Evidence map›Paper›PMID 25901198›Full record

ArticleAmerican journal of translational research2015

Molecular docking and inhibition of matrix metalloproteinase-2 by novel difluorinatedbenzylidene curcumin analog.

Aamir Ahmad, Afreen Sayed, Kevin R Ginnebaugh, Vivek Sharma, Anita Suri, Arundhati Saraph, Subhash Padhye, Fazlul H Sarkar

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  8. Article
  9. Review
  10. Article
  11. Article
  12. miR-874: An Important Regulator in Human Diseases.Frontiers in cell and developmental biology · 2022
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. The Role of Curcumin in Prevention and Management of Metastatic Disease.International journal of molecular sciences · 2018
    Review
  18. Article
  19. Review
  20. Review
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

8 authors at 3 institutions in 2 countries.

Aamir AhmadDepartment of Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine Detroit, MI 48201, USA.
Afreen SayedISTRA, Department of Microbiology, Abeda Inamdar Senior College, University of Pune Pune 411001, India.
Kevin R GinnebaughDepartment of Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine Detroit, MI 48201, USA.
Vivek SharmaTata Consultancy Services Hinjewadi, Pune, India.
Anita SuriTata Consultancy Services Hinjewadi, Pune, India.
Arundhati SaraphTata Consultancy Services Hinjewadi, Pune, India.
Subhash PadhyeISTRA, Department of Chemistry, Abeda Inamdar Senior College, University of Pune Pune 411001, India.
Fazlul H SarkarDepartment of Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine Detroit, MI 48201, USA ; Department of Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine Detroit, MI 48201, USA.
Tata Consultancy Services (India) · INThe Barbara Ann Karmanos Cancer Institute · USSavitribai Phule Pune University · IN

Funding

Prevention of Tumor Progression by a Novel ApproachR01CA154321 · NCI · WAYNE STATE UNIVERSITY · PI SARKAR, FAZLUL H. · 2011 to 2015
$1.5M
NCI NIH HHS R01 CA154321
6 · The paper itself

Abstract

We recently described the synthesis and characterization of a novel difluorinatedbenzylidene analog of curcumin, commonly referred as CDF, which demonstrated significantly enhanced bioavailability and in vivo anticancer activity. CDF targets many factors similar to curcumin, albeit with more potency, as reported previously. To further highlight this differential behavior of CDF, we chose matrix metalloproteinase protein MMP-2 which is involved in the processes of invasion and metastasis of human tumors. Both curcumin and CDF were characterized for their binding characteristics using in silico docking studies; they were also evaluated via biological assays involving gelatin zymography, miRNA analysis, invasion assays and ELISA. CDF was found to inhibit MMP-2 expression and activity in A549 and H1299 NSCLC cells much more effectively than curcumin, validating molecular modeling results. miR-874, an MMP-2-targeting miRNA, was up-regulated by CDF. Thus, it appears that CDF can inhibit MMP-2 through multiple mechanisms. Our results are suggestive of a more potent inhibition of invasion and metastasis by CDF, compared to curcumin, thus warranting its further evaluation as an effective anticancer agent.

Indexed as

CDFcurcuminin silico molecular dockingmiR-874MMP-2

Identifiers

PMID25901198
PMCPMC4399093
OpenAlexW300485825

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.