Resveratrol for cancer therapy: Challenges and future perspectives

Resveratrol (3,4’,5-trihydroxy-trans-stilbene) has been expected to ameliorate cancer and foster breakthroughs in cancer therapy. Despite thousands of preclinical studies on the anticancer activity of resveratrol, little progress has been made in translational research and clinical trials. Most stud...

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Vydané v:Cancer letters Ročník 515; s. 63 - 72
Hlavní autori: Ren, Boxu, Kwah, Marabeth Xin-Yi, Liu, Cuiliu, Ma, Zhaowu, Shanmugam, Muthu K., Ding, Lingwen, Xiang, Xiaoqiang, Ho, Paul Chi-Lui, Wang, Lingzhi, Ong, Pei Shi, Goh, Boon Cher
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Ireland Elsevier B.V 01.09.2021
Elsevier Limited
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ISSN:0304-3835, 1872-7980, 1872-7980
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Abstract Resveratrol (3,4’,5-trihydroxy-trans-stilbene) has been expected to ameliorate cancer and foster breakthroughs in cancer therapy. Despite thousands of preclinical studies on the anticancer activity of resveratrol, little progress has been made in translational research and clinical trials. Most studies have focused on its anticancer effects, cellular mechanisms, and signal transduction pathways in vitro and in vivo. In this review, we aimed to discern the causes that prevent resveratrol from being used in cancer treatment. Among the various limitations, poor pharmacokinetics and low potency seem to be the two main bottlenecks of resveratrol. In addition, resveratrol-induced nephrotoxicity in multiple myeloma patients hinders its further development as an anticancer drug. New insights and strategies have been proposed to accelerate the conversion of resveratrol from bench to bedside. In the interim, the most promising approach is to enhance the bioavailability of resveratrol with new formulations. Alternatively, more potent analogues of resveratrol could be developed to augment its anticancer potency. Given all the gaps mentioned, much work remains to be done. However, if remarkable progress can be made, resveratrol may finally be used for cancer therapy. •Resveratrol attractive for treatment of colorectal and obesity-related cancers.•Poor bioavailability and low potency compromises anticancer activity of resveratrol.•Unconventional hermetic nature requires further investigation.
AbstractList Resveratrol (3,4',5-trihydroxy-trans-stilbene) has been expected to ameliorate cancer and foster breakthroughs in cancer therapy. Despite thousands of preclinical studies on the anticancer activity of resveratrol, little progress has been made in translational research and clinical trials. Most studies have focused on its anticancer effects, cellular mechanisms, and signal transduction pathways in vitro and in vivo. In this review, we aimed to discern the causes that prevent resveratrol from being used in cancer treatment. Among the various limitations, poor pharmacokinetics and low potency seem to be the two main bottlenecks of resveratrol. In addition, resveratrol-induced nephrotoxicity in multiple myeloma patients hinders its further development as an anticancer drug. New insights and strategies have been proposed to accelerate the conversion of resveratrol from bench to bedside. In the interim, the most promising approach is to enhance the bioavailability of resveratrol with new formulations. Alternatively, more potent analogues of resveratrol could be developed to augment its anticancer potency. Given all the gaps mentioned, much work remains to be done. However, if remarkable progress can be made, resveratrol may finally be used for cancer therapy.Resveratrol (3,4',5-trihydroxy-trans-stilbene) has been expected to ameliorate cancer and foster breakthroughs in cancer therapy. Despite thousands of preclinical studies on the anticancer activity of resveratrol, little progress has been made in translational research and clinical trials. Most studies have focused on its anticancer effects, cellular mechanisms, and signal transduction pathways in vitro and in vivo. In this review, we aimed to discern the causes that prevent resveratrol from being used in cancer treatment. Among the various limitations, poor pharmacokinetics and low potency seem to be the two main bottlenecks of resveratrol. In addition, resveratrol-induced nephrotoxicity in multiple myeloma patients hinders its further development as an anticancer drug. New insights and strategies have been proposed to accelerate the conversion of resveratrol from bench to bedside. In the interim, the most promising approach is to enhance the bioavailability of resveratrol with new formulations. Alternatively, more potent analogues of resveratrol could be developed to augment its anticancer potency. Given all the gaps mentioned, much work remains to be done. However, if remarkable progress can be made, resveratrol may finally be used for cancer therapy.
Resveratrol (3,4’,5-trihydroxy-trans-stilbene) has been expected to ameliorate cancer and foster breakthroughs in cancer therapy. Despite thousands of preclinical studies on the anticancer activity of resveratrol, little progress has been made in translational research and clinical trials. Most studies have focused on its anticancer effects, cellular mechanisms, and signal transduction pathways in vitro and in vivo. In this review, we aimed to discern the causes that prevent resveratrol from being used in cancer treatment. Among the various limitations, poor pharmacokinetics and low potency seem to be the two main bottlenecks of resveratrol. In addition, resveratrol-induced nephrotoxicity in multiple myeloma patients hinders its further development as an anticancer drug. New insights and strategies have been proposed to accelerate the conversion of resveratrol from bench to bedside. In the interim, the most promising approach is to enhance the bioavailability of resveratrol with new formulations. Alternatively, more potent analogues of resveratrol could be developed to augment its anticancer potency. Given all the gaps mentioned, much work remains to be done. However, if remarkable progress can be made, resveratrol may finally be used for cancer therapy.
