Synthetic oleanane triterpenoid derivative CDDO‐Me disrupts cellular bioenergetics to suppress pancreatic ductal adenocarcinoma via targeting SLC1A5-Reference-Cited by-同舟云学术

Synthetic oleanane triterpenoid derivative CDDO‐Me disrupts cellular bioenergetics to suppress pancreatic ductal adenocarcinoma via targeting SLC1A5

Published:2022-08-05 Issue:11 Volume:36 Page:
ISSN:1095-6670
Container-title:Journal of Biochemical and Molecular Toxicology
language:en
Short-container-title:J Biochem & Molecular Tox

Author:

Akuetteh Percy D. P.¹,Huang Huimin²,Wu Shijia¹,Zhou Hongfei¹,Jin Guihua¹,Hong Welong¹,Yang Hongbao¹,Lan Linhua¹^ORCID,Shangguan Fugen¹,Zhang Qiyu¹³

Affiliation:

1. Key Laboratory of Diagnosis and Treatment of Severe Hepato‐Pancreatic Diseases of Zhejiang Province The First Affiliated Hospital of Wenzhou Medical University Wenzhou China

2. School of Laboratory Medicine and Life Sciences Wenzhou Medical University Wenzhou China

3. Department of Hepatobiliary Surgery The First Affiliated Hospital of Wenzhou Medical University Wenzhou China

Funder

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Toxicology,Molecular Biology,Molecular Medicine,Biochemistry,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jbt.23192

Reference31 articles.

1. Optimizing the outcomes of pancreatic cancer surgery

2. Synthesis and Anticancer Activity of CDDO and CDDO-Me, Two Derivatives of Natural Triterpenoids

3. The Keap1-Nrf2-ARE Pathway As a Potential Preventive and Therapeutic Target: An Update

4. CDDO-Me inhibits tumor growth and prevents recurrence of pancreatic ductal adenocarcinoma

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