Evidence map›Paper›PMID 25929337›Full record

ArticleOncotarget2015

Molecular signatures of sanguinarine in human pancreatic cancer cells: A large scale label-free comparative proteomics approach.

Chandra K Singh, Satwinderjeet Kaur, Jasmine George, Minakshi Nihal, Molly C Pellitteri Hahn, Cameron O Scarlett, Nihal Ahmad

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Proteomics in pancreatic cancer.Biomarker research · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Oxidative medicine and cellular longevity · 2019
    Article
  12. Antiangiogenic Effect of Alkaloids.Oxidative medicine and cellular longevity · 2019
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. 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

7 authors at 1 institution in 1 country.

Chandra K SinghDepartment of Dermatology, University of Wisconsin, Madison, WI, USA.
Satwinderjeet KaurDepartment of Dermatology, University of Wisconsin, Madison, WI, USA.
Jasmine GeorgeDepartment of Dermatology, University of Wisconsin, Madison, WI, USA.
Minakshi NihalDepartment of Dermatology, University of Wisconsin, Madison, WI, USA.
Molly C Pellitteri HahnSchool of Pharmacy, University of Wisconsin, Madison, WI, USA.
Cameron O ScarlettSchool of Pharmacy, University of Wisconsin, Madison, WI, USA.
Nihal AhmadDepartment of Dermatology, University of Wisconsin, Madison, WI, USA.
University of Wisconsin–Madison · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AMY TRENTHAM-DIETZ · 1985 to 2026
$142.6M
Role of Polo-Like Kinase-1 in Melanocytic TransformationR01AR059130 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI AHMAD, NIHAL · 2010 to 2019
$3.8M
Acquisition of a High-Field Dual Source FTICR-MS for Pharmaceutical ResearchS10RR029531 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI LI, LINGJUN · 2011 to 2011
$2.1M
Role of SIRT1 in melanocyte biology and melanocyte transformationR01CA176748 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AHMAD, NIHAL · 2013 to 2017
$1.6M
Enhancing Bioavailability of ResveratrolR21CA149560 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AHMAD, NIHAL, BAILEY, HOWARD H. · 2010 to 2011
$496k
Plk1-Numb Cooperation in MelanomagenesisI01BX001008 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI AHMAD, NIHAL · 2013 to 2016
–
BLRD VA I01 BX001008NCI NIH HHS P30 CA014520NCI NIH HHS R01 CA176748NCI NIH HHS R01CA176748NCI NIH HHS R21 CA149560NCI NIH HHS R21CA149560NCRR NIH HHS 1S10RR029531-01NCRR NIH HHS S10 RR029531NIAMS NIH HHS R01 AR059130NIAMS NIH HHS R01AR059130
6 · The paper itself

Abstract

Pancreatic cancer remains one of the most lethal of all human malignancies with its incidence nearly equaling its mortality rate. Therefore, it's crucial to identify newer mechanism-based agents and targets to effectively manage pancreatic cancer. Plant-derived agents/drugs have historically been useful in cancer therapeutics. Sanguinarine is a plant alkaloid with anti-proliferative effects against cancers, including pancreatic cancer. This study was designed to determine the mechanism of sanguinarine's effects in pancreatic cancer with a hope to obtain useful information to improve the therapeutic options for the management of this neoplasm. We employed a quantitative proteomics approach to define the mechanism of sanguinarine's effects in human pancreatic cancer cells. Proteins from control and sanguinarine-treated pancreatic cancer cells were digested with trypsin, run by nano-LC/MS/MS, and identified with the help of Swiss-Prot database. Results from replicate injections were processed with the SIEVE software to identify proteins with differential expression. We identified 37 differentially expressed proteins (from a total of 3107), which are known to be involved in variety of cellular processes. Four of these proteins (IL33, CUL5, GPS1 and DUSP4) appear to occupy regulatory nodes in key pathways. Further validation by qRT-PCR and immunoblot analyses demonstrated that the dual specificity phosphatase-4 (DUSP4) was significantly upregulated by sanguinarine in BxPC-3 and MIA PaCa-2 cells. Sanguinarine treatment also caused down-regulation of HIF1α and PCNA, and increased cleavage of PARP and Caspase-7. Taken together, sanguinarine appears to have pleotropic effects, as it modulates multiple key signaling pathways, supporting the potential usefulness of sanguinarine against pancreatic cancer.

Indexed as

BenzophenanthridinesCell Line, TumorHumansImmunoblottingIsoquinolinesPancreatic NeoplasmsProteomicsBenzophenanthridinesIsoquinolinessanguinarinechemopreventionDUSP4pancreatic cancerquantitative proteomicssanguinarine

Identifiers

PMID25929337
PMCPMC4496359
OpenAlexW1541139244

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.