Evidence map›Paper›PMID 24106912›Full record

ArticleBMC clinical pathology2013

The role and prognostic value of apoptosis in colorectal carcinoma.

Julia Alcaide, Rafael Funez, Antonio Rueda, Elisabeth Perez-Ruiz, Teresa Pereda, Isabel Rodrigo, Rafael Coveñas, Miguel Muñoz, Maximino Redondo

2 registry-linked trialsAbstract read
In one paragraph

Article in BMC clinical pathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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.

NCT05631041 phase3unknown statusnot on this mapstarted 2022, after this paper: background citation

The Possible Anticancer Effect of Silymarin in Patients With Metastatic Colorectal Cancer Receiving Chemotherapy.

TypeinterventionalSponsorTanta UniversityRan2022 to 2024Enrolled64ConditionsMetastatic Colorectal CancerArmsSilymarin
NCT06115174 phase4unknown statusnot on this mapstarted 2023, after this paper: background citation

Clinical Study Evaluating the Anticancer Effect of Pentoxiphylline in Patients With Metastatic Colorectal Cancer

TypeinterventionalSponsorTanta UniversityRan2023 to 2024Enrolled44ConditionsMetastatic Colorectal CarcinomaArmsPentoxifylline, FOLFOX, XELOX, Monoclonal antibodies (target therapy)
3 · Its place in the literature

Who cites it

31 citing papers in PubMed.

  1. Trial
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  8. Knocking down of Xkr8 enhances chemotherapy efficacy through modulating tumor immune microenvironment.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Article
  9. Review
  10. Review
  11. Targeting Angiogenesis via Resolution of Inflammation.Cold Spring Harbor perspectives in medicine · 2023
    Review
  12. Article
  13. Review
  14. Review
  15. The Apoptosis Paradox in Cancer.International journal of molecular sciences · 2022
    Review
  16. Eicosanoid regulation of debris-stimulated metastasis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  17. Debris-stimulated tumor growth: a Pandora's box?Cancer metastasis reviews · 2021
    Review
  18. Review
  19. Review
  20. Review
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.

Julia AlcaideRed de Investigacion en Servicios de Salud (REDISSEC), Spain. mredondo@hcs.es.
Rafael Funez
Antonio Rueda
Elisabeth Perez-Ruiz
Teresa Pereda
Isabel Rodrigo
Rafael Coveñas
Miguel Muñoz
Maximino Redondo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlterations to apoptosis are a common occurrence in human tumours. The aim of our study was to determine the influence of apoptotic variations on the carcinogenesis and prognosis of colorectal carcinomas (CRCs).

methodsA TUNEL assay was performed on archival material from 103 colorectal carcinomas, 26 adenomas and 20 samples of normal epithelia.

resultsThe number of apoptotic cells was higher in CRCs (1.09 ± 0.13) than in adenomas (0.38 ± 0.23, p = 0.059) and normal epithelium (0.06 ± 0.04, p = 0.001). In addition, the apoptotic index (AI) was greater in metastatic disease (stage IV) than in other stages (p = 0.017). No relationship was found between apoptotic rates and age, gender or tumour grade. However, patients with tumours that showed higher AI values had a significantly lower disease-free survival (DFS) and overall survival (OS) than those with tumours that had lower AIs (p = 0.020 and p = 0.027). In a multivariate Cox proportional hazards model, AI remained a significant independent predictor of survival.

conclusionsWe conclude that disregulated apoptosis is an important event during CRC development and progression. Higher AIs are associated with more aggressive tumours and a poorer prognosis for patients with CRC.

Identifiers

PMID24106912
PMCPMC3852032

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Registered trials

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.