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Discovery of Leptulipin, a New Anticancer Protein from theIranian Scorpion, Hemiscorpius lepturus
Cancer is one of the leading causes of mortality in the world. Unfortunately, the present anticancer chemotherapeutics display high cytotoxicity. Accordingly, the discovery of new anticancer agents with lower side effects is highly necessitated. This study aimed to discover an anticancer compound fr...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000277/ https://www.ncbi.nlm.nih.gov/pubmed/35408455 http://dx.doi.org/10.3390/molecules27072056 |
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author | Rezaei, Ali Asgari, Saeme Komijani, Samira Sadat, Seyedeh Narjes Sabatier, Jean-Marc Nasrabadi, Davood Pooshang Bagheri, Kamran Shahbazzadeh, Delavar Akbari Eidgahi, Mohammad Reza De Waard, Michel Mirzahoseini, Hasan |
author_facet | Rezaei, Ali Asgari, Saeme Komijani, Samira Sadat, Seyedeh Narjes Sabatier, Jean-Marc Nasrabadi, Davood Pooshang Bagheri, Kamran Shahbazzadeh, Delavar Akbari Eidgahi, Mohammad Reza De Waard, Michel Mirzahoseini, Hasan |
author_sort | Rezaei, Ali |
collection | PubMed |
description | Cancer is one of the leading causes of mortality in the world. Unfortunately, the present anticancer chemotherapeutics display high cytotoxicity. Accordingly, the discovery of new anticancer agents with lower side effects is highly necessitated. This study aimed to discover an anticancer compound from Hemiscorpius lepturus scorpion venom. Bioactivity-guided chromatography was performed to isolate an active compound against colon and breast cancer cell lines. 2D electrophoresis and MALDI-TOF were performed to identify the molecule. A partial protein sequence was obtained by mass spectrometry, while the full-length was deciphered using a cDNA library of the venom gland by bioinformatics analyses and was designated as leptulipin. The gene was cloned in pET-26b, expressed, and purified. The anticancer effect and mechanism action of leptulipin were evaluated by MTT, apoptosis, and cell cycle assays, as well as by gene expression analysis of apoptosis-related genes. The treated cells displayed inhibition of cell proliferation, altered morphology, DNA fragmentation, and cell cycle arrest. Furthermore, the treated cells showed a decrease in BCL-2 expression and an increase in Bax and Caspase 9 genes. In this study, we discovered a new anticancer protein from H. lepturus scorpion venom. Leptulipin showed significant anticancer activity against breast and colon cancer cell lines. |
format | Online Article Text |
id | pubmed-9000277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90002772022-04-12 Discovery of Leptulipin, a New Anticancer Protein from theIranian Scorpion, Hemiscorpius lepturus Rezaei, Ali Asgari, Saeme Komijani, Samira Sadat, Seyedeh Narjes Sabatier, Jean-Marc Nasrabadi, Davood Pooshang Bagheri, Kamran Shahbazzadeh, Delavar Akbari Eidgahi, Mohammad Reza De Waard, Michel Mirzahoseini, Hasan Molecules Article Cancer is one of the leading causes of mortality in the world. Unfortunately, the present anticancer chemotherapeutics display high cytotoxicity. Accordingly, the discovery of new anticancer agents with lower side effects is highly necessitated. This study aimed to discover an anticancer compound from Hemiscorpius lepturus scorpion venom. Bioactivity-guided chromatography was performed to isolate an active compound against colon and breast cancer cell lines. 2D electrophoresis and MALDI-TOF were performed to identify the molecule. A partial protein sequence was obtained by mass spectrometry, while the full-length was deciphered using a cDNA library of the venom gland by bioinformatics analyses and was designated as leptulipin. The gene was cloned in pET-26b, expressed, and purified. The anticancer effect and mechanism action of leptulipin were evaluated by MTT, apoptosis, and cell cycle assays, as well as by gene expression analysis of apoptosis-related genes. The treated cells displayed inhibition of cell proliferation, altered morphology, DNA fragmentation, and cell cycle arrest. Furthermore, the treated cells showed a decrease in BCL-2 expression and an increase in Bax and Caspase 9 genes. In this study, we discovered a new anticancer protein from H. lepturus scorpion venom. Leptulipin showed significant anticancer activity against breast and colon cancer cell lines. MDPI 2022-03-22 /pmc/articles/PMC9000277/ /pubmed/35408455 http://dx.doi.org/10.3390/molecules27072056 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rezaei, Ali Asgari, Saeme Komijani, Samira Sadat, Seyedeh Narjes Sabatier, Jean-Marc Nasrabadi, Davood Pooshang Bagheri, Kamran Shahbazzadeh, Delavar Akbari Eidgahi, Mohammad Reza De Waard, Michel Mirzahoseini, Hasan Discovery of Leptulipin, a New Anticancer Protein from theIranian Scorpion, Hemiscorpius lepturus |
title | Discovery of Leptulipin, a New Anticancer Protein from theIranian Scorpion, Hemiscorpius lepturus |
title_full | Discovery of Leptulipin, a New Anticancer Protein from theIranian Scorpion, Hemiscorpius lepturus |
title_fullStr | Discovery of Leptulipin, a New Anticancer Protein from theIranian Scorpion, Hemiscorpius lepturus |
title_full_unstemmed | Discovery of Leptulipin, a New Anticancer Protein from theIranian Scorpion, Hemiscorpius lepturus |
title_short | Discovery of Leptulipin, a New Anticancer Protein from theIranian Scorpion, Hemiscorpius lepturus |
title_sort | discovery of leptulipin, a new anticancer protein from theiranian scorpion, hemiscorpius lepturus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9000277/ https://www.ncbi.nlm.nih.gov/pubmed/35408455 http://dx.doi.org/10.3390/molecules27072056 |
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