Evidence map›Paper›PMID 23401724›Full record

ArticleComputational and mathematical methods in medicine2013

Molecular signature of cancer at gene level or pathway level? Case studies of colorectal cancer and prostate cancer microarray data.

Jiajia Chen, Ying Wang, Bairong Shen, Daqing Zhang

Abstract read
In one paragraph

Article in Computational and mathematical methods in medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

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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, 1 synthesis or guideline pooled it.

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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

4 authors.

Jiajia ChenCenter for Systems Biology, Soochow University, Jiangsu, Suzhou 215006, China.
Ying Wang
Bairong Shen
Daqing Zhang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With recent advances in microarray technology, there has been a flourish in genome-scale identification of molecular signatures for cancer. However, the differentially expressed genes obtained by different laboratories are highly divergent. The present discrepancy at gene level indicates a need for a novel strategy to obtain more robust signatures for cancer. In this paper we hypothesize that (1) the expression signatures of different cancer microarray datasets are more similar at pathway level than at gene level; (2) the comparability of the cancer molecular mechanisms of different individuals is related to their genetic similarities. In support of the hypotheses, we summarized theoretical and experimental evidences, and conducted case studies on colorectal and prostate cancer microarray datasets. Based on the above assumption, we propose that reliable cancer signatures should be investigated in the context of biological pathways, within a cohort of genetically homogeneous population. It is hoped that the hypotheses can guide future research in cancer mechanism and signature discovery.

Indexed as

Data Interpretation, StatisticalAlgorithmsCohort StudiesColorectal NeoplasmsComputational BiologyDNA, ComplementaryGene Expression ProfilingHumansMaleModels, BiologicalModels, GeneticModels, StatisticalOligonucleotide Array Sequence AnalysisProstatic NeoplasmsDNA, Complementary

Identifiers

PMID23401724
PMCPMC3562646

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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.