Phenylethynylbenzyl-modified biguanides inhibit pancreatic cancer tumor growth
Abstract We present the design and synthesis of a small library of substituted biguanidium salts and their capacity to inhibit the growth of pancreatic cancer cells. We first present their in vitro and membrane activity, before we address their mechanism of action in living cells and in vivo activit...
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2021-05-01
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Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-021-87993-3 |
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doaj-6a200413183b471cb0be937679e2ef462021-05-11T14:57:44ZengNature Publishing GroupScientific Reports2045-23222021-05-0111111110.1038/s41598-021-87993-3Phenylethynylbenzyl-modified biguanides inhibit pancreatic cancer tumor growthAudrey Hébert0Maxime Parisotto1Marie-Camille Rowell2Alexandra Doré3Ana Fernandez Ruiz4Guillaume Lefrançois5Paloma Kalegari6Gerardo Ferbeyre7Andreea R. Schmitzer8Département de Chimie-Faculté des Arts et des Sciences, Université de MontréalDépartement de Chimie-Faculté des Arts et des Sciences, Université de MontréalDépartement de Biochimie et Médecine Moléculaire, and CRCHUM-Faculté de Médecine, Université de MontréalDépartement de Chimie-Faculté des Arts et des Sciences, Université de MontréalDépartement de Biochimie et Médecine Moléculaire, and CRCHUM-Faculté de Médecine, Université de MontréalDépartement de Chimie-Faculté des Arts et des Sciences, Université de MontréalDépartement de Biochimie et Médecine Moléculaire, and CRCHUM-Faculté de Médecine, Université de MontréalDépartement de Biochimie et Médecine Moléculaire, and CRCHUM-Faculté de Médecine, Université de MontréalDépartement de Chimie-Faculté des Arts et des Sciences, Université de MontréalAbstract We present the design and synthesis of a small library of substituted biguanidium salts and their capacity to inhibit the growth of pancreatic cancer cells. We first present their in vitro and membrane activity, before we address their mechanism of action in living cells and in vivo activity. We show that phenylethynyl biguanidium salts possess higher ability to cross hydrophobic barriers, improve mitochondrial accumulation and anticancer activity. Mechanistically, the most active compound, 1b, like metformin, activated AMPK, decreased the NAD+/NADH ratio and mitochondrial respiration, but at 800-fold lower concentration. In vivo studies show that compound 1b significantly inhibits the growth of pancreatic cancer xenografts in mice, while biguanides currently in clinical trials had little activity.https://doi.org/10.1038/s41598-021-87993-3 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Audrey Hébert Maxime Parisotto Marie-Camille Rowell Alexandra Doré Ana Fernandez Ruiz Guillaume Lefrançois Paloma Kalegari Gerardo Ferbeyre Andreea R. Schmitzer |
spellingShingle |
Audrey Hébert Maxime Parisotto Marie-Camille Rowell Alexandra Doré Ana Fernandez Ruiz Guillaume Lefrançois Paloma Kalegari Gerardo Ferbeyre Andreea R. Schmitzer Phenylethynylbenzyl-modified biguanides inhibit pancreatic cancer tumor growth Scientific Reports |
author_facet |
Audrey Hébert Maxime Parisotto Marie-Camille Rowell Alexandra Doré Ana Fernandez Ruiz Guillaume Lefrançois Paloma Kalegari Gerardo Ferbeyre Andreea R. Schmitzer |
author_sort |
Audrey Hébert |
title |
Phenylethynylbenzyl-modified biguanides inhibit pancreatic cancer tumor growth |
title_short |
Phenylethynylbenzyl-modified biguanides inhibit pancreatic cancer tumor growth |
title_full |
Phenylethynylbenzyl-modified biguanides inhibit pancreatic cancer tumor growth |
title_fullStr |
Phenylethynylbenzyl-modified biguanides inhibit pancreatic cancer tumor growth |
title_full_unstemmed |
Phenylethynylbenzyl-modified biguanides inhibit pancreatic cancer tumor growth |
title_sort |
phenylethynylbenzyl-modified biguanides inhibit pancreatic cancer tumor growth |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-05-01 |
description |
Abstract We present the design and synthesis of a small library of substituted biguanidium salts and their capacity to inhibit the growth of pancreatic cancer cells. We first present their in vitro and membrane activity, before we address their mechanism of action in living cells and in vivo activity. We show that phenylethynyl biguanidium salts possess higher ability to cross hydrophobic barriers, improve mitochondrial accumulation and anticancer activity. Mechanistically, the most active compound, 1b, like metformin, activated AMPK, decreased the NAD+/NADH ratio and mitochondrial respiration, but at 800-fold lower concentration. In vivo studies show that compound 1b significantly inhibits the growth of pancreatic cancer xenografts in mice, while biguanides currently in clinical trials had little activity. |
url |
https://doi.org/10.1038/s41598-021-87993-3 |
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