Evidence map›Paper›PMID 20414006›Full record

ArticleOncology2010

NF-kB and Bcl-3 activation are prognostic in metastatic colorectal cancer.

Soham D Puvvada, William K Funkhouser, Kevin Greene, Allison Deal, Haitao Chu, Albert S Baldwin, Joel E Tepper, Bert H O'Neil

Open access · bronzeAbstract read
In one paragraph

Article in Oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
3.0field-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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
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  13. Article
  14. Ferroptosis-RelatedPharmacogenomics and personalized medicine · 2022
    Article
  15. Role of Notch, IL-1 and leptin expression in colorectal cancer.Experimental and therapeutic medicine · 2021
    Article
  16. Review
  17. Article
  18. NF-κB and Its Role in Checkpoint Control.International journal of molecular sciences · 2020
    Review
  19. Review
  20. 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

8 authors at 3 institutions in 1 country.

Soham D PuvvadaDepartment of Internal Medicine, Lineberger Comprehensive Cancer Center, Chapel Hill, NC 27599-7305, USA.
William K Funkhouser
Kevin Greene
Allison Deal
Haitao Chu
Albert S Baldwin
Joel E Tepper
Bert H O'Neil
Cancer Research And Biostatistics · USRadiation Oncology Associates · USUNC Lineberger Comprehensive Cancer Center

Funding

TISSUE PROCUREMENT &ANALYSISP50CA106991 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TEPPER, JOEL E · 2004 to 2009
$12.1M
Radiation-induced signaling and treatment resistanceK23CA118431 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI O'NEIL, BERT HOWARD · 2006 to 2010
$684k
NCI NIH HHS 5K23 CA118431-04NCI NIH HHS 5P50 CA106991-06NCI NIH HHS K23 CA118431NCI NIH HHS P50 CA106991
6 · The paper itself

Abstract

purposeNF-kappaB is an antiapoptotic transcription factor that has been shown to be a mediator of treatment resistance. Bcl-3 is a regulator of NF-kappaB that may play a role in oncogenesis. The goal of this study was to correlate the activation status of NF-kappaB and Bcl-3 with clinical outcome in a group of patients with metastatic colorectal cancer (CRC).

methodsA retrospective study of 23 patients who underwent surgical resection of CRC at the University of North Carolina (UNC). Activation of NF-kappaB was defined by nuclear expression of select components of NF-kappaB (p50, p52, p65) and Bcl-3. Tissue microarrays were created from cores of normal mucosa, primary tumor, lymph node metastases and liver metastases in triplicate from disparate areas of the blocks, and an intensity score was generated by multiplying intensity (0-3+) by percent of positive tumor cells. Generalized estimating equations were used to note differences in intensity scores among normal mucosa and nonnormal tissues. Cox regression models were fit to see if scores were significantly associated with overall survival.

resultsp65 NE was significantly higher in primary tumor and liver metastases than normal mucosa (both p < 0.01). p50 nuclear expression was significantly higher for all tumor sites than for normal mucosa (primary tumor and lymph node metastases p < 0.0001, liver metastases p < 0.01). Bcl-3 nuclear expression did not differ significantly between normal mucosa and tumor; however, nuclear expression in primary tumor for each of these components was strongly associated with survival: the increase in hazard for each 50-point increase in nuclear expression was 91% for Bcl-3, 66% for p65, and 52% for p50 (all p < 0.05).

conclusionsActivation of canonical NF-kappaB subunits p50 and p65 as measured by nuclear expression is strongly associated with survival suggesting NF-kappaB as a prognostic factor in this disease. Primary tumor nuclear expression appears to be as good as, or better than, metastatic sites at predicting prognosis. Bcl-3 nuclear expression is also negatively associated with survival and deserves further study in CRC.

Indexed as

Gene Expression Regulation, NeoplasticAgedB-Cell Lymphoma 3 ProteinCell NucleusColorectal NeoplasmsFemaleHumansImmunohistochemistryLymphatic MetastasisMaleMiddle AgedModels, BiologicalNeoplasm MetastasisNF-kappa BOligonucleotide Array Sequence AnalysisPrognosisB-Cell Lymphoma 3 ProteinBCL3 protein, humanNF-kappa BProto-Oncogene ProteinsTranscription Factors

Identifiers

PMID20414006
PMCPMC2914399
OpenAlexW2019864071

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.