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Matrine suppresses KRAS‐driven pancreatic cancer growth by inhibiting autophagy‐mediated energy metabolism

Matrine is a natural compound extracted from the herb Sophora flavescens Ait which is widely used in traditional Chinese medicine for treating various diseases. Recently, matrine was reported to have antitumor effects against a variety of cancers without any obvious side effects; however, the molecu...

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Autores principales: Cho, Young‐ra, Lee, Ji Hyeon, Kim, Ji Hye, Lee, So‐Yeon, Yoo, Suna, Jung, Min‐kyo, Kim, Su Jung, Yoo, Hyun Ju, Pack, Chang‐Gi, Rho, Jin Kyung, Son, Jaekyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026868/
https://www.ncbi.nlm.nih.gov/pubmed/29791786
http://dx.doi.org/10.1002/1878-0261.12324
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author Cho, Young‐ra
Lee, Ji Hyeon
Kim, Ji Hye
Lee, So‐Yeon
Yoo, Suna
Jung, Min‐kyo
Kim, Su Jung
Yoo, Hyun Ju
Pack, Chang‐Gi
Rho, Jin Kyung
Son, Jaekyoung
author_facet Cho, Young‐ra
Lee, Ji Hyeon
Kim, Ji Hye
Lee, So‐Yeon
Yoo, Suna
Jung, Min‐kyo
Kim, Su Jung
Yoo, Hyun Ju
Pack, Chang‐Gi
Rho, Jin Kyung
Son, Jaekyoung
author_sort Cho, Young‐ra
collection PubMed
description Matrine is a natural compound extracted from the herb Sophora flavescens Ait which is widely used in traditional Chinese medicine for treating various diseases. Recently, matrine was reported to have antitumor effects against a variety of cancers without any obvious side effects; however, the molecular mechanisms of its antiproliferative effects on cancer are unclear. Here, we report that matrine inhibits autophagy‐mediated energy metabolism, which is necessary for pancreatic cancer growth. We found that matrine significantly reduces pancreatic cancer growth in vitro and in vivo by insufficiently maintaining mitochondrial metabolic function and energy level. We also found that either pyruvate or α‐ketoglutarate supplementation markedly rescues pancreatic cancer cell growth following matrine treatment. Inhibition of mitochondrial energy production results from matrine‐mediated autophagy inhibition by impairing the function of lysosomal protease. Matrine‐mediated autophagy inhibition requires stat3 downregulation. Furthermore, we found that the antitumor effect of matrine on pancreatic cancer growth depends on the mutation of the KRAS oncogene. Together, our data suggest that matrine can suppress the growth of KRAS‐mutant pancreatic cancer by inhibiting autophagy‐mediated energy metabolism.
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spelling pubmed-60268682018-07-09 Matrine suppresses KRAS‐driven pancreatic cancer growth by inhibiting autophagy‐mediated energy metabolism Cho, Young‐ra Lee, Ji Hyeon Kim, Ji Hye Lee, So‐Yeon Yoo, Suna Jung, Min‐kyo Kim, Su Jung Yoo, Hyun Ju Pack, Chang‐Gi Rho, Jin Kyung Son, Jaekyoung Mol Oncol Research Articles Matrine is a natural compound extracted from the herb Sophora flavescens Ait which is widely used in traditional Chinese medicine for treating various diseases. Recently, matrine was reported to have antitumor effects against a variety of cancers without any obvious side effects; however, the molecular mechanisms of its antiproliferative effects on cancer are unclear. Here, we report that matrine inhibits autophagy‐mediated energy metabolism, which is necessary for pancreatic cancer growth. We found that matrine significantly reduces pancreatic cancer growth in vitro and in vivo by insufficiently maintaining mitochondrial metabolic function and energy level. We also found that either pyruvate or α‐ketoglutarate supplementation markedly rescues pancreatic cancer cell growth following matrine treatment. Inhibition of mitochondrial energy production results from matrine‐mediated autophagy inhibition by impairing the function of lysosomal protease. Matrine‐mediated autophagy inhibition requires stat3 downregulation. Furthermore, we found that the antitumor effect of matrine on pancreatic cancer growth depends on the mutation of the KRAS oncogene. Together, our data suggest that matrine can suppress the growth of KRAS‐mutant pancreatic cancer by inhibiting autophagy‐mediated energy metabolism. John Wiley and Sons Inc. 2018-06-11 2018-06 /pmc/articles/PMC6026868/ /pubmed/29791786 http://dx.doi.org/10.1002/1878-0261.12324 Text en © 2018 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Cho, Young‐ra
Lee, Ji Hyeon
Kim, Ji Hye
Lee, So‐Yeon
Yoo, Suna
Jung, Min‐kyo
Kim, Su Jung
Yoo, Hyun Ju
Pack, Chang‐Gi
Rho, Jin Kyung
Son, Jaekyoung
Matrine suppresses KRAS‐driven pancreatic cancer growth by inhibiting autophagy‐mediated energy metabolism
title Matrine suppresses KRAS‐driven pancreatic cancer growth by inhibiting autophagy‐mediated energy metabolism
title_full Matrine suppresses KRAS‐driven pancreatic cancer growth by inhibiting autophagy‐mediated energy metabolism
title_fullStr Matrine suppresses KRAS‐driven pancreatic cancer growth by inhibiting autophagy‐mediated energy metabolism
title_full_unstemmed Matrine suppresses KRAS‐driven pancreatic cancer growth by inhibiting autophagy‐mediated energy metabolism
title_short Matrine suppresses KRAS‐driven pancreatic cancer growth by inhibiting autophagy‐mediated energy metabolism
title_sort matrine suppresses kras‐driven pancreatic cancer growth by inhibiting autophagy‐mediated energy metabolism
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026868/
https://www.ncbi.nlm.nih.gov/pubmed/29791786
http://dx.doi.org/10.1002/1878-0261.12324
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