Evidence map›Paper›PMID 15545975›Full record

ArticleBritish journal of cancer2004

Molecular mechanisms of action and prediction of response to oxaliplatin in colorectal cancer cells.

D Arango, A J Wilson, Q Shi, G A Corner, M J Arañes, C Nicholas, M Lesser, J M Mariadason, L H Augenlicht

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed
8.1field-weighted citation impact, top 2% 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

126 citing papers in PubMed, 274 citations in OpenAlex.

  1. Review
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  16. Tetraarsenic Hexoxide Enhanced the Anticancer Effects ofInternational journal of molecular sciences · 2025
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  17. Leveraging chromatin packing domains to target chemoevasion in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  19. "Non-Classical" Platinum Complexes: A Concise Review.International journal of molecular sciences · 2025
    Review
  20. Article

66 more citing papers are in PubMed but not listed here.

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

9 authors at 5 institutions in 2 countries.

D ArangoOncology Department, Albert Einstein Cancer Center, Montefiore Medical Center, 111 East 210th St, Bronx, NY 10467, USA. diego.arango@helsinki.fi
A J Wilson
Q Shi
G A Corner
M J Arañes
C Nicholas
M Lesser
J M Mariadason
L H Augenlicht
Montefiore Medical Center · USAlbert Einstein College of Medicine · USYeshiva University · USNew York Medical College · USNorthwell Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The platinum compound oxaliplatin has been shown to be an effective chemotherapeutic agent for the treatment of colorectal cancer. In this study, we investigate the molecular mechanisms of action of oxaliplatin to identify means of predicting response to this agent. Exposure of colon cancer cells to oxaliplatin resulted in G2/M arrest and apoptosis. Immunofluorescent staining demonstrated that the apoptotic cascade initiated by oxaliplatin is characterised by translocation of Bax to the mitochondria and cytochrome c release into the cytosol. Oxaliplatin treatment resulted in caspase 3 activation and oxaliplatin-induced apoptosis was abrogated by inhibition of caspase activity with z-VAD-fmk, but was independent of Fas/FasL association. Targeted inactivation of Bax or p53 in HCT116 cells resulted in significantly increased resistance to oxaliplatin. However, the mutational status of p53 was unable to predict response to oxaliplatin in a panel of 30 different colorectal cancer cell lines. In contrast, the expression profile of these 30 cell lines, assessed using a 9216-sequence cDNA microarray, successfully predicted the apoptotic response to oxaliplatin. A leave-one-out cross-validation approach was used to demonstrate a significant correlation between experimentally observed and expression profile predicted apoptosis in response to clinically achievable doses of oxaliplatin (R=0.53; P=0.002). In addition, these microarray experiments identified several genes involved in control of apoptosis and DNA damage repair that were significantly correlated with response to oxaliplatin.

Indexed as

Drug Resistance, NeoplasmAntineoplastic AgentsApoptosisbcl-2-Associated X ProteinCaspase 3Caspase InhibitorsCaspasesCell DivisionColorectal NeoplasmsCytochromes cCytosolEnzyme ActivationG2 PhaseGene Expression ProfilingHumansMitochondriaAntineoplastic AgentsBAX protein, humanbcl-2-Associated X ProteinCASP3 protein, humanCaspase 3Caspase InhibitorsCaspasesCytochromes cOrganoplatinum CompoundsOxaliplatinProto-Oncogene Proteins c-bcl-2Tumor Suppressor Protein p53

Identifiers

PMID15545975
PMCPMC2409767
OpenAlexW2146356730

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.