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Lupeol alters viability of SK-RC-45 (Renal cell carcinoma cell line) by modulating its mitochondrial dynamics
Renal cell carcinoma (RCC) is the most common kidney cancer leading to 140,000 deaths per year. Among all RCCs 80% evolve from the epithelial proximal tubular cells within the kidney. There is a high tendency of developing chemoresistance and resistance to radiation therapy in most RCC patients. The...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690575/ https://www.ncbi.nlm.nih.gov/pubmed/31417967 http://dx.doi.org/10.1016/j.heliyon.2019.e02107 |
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author | Sinha, Krishnendu Chowdhury, Sayantani Banerjee, Sharmistha Mandal, Bhagirath Mandal, Mullicka Majhi, Sasadhar Brahmachari, Goutam Ghosh, Jyotirmoy Sil, Parames C. |
author_facet | Sinha, Krishnendu Chowdhury, Sayantani Banerjee, Sharmistha Mandal, Bhagirath Mandal, Mullicka Majhi, Sasadhar Brahmachari, Goutam Ghosh, Jyotirmoy Sil, Parames C. |
author_sort | Sinha, Krishnendu |
collection | PubMed |
description | Renal cell carcinoma (RCC) is the most common kidney cancer leading to 140,000 deaths per year. Among all RCCs 80% evolve from the epithelial proximal tubular cells within the kidney. There is a high tendency of developing chemoresistance and resistance to radiation therapy in most RCC patients. Therefore, kidney resection is considered as the most effective treatments for patients having localized RCC. There is a high tendency of post-operative recurrence among 20–40% of the patients and this recurrence is not curable. It is also clear that modern medicine has no curative treatment options against metastatic RCC. Lupeol [lup-20(29)-en-3β-ol] is a pentacyclic triterpenoid compound naturally found in various edible fruits and in many traditionally used medicinal plants, and has been demonstrated as effective against highly metastatic melanoma and prostate cancers. The present study was designed to evaluate the effect of lupeol to RCC with molecular details. Treatment with lupeol on SK-RC-45 (a RCC cell line) with the LC(50) dose of 40μM (for 48 h) induces mitochondrial hyper fission which eventually leads to apoptosis while SK-RC-45 counteracts by enhancing autophagy-mediated selective removal of fragmented mitochondria. This is the first study which concurrently reports the effects of lupeol on RCC and its effect on the mitochondrial dynamics of a cell. Herein, we conclude that lupeol has potential to be an effective agent against RCC with the modulation of mitochondrial dynamics. |
format | Online Article Text |
id | pubmed-6690575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-66905752019-08-15 Lupeol alters viability of SK-RC-45 (Renal cell carcinoma cell line) by modulating its mitochondrial dynamics Sinha, Krishnendu Chowdhury, Sayantani Banerjee, Sharmistha Mandal, Bhagirath Mandal, Mullicka Majhi, Sasadhar Brahmachari, Goutam Ghosh, Jyotirmoy Sil, Parames C. Heliyon Article Renal cell carcinoma (RCC) is the most common kidney cancer leading to 140,000 deaths per year. Among all RCCs 80% evolve from the epithelial proximal tubular cells within the kidney. There is a high tendency of developing chemoresistance and resistance to radiation therapy in most RCC patients. Therefore, kidney resection is considered as the most effective treatments for patients having localized RCC. There is a high tendency of post-operative recurrence among 20–40% of the patients and this recurrence is not curable. It is also clear that modern medicine has no curative treatment options against metastatic RCC. Lupeol [lup-20(29)-en-3β-ol] is a pentacyclic triterpenoid compound naturally found in various edible fruits and in many traditionally used medicinal plants, and has been demonstrated as effective against highly metastatic melanoma and prostate cancers. The present study was designed to evaluate the effect of lupeol to RCC with molecular details. Treatment with lupeol on SK-RC-45 (a RCC cell line) with the LC(50) dose of 40μM (for 48 h) induces mitochondrial hyper fission which eventually leads to apoptosis while SK-RC-45 counteracts by enhancing autophagy-mediated selective removal of fragmented mitochondria. This is the first study which concurrently reports the effects of lupeol on RCC and its effect on the mitochondrial dynamics of a cell. Herein, we conclude that lupeol has potential to be an effective agent against RCC with the modulation of mitochondrial dynamics. Elsevier 2019-08-02 /pmc/articles/PMC6690575/ /pubmed/31417967 http://dx.doi.org/10.1016/j.heliyon.2019.e02107 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sinha, Krishnendu Chowdhury, Sayantani Banerjee, Sharmistha Mandal, Bhagirath Mandal, Mullicka Majhi, Sasadhar Brahmachari, Goutam Ghosh, Jyotirmoy Sil, Parames C. Lupeol alters viability of SK-RC-45 (Renal cell carcinoma cell line) by modulating its mitochondrial dynamics |
title | Lupeol alters viability of SK-RC-45 (Renal cell carcinoma cell line) by modulating its mitochondrial dynamics |
title_full | Lupeol alters viability of SK-RC-45 (Renal cell carcinoma cell line) by modulating its mitochondrial dynamics |
title_fullStr | Lupeol alters viability of SK-RC-45 (Renal cell carcinoma cell line) by modulating its mitochondrial dynamics |
title_full_unstemmed | Lupeol alters viability of SK-RC-45 (Renal cell carcinoma cell line) by modulating its mitochondrial dynamics |
title_short | Lupeol alters viability of SK-RC-45 (Renal cell carcinoma cell line) by modulating its mitochondrial dynamics |
title_sort | lupeol alters viability of sk-rc-45 (renal cell carcinoma cell line) by modulating its mitochondrial dynamics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690575/ https://www.ncbi.nlm.nih.gov/pubmed/31417967 http://dx.doi.org/10.1016/j.heliyon.2019.e02107 |
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