Evidence map›Paper›PMID 26959057›Full record

ArticleNutrients2016

Sirt1 Is Required for Resveratrol-Mediated Chemopreventive Effects in Colorectal Cancer Cells.

Constanze Buhrmann, Parviz Shayan, Bastian Popper, Ajay Goel, Mehdi Shakibaei

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed, 2 pooled it
8.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

71 citing papers in PubMed, 2 syntheses or guidelines pooled it, 115 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. The role of NADFrontiers in oncology · 2026
    Review
  7. Review
  8. Review
  9. Exploring the Role ofJournal of clinical medicine · 2025
    Article
  10. Review
  11. Review
  12. The role of SIRT1 in the development of gastrointestinal tumors.Frontiers in cell and developmental biology · 2025
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review

11 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 3 countries.

Constanze BuhrmannInstitute of Anatomy, Ludwig-Maximilian-University Munich, Pettenkoferstrasse 11, Munich D-80336, Germany. constanze.buhrmann@med.uni-muenchen.de.
Parviz ShayanDepartment of Parasitology, Faculty of Veterinary Medicine, University of Tehran, Tehran 141556453, Iran. pshayan@ut.ac.ir.
Bastian PopperDepartment of Anatomy and Cell Biology, Biomedical Center, Ludwig-Maximilian-University Munich, Martinsried D-82152, Germany. Bastian.Popper@med.uni-muenchen.de.
Ajay GoelCenter for Gastrointestinal Research; Center for Epigenetics, Cancer Prevention and Cancer Genomics, Baylor Research Institute and Sammons Cancer Center, Baylor University Medical Center, Dallas, TX 75246, USA. AjayG@BaylorHealth.edu.
Mehdi ShakibaeiInstitute of Anatomy, Ludwig-Maximilian-University Munich, Pettenkoferstrasse 11, Munich D-80336, Germany. mehdi.shakibaei@med.uni-muenchen.de.
Ludwig-Maximilians-Universität München · DEBaylor University Medical Center · USUniversity of Tehran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sirt1 is a NAD⁺-dependent protein-modifying enzyme involved in regulating gene expression, DNA damage repair, metabolism and survival, as well as acts as an important subcellular target of resveratrol. The complex mechanisms underlying Sirt1 signaling during carcinogenesis remain controversial, as it can serve both as a tumor promoter and suppressor. Whether resveratrol-mediated chemopreventive effects are mediated via Sirt1 in CRC growth and metastasis remains unclear; which was the subject of this study. We found that resveratrol suppressed proliferation and invasion of two different human CRC cells in a dose-dependent manner, and interestingly, this was accompanied with a significant decrease in Ki-67 expression. By transient transfection of CRC cells with Sirt1-ASO, we demonstrated that the anti-tumor effects of resveratrol on cells was abolished, suggesting the essential role of this enzyme in the resveratrol signaling pathway. Moreover, resveratrol downregulated nuclear localization of NF-κB, NF-κB phosphorylation and its acetylation, causing attenuation of NF-κB-regulated gene products (MMP-9, CXCR4) involved in tumor-invasion and metastasis. Finally, Sirt1 was found to interact directly with NF-κB, and resveratrol did not suppress Sirt1-ASO-induced NF-κB phosphorylation, acetylation and NF-κB-regulated gene products. Overall, our results demonstrate that resveratrol can suppress tumorigenesis, at least in part by targeting Sirt1 and suppression of NF-κB activation.

Indexed as

AcetylationAntineoplastic AgentsCell MovementCell ProliferationColorectal NeoplasmsDose-Response Relationship, DrugHCT116 CellsHumansKi-67 AntigenMatrix Metalloproteinase 9Neoplasm InvasivenessOligonucleotides, AntisensePhosphorylationReceptors, CXCR4ResveratrolSignal TransductionAntineoplastic AgentsCXCR4 protein, humanKi-67 AntigenMatrix Metalloproteinase 9MMP9 protein, humanOligonucleotides, AntisenseReceptors, CXCR4RELA protein, humanResveratrolSIRT1 protein, humanSirtuin 1StilbenesTranscription Factor RelAalginatecarcinogenesishuman colon cancerNF-κBresveratrolSirt1

Identifiers

PMID26959057
PMCPMC4808874
OpenAlexW2291725186

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.