Resveratrol (3,4’,5-trihydroxy-trans-stilbene) has been expected to ameliorate cancer and foster breakthroughs in cancer therapy. Despite thousands of preclinical studies on the anticancer activity of resveratrol, little progress has been made in translational research and clinical trials. Most studies have focused on its anticancer effects, cellular mechanisms, and signal transduction pathways in vitro and in vivo. In this review, we aimed to discern the causes that prevent resveratrol from being used in cancer treatment. Among the various limitations, poor pharmacokinetics and low potency seem to be the two main bottlenecks of resveratrol. In addition, resveratrol-induced nephrotoxicity in multiple myeloma patients hinders its further development as an anticancer drug. New insights and strategies have been proposed to accelerate the conversion of resveratrol from bench to bedside. In the interim, the most promising approach is to enhance the bioavailability of resveratrol with new formulations. Alternatively, more potent analogues of resveratrol could be developed to augment its anticancer potency. Given all the gaps mentioned, much work remains to be done. However, if remarkable progress can be made, resveratrol may finally be used for cancer therapy. •Resveratrol attractive for treatment of colorectal and obesity-related cancers.•Poor bioavailability and low potency compromises anticancer activity of resveratrol.•Unconventional hermetic nature requires further investigation.
Author Liu, Cuiliu
Ding, Lingwen
Ong, Pei Shi
Kwah, Marabeth Xin-Yi
Xiang, Xiaoqiang
Shanmugam, Muthu K.
Wang, Lingzhi
Ma, Zhaowu
Ho, Paul Chi-Lui
Ren, Boxu
Goh, Boon Cher
Author_xml – sequence: 1
  givenname: Boxu
  surname: Ren
  fullname: Ren, Boxu
  organization: School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China
– sequence: 2
  givenname: Marabeth Xin-Yi
  surname: Kwah
  fullname: Kwah, Marabeth Xin-Yi
  organization: Department of Pharmacy, Faculty of Science, National University of Singapore, Singapore, 117543, Singapore
– sequence: 3
  givenname: Cuiliu
  surname: Liu
  fullname: Liu, Cuiliu
  organization: School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China
– sequence: 4
  givenname: Zhaowu
  surname: Ma
  fullname: Ma, Zhaowu
  organization: School of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China
– sequence: 5
  givenname: Muthu K.
  surname: Shanmugam
  fullname: Shanmugam, Muthu K.
  organization: Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117600, Singapore
– sequence: 6
  givenname: Lingwen
  surname: Ding
  fullname: Ding, Lingwen
  organization: Department of Pathology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117600, Singapore
– sequence: 7
  givenname: Xiaoqiang
  orcidid: 0000-0002-8683-2603
  surname: Xiang
  fullname: Xiang, Xiaoqiang
  organization: Department of Clinical Pharmacy, School of Pharmacy, Fudan University, Shanghai, 201203, China
– sequence: 8
  givenname: Paul Chi-Lui
  surname: Ho
  fullname: Ho, Paul Chi-Lui
  organization: Department of Pharmacy, Faculty of Science, National University of Singapore, Singapore, 117543, Singapore
– sequence: 9
  givenname: Lingzhi
  surname: Wang
  fullname: Wang, Lingzhi
  email: csiwl@nus.edu.sg
  organization: Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117600, Singapore
– sequence: 10
  givenname: Pei Shi
  surname: Ong
  fullname: Ong, Pei Shi
  email: phaops@nus.edu.sg
  organization: Department of Pharmacy, Faculty of Science, National University of Singapore, Singapore, 117543, Singapore
– sequence: 11
  givenname: Boon Cher
  surname: Goh
  fullname: Goh, Boon Cher
  email: phcgbc@nus.edu.sg
  organization: Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117600, Singapore
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34052324$$D View this record in MEDLINE/PubMed
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Fri Feb 23 02:43:27 EST 2024
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IsDoiOpenAccess true
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Keywords Cmax
PGE2
Pharmacodynamics
AST
Cancer treatment
Toxicity
VEGF
ALT
IGF-1
Vd
RASSF-1a
MCP1
IGFBP-3
MPX
TNF-α
Resveratrol
IC50
Tmax
AMPK
Pharmacokinetics
Wnt
Language English
License This is an open access article under the CC BY-NC-ND license.
Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.
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ORCID 0000-0002-8683-2603
OpenAccessLink https://dx.doi.org/10.1016/j.canlet.2021.05.001
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PublicationTitle Cancer letters
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Snippet Resveratrol (3,4’,5-trihydroxy-trans-stilbene) has been expected to ameliorate cancer and foster breakthroughs in cancer therapy. Despite thousands of...
Resveratrol (3,4',5-trihydroxy-trans-stilbene) has been expected to ameliorate cancer and foster breakthroughs in cancer therapy. Despite thousands of...
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StartPage 63
SubjectTerms Animals
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Antitumor activity
Antitumor agents
Bioavailability
Biomarkers
Cancer
Cancer therapies
Cancer treatment
Chemotherapy
Clinical trials
Colorectal cancer
Cytotoxicity
Functional foods & nutraceuticals
Humans
Insulin
Insulin-like growth factors
Multiple myeloma
Neoplasms - drug therapy
Pharmacodynamics
Pharmacokinetics
Plasma
Proteins
Resveratrol
Resveratrol - pharmacology
Resveratrol - therapeutic use
Signal transduction
Signal Transduction - drug effects
Skin
Toxicity
trans-Stilbene
Tumor necrosis factor-TNF
Tumorigenesis
Title Resveratrol for cancer therapy: Challenges and future perspectives
URI https://www.clinicalkey.com/#!/content/1-s2.0-S030438352100197X
https://dx.doi.org/10.1016/j.canlet.2021.05.001
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