Evidence map›Paper›PMID 19034969›Full record

ArticleWorld journal of gastroenterology2008

Gene expression profiling: canonical molecular changes and clinicopathological features in sporadic colorectal cancers.

Jin-Cheon Kim, Seon-Young Kim, Seon-Ae Roh, Dong-Hyung Cho, Dae-Dong Kim, Jeong-Hyun Kim, Yong-Sung Kim

Abstract read
In one paragraph

Article in World journal of gastroenterology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. The Emerging Role of Adhesion GPCRs in Cancer.ACS pharmacology & translational science · 2020
    Review
  7. Review
  8. Article
  9. Mitochondrial ribosomes in cancer.Seminars in cancer biology · 2017
    Review
  10. Expression of NIBP and its clinical significance in human early colorectal cancer.International journal of clinical and experimental pathology · 2017
    Article
  11. Article
  12. NIK- and IKKβ-binding protein promotes colon cancer metastasis by activating the classical NF-κB pathway and MMPs.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  13. Adhesion GPCRs in Tumorigenesis.Handbook of experimental pharmacology · 2016
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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.

Jin-Cheon KimDepartment of Surgery, University of Ulsan College of Medicine and Asan Medical Center, 388-1 Poongnap-2-Dong Songpa-Ku, Seoul 138-736, South Korea. jckim@amc.seoul.kr
Seon-Young Kim
Seon-Ae Roh
Dong-Hyung Cho
Dae-Dong Kim
Jeong-Hyun Kim
Yong-Sung Kim

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate alternative or subordinate pathways involved in colorectal tumorigenesis and tumor growth, possibly determining at-risk populations and predicting responses to treatment.

methodsUsing microarray gene-expression analysis, we analyzed patterns of gene expression relative to canonical molecular changes and clinicopathological features in 84 sporadic colorectal cancer patients, standardized by tumor location. Subsets of differentially expressed genes were confirmed by real-time reverse-transcript polymerase chain reaction (RT-PCR).

resultsThe largest number of genes identified as being differentially expressed was by tumor location, and the next largest number by lymphovascular or neural invasion of tumor cells and by mismatch repair (MMR) defects. Amongst biological processes, the immune response was significantly implicated in entire molecular changes observed during colorectal tumorigenesis (P < 0.001). Amongst 47 differentially expressed genes, seven (PISD, NIBP, BAI2, STOML1, MRPL21, MRPL16, and MKKS) were newly found to correlate with tumorigenesis and tumor growth. Most location-associated molecular changes had distinct effects on gene expression, but the effects of the latter were sometimes contradictory.

conclusionWe show that several differentially expressed genes were associated with canonical molecular changes in sporadic colorectal cancers, possibly constituting alternative or subordinate pathways of tumorigenesis. As tumor location was the dominant factor influencing differential gene expression, location-specific analysis may identify location-associated pathways and enhance the accuracy of class prediction.

Indexed as

Cell ProliferationGene Expression ProfilingColorectal NeoplasmsGene Expression Regulation, NeoplasticGenes, APCGenes, p53Genetic Predisposition to DiseaseHumansMutationOligonucleotide Array Sequence AnalysisProspective StudiesRetrospective StudiesSignal TransductionWnt ProteinsWnt Proteins

Identifiers

PMID19034969
PMCPMC2773308

What OpenQuestion holds

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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.