管对NNK(-17.01千卡/摩尔)显示出比NNK已知的生物分子靶点1UGH(尿嘧啶-DNA糖基化酶,-7.82千卡/摩尔)更高的结合亲和力。

结论

由于碳纳米管具有清除潜力,可作为针对环境和烟草诱导致癌物的化学预防剂,并且有必要对本研究所得结果进行体内和体外实验验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/442415f818bb/APJCP-21-3099-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/8acd0105f87e/APJCP-21-3099-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/d1d95cfe7bac/APJCP-21-3099-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/088997815e4b/APJCP-21-3099-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/06e67eb95c23/APJCP-21-3099-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/a3d0d0af4a98/APJCP-21-3099-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/72be74c5bd00/APJCP-21-3099-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/456a2d09b854/APJCP-21-3099-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/442415f818bb/APJCP-21-3099-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/8acd0105f87e/APJCP-21-3099-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/d1d95cfe7bac/APJCP-21-3099-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/088997815e4b/APJCP-21-3099-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/06e67eb95c23/APJCP-21-3099-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/a3d0d0af4a98/APJCP-21-3099-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/72be74c5bd00/APJCP-21-3099-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/456a2d09b854/APJCP-21-3099-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeec/7798159/442415f818bb/APJCP-21-3099-g008.jpg

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