Evidence map›Paper›PMID 19882219›Full record

ArticleClinical & experimental metastasis2010

Gene expression profiling of primary and metastatic colon cancers identifies a reduced proliferative rate in metastatic tumors.

Ganepola A P Ganepola, Robert M Mazziotta, Dilendra Weeresinghe, Georgia A Corner, Cheryl J Parish, David H Chang, Niall C Tebbutt, Carmel Murone, Naseem Ahmed, Leonard H Augenlicht and 1 more

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Article in Clinical & experimental metastasis, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  7. Gene expression differences in primary colorectal tumors and matched liver metastases: chemotherapy related or tumoral heterogeneity?Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2015
    Article
  8. Review
  9. Biological resonance for cancer metastasis, a new hypothesis based on comparisons between primary cancers and metastases.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2013
    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

11 authors at 6 institutions in 2 countries.

Ganepola A P GanepolaCenter for Cancer Research and Genomic Medicine, The Valley Hospital, Ridgewood, NJ 07450, USA. Ganepola@verizon.net
Robert M Mazziotta
Dilendra Weeresinghe
Georgia A Corner
Cheryl J Parish
David H Chang
Niall C Tebbutt
Carmel Murone
Naseem Ahmed
Leonard H Augenlicht
John M Mariadason
Center for Cancer Research · USMontefiore Medical Center · USLudwig Cancer Research · AUAlbert Einstein College of Medicine · USValley Hospital · USValley Hospital Medical Center · US

Funding

HDAC3 in COLON CANCERR01CA123316 · NCI · MONTEFIORE MEDICAL CENTER (BRONX, NY) · PI MARIADASON, JOHN M · 2007 to 2011
$1.2M
NCI NIH HHS CA123316
6 · The paper itself

Abstract

The objective of this study was to gain insights into the biological basis of the metastatic process by characterizing the gene expression differences between primary and metastatic colon cancers. Recent studies have demonstrated that few new mutational changes are acquired during the metastatic progression of colon tumors [Jones et al., Proc Natl Acad Sci USA 105 (11): 4283-4288, 2008]. However, the extent to which epigenetic and transcriptional changes occur between primary and metastatic colon cancer remains unknown. We approached these issues using Affymetrix microarrays to assess the similarities and differences in gene expression profiles between macro-dissected primary and metastatic colon tumors. Unexpectedly, we found that expression of a number of cell proliferation markers were reduced in the liver metastases of colon tumors when compared to primary tumors. This finding was validated by immunohistochemical staining of Ki67 and Cyclin D1 in Formalin-Fixed Paraffin-Embedded (FFPE) section of the same samples, and in an independent cohort of FFPE matched tumor and metastatic tissue samples. These results indicate that significant transcriptional differences exist between primary and metastatic colon tumors, and demonstrate that metastatic lesions have a lower proliferative rate compared to primary tumors. These findings may have implications for interpreting differences in response rates between primary and metastatic lesions and suggest that measurement of expression-based biomarkers in metastatic tissue will be most informative for understanding the basis of response of metastatic tumors to therapeutic intervention.

Indexed as

Cell ProliferationCell CycleColonic NeoplasmsGene Expression ProfilingHumansNeoplasm MetastasisTissue Array Analysis

Identifiers

PMID19882219
OpenAlexW1972988805

What OpenQuestion holds

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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.