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Design of PD-L1 inhibitors for lung cancer

The progression of lung cancer is associated with inactivation of programmed cell death protein 1, abbreviated as PD- 1 which regulates the suppression of the body's immune system by suppressing T- cell inflammatory activity and is responsible for preventing cancer cell growth. It is of interes...

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Autores principales: Udhwani, Trishang, Mukherjee, Sourav, Sharma, Khushboo, Sweta, Jajoriya, Khandekar, Natasha, Nayarisseri, Anuraj, Singh, Sanjeev Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6677907/
https://www.ncbi.nlm.nih.gov/pubmed/31435160
http://dx.doi.org/10.6026/97320630015139
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author Udhwani, Trishang
Mukherjee, Sourav
Sharma, Khushboo
Sweta, Jajoriya
Khandekar, Natasha
Nayarisseri, Anuraj
Singh, Sanjeev Kumar
author_facet Udhwani, Trishang
Mukherjee, Sourav
Sharma, Khushboo
Sweta, Jajoriya
Khandekar, Natasha
Nayarisseri, Anuraj
Singh, Sanjeev Kumar
author_sort Udhwani, Trishang
collection PubMed
description The progression of lung cancer is associated with inactivation of programmed cell death protein 1, abbreviated as PD- 1 which regulates the suppression of the body's immune system by suppressing T- cell inflammatory activity and is responsible for preventing cancer cell growth. It is of interest to identify inhibitors for PD-L1 dimeric structure through molecular docking and virtual screening. The virtual screened compound XGIQBUNWFCCMAS-UHFFFAOYSA-N (PubChem CID: 127263272) displays a high affinity with the target protein. ADMET analysis and cytotoxicity studies further add weight to this compound as a potential inhibitor of PD-L1. The established compound BMS-202 still shows the high re-rank score, but the virtual screened drug possesses a better ADMET profile with a higher intestinal absorption value and lower toxicity.
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spelling pubmed-66779072019-08-21 Design of PD-L1 inhibitors for lung cancer Udhwani, Trishang Mukherjee, Sourav Sharma, Khushboo Sweta, Jajoriya Khandekar, Natasha Nayarisseri, Anuraj Singh, Sanjeev Kumar Bioinformation Research Article The progression of lung cancer is associated with inactivation of programmed cell death protein 1, abbreviated as PD- 1 which regulates the suppression of the body's immune system by suppressing T- cell inflammatory activity and is responsible for preventing cancer cell growth. It is of interest to identify inhibitors for PD-L1 dimeric structure through molecular docking and virtual screening. The virtual screened compound XGIQBUNWFCCMAS-UHFFFAOYSA-N (PubChem CID: 127263272) displays a high affinity with the target protein. ADMET analysis and cytotoxicity studies further add weight to this compound as a potential inhibitor of PD-L1. The established compound BMS-202 still shows the high re-rank score, but the virtual screened drug possesses a better ADMET profile with a higher intestinal absorption value and lower toxicity. Biomedical Informatics 2019-02-28 /pmc/articles/PMC6677907/ /pubmed/31435160 http://dx.doi.org/10.6026/97320630015139 Text en © 2019 Biomedical Informatics http://creativecommons.org/licenses/by/3.0/ This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License.
spellingShingle Research Article
Udhwani, Trishang
Mukherjee, Sourav
Sharma, Khushboo
Sweta, Jajoriya
Khandekar, Natasha
Nayarisseri, Anuraj
Singh, Sanjeev Kumar
Design of PD-L1 inhibitors for lung cancer
title Design of PD-L1 inhibitors for lung cancer
title_full Design of PD-L1 inhibitors for lung cancer
title_fullStr Design of PD-L1 inhibitors for lung cancer
title_full_unstemmed Design of PD-L1 inhibitors for lung cancer
title_short Design of PD-L1 inhibitors for lung cancer
title_sort design of pd-l1 inhibitors for lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6677907/
https://www.ncbi.nlm.nih.gov/pubmed/31435160
http://dx.doi.org/10.6026/97320630015139
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