Evidence map›Paper›PMID 31032145›Full record

ArticleJournal of cell science & therapy2018

Proteomics Profiling of Pancreatic Cancer and Pancreatitis for Biomarkers Discovery.

N Sanh, H Fadul, N Hussein, B D Lyn-Cook, G Hammons, X E Ramos-Cardona, K Mohamed, S I Mohammed

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Engineering of biomaterials for tumor modeling.Materials today. Advances · 2020
    Article
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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 4 institutions in 1 country.

N SanhDepartment of Comparative Pathobiology and Purdue University Center for Cancer Research, Purdue University, West Lafayette, USA.
H FadulDepartment of Comparative Pathobiology and Purdue University Center for Cancer Research, Purdue University, West Lafayette, USA.
N HusseinFranklin College, IUPUI- Indiana University Purdue University Indianapolis, Indianapolis, USA.
B D Lyn-CookDivision of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, USA.
G HammonsDivision of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, USA.
X E Ramos-CardonaDepartment of Comparative Pathobiology and Purdue University Center for Cancer Research, Purdue University, West Lafayette, USA.
K MohamedRadiation and Isotopes Center Khartoum (RICK), Sudan.
S I MohammedDepartment of Comparative Pathobiology and Purdue University Center for Cancer Research, Purdue University, West Lafayette, USA.
Purdue University West Lafayette · USNational Center for Toxicological Research · USIndiana University – Purdue University Indianapolis · USInternational Isotopes (United States) · US

Funding

LCM & 2D PAGE in Early Detection of Pancreatic CancerR03CA119310 · NCI · PURDUE UNIVERSITY · PI MOHAMMED, SULMA IBRAHIM · 2006 to 2007
$156k
NCI NIH HHS R03 CA119310
6 · The paper itself

Abstract

Pancreatic cancer is one of the most aggressive malignancies with an increase in incidence predicted, particularly in African Americans. Pancreatic cancer is considered a silent disease with poor prognosis and a lack of early biomarkers for detection. Proteomics has been applied in many diseases for identifying or discovering biomarkers. It has long been suggested that chronic pancreatitis may be a risk factor for developing pancreatic cancer. This study identified proteins that are altered in expression in pancreatic cancer and pancreatitis compared to normal using proteomic technology. Proteins were extracted from laser captured micro-dissected tissues and separated in 2-DPAGE and imaged. The protein profiles of pancreatic cancer and pancreatitis are similar but differed with the protein profile of normal adjacent tissues. Representative proteins, overexpressed in tumor and pancreatitis but not normal tissues, were excised from gels, subjected to in-gel digestion, and analyzed by MALDI-TOF mass spectrometry. Proteins identified included transferrin, ER-60 protein, proapolipoprotein, tropomyosin 1, alpha 1 actin precursor, ACTB protein, and gamma 2 propeptide, aldehyde dehydrogenase 1A1, pancreatic lipase and annexin A1. Several proteins, which were shown in pancreatic cancer, were also observed in pancreatitis samples. Understanding the role of these specific proteins and their mechanistic action will give insights into their involvement in pancreatic cancers.

Indexed as

2D-gelBiomarkersLipasePancreatic cancerPancreatitisProteomic

Identifiers

PMID31032145
PMCPMC6481958
OpenAlexW2916058973

What OpenQuestion holds

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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.