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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Main Authors: Audrey Hébert, Maxime Parisotto, Marie-Camille Rowell, Alexandra Doré, Ana Fernandez Ruiz, Guillaume Lefrançois, Paloma Kalegari, Gerardo Ferbeyre, Andreea R. Schmitzer
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-87993-3
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spelling 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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