Evidence map›Paper›PMID 24959376›Full record

ArticleAmerican journal of cancer research2014

Histone/protein deacetylase SIRT1 is an anticancer therapeutic target.

Bor-Jang Hwang, Amrita Madabushi, Jin Jin, Shiou-Yuh S Lin, A-Lien Lu

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  6. Article
  7. SIRT1 induces tumor invasion by targeting epithelial mesenchymal transition-related pathway and is a prognostic marker in triple negative breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Sirtuin inhibitor sirtinol is an intracellular iron chelator.Chemical communications (Cambridge, England) · 2015
    Article
  13. Article
  14. Clinicopathological and prognostic role of SIRT1 in breast cancer patients: a meta-analysis.International journal of clinical and experimental medicine · 2015
    Article
  15. SIRT1 counteracted the activation of STAT3 and NF-κB to repress the gastric cancer growth.International journal of clinical and experimental medicine · 2014
    Article
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 1 institution in 1 country.

Bor-Jang HwangDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine Baltimore, MD 21201, USA.
Amrita MadabushiDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine Baltimore, MD 21201, USA ; Current address: Department of Natural & Physical Sciences, Life Sciences Institute; Baltimore City Community College Baltimore, MD 21201.
Jin JinDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine Baltimore, MD 21201, USA.
Shiou-Yuh S LinDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine Baltimore, MD 21201, USA.
A-Lien LuDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine Baltimore, MD 21201, USA ; University of Maryland Greenebaum Cancer Center Baltimore, MD 21201, USA.
University of Maryland, Baltimore · US

Funding

REPAIR OF OXIDATIVELY DAMAGED GUANINES IN HUMANR01CA078391 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI LU-CHANG, A-LIEN L · 1998 to 2013
$3.4M
Typhoon FLA 9000 Variable Mode Imaging SystemS10OD011969 · OD · UNIVERSITY OF MARYLAND BALTIMORE · PI LU-CHANG, A-LIEN L · 2012 to 2012
$128k
NCI NIH HHS R01 CA078391NIH HHS S10 OD011969
6 · The paper itself

Abstract

SIRT1, a member of the NAD(+)-dependent histone/protein deacetylase family, is involved in chromatin remodeling, DNA repair, and stress response and is a potential drug target. 5-fluorouracil (FU) and the SN1-type DNA methylating agent temozolomide (TMZ) are anticancer agents. In this study, we demonstrate that sirt1 knockout mouse embryonic fibroblast cells are more sensitive to FU and DNA methylating agents than normal cells. Based on these findings, the chemotherapy efficacy of SIRT1 inhibitors in combination with FU or TMZ were tested with human breast cancer cells. We found that treatments combining SIRT1 inhibitors with FU or TMZ show synergistic reduction of cell viability and colony formation of breast cancer cells. Thus, inhibition of SIRT1 activity provides a novel anticancer strategy.

Indexed as

5-fluorouracilBreast cancerdrug resistancemethylating agentsSIRT1 histone deacetylase

Identifiers

PMID24959376
PMCPMC4065402
OpenAlexW59701332

What OpenQuestion holds

Textmetadata
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.