Evidence map›Paper›PMID 24587670›Full record

ReviewWorld journal of gastroenterology2014

Targeting cell death signaling in colorectal cancer: current strategies and future perspectives.

Bruno Christian Koehler, Dirk Jäger, Henning Schulze-Bergkamen

Open access · bronzeAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Aging · 2021
    Article
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  9. Review
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  15. Mitochondrial DNA variants in colorectal carcinogenesis: Drivers or passengers?Journal of cancer research and clinical oncology · 2017
    Review
  16. Article
  17. Review
  18. Article
  19. 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

3 authors at 1 institution in 1 country.

Bruno Christian KoehlerBruno Christian Koehler, Dirk Jäger, Henning Schulze-Bergkamen, National Center for Tumor Diseases, University Hospitals Heidelberg, 69120 Heidelberg, Germany.
Dirk JägerBruno Christian Koehler, Dirk Jäger, Henning Schulze-Bergkamen, National Center for Tumor Diseases, University Hospitals Heidelberg, 69120 Heidelberg, Germany.
Henning Schulze-BergkamenBruno Christian Koehler, Dirk Jäger, Henning Schulze-Bergkamen, National Center for Tumor Diseases, University Hospitals Heidelberg, 69120 Heidelberg, Germany.
Heidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The evasion from controlled cell death induction has been considered as one of the hallmarks of cancer cells. Defects in cell death signaling are a fundamental phenomenon in colorectal cancer. Nearly any non-invasive cancer treatment finally aims to induce cell death. However, apoptosis resistance is the major cause for insufficient therapeutic success and disease relapse in gastrointestinal oncology. Various compounds have been developed and evaluated with the aim to meet with this obstacle by triggering cell death in cancer cells. The aim of this review is to illustrate current approaches and future directions in targeting cell death signaling in colorectal cancer. The complex signaling network of apoptosis will be demonstrated and the "druggability" of targets will be identified. In detail, proteins regulating mitochondrial cell death in colorectal cancer, such as Bcl-2 and survivin, will be discussed with respect to potential therapeutic exploitation. Death receptor signaling and targeting in colorectal cancer will be outlined. Encouraging clinical trials including cell death based targeted therapies for colorectal cancer are under way and will be demonstrated. Our conceptual understanding of cell death in cancer is rapidly emerging and new types of controlled cellular death have been identified. To meet this progress in cell death research, the implication of autophagy and necroptosis for colorectal carcinogenesis and therapeutic approaches will also be depicted. The main focus of this topic highlight will be on the revelation of the complex cell death concepts in colorectal cancer and the bridging from basic research to clinical use.

Indexed as

ApoptosisAutophagyCarcinogenesisCarcinomaCell DeathColorectal NeoplasmsHumansInhibitor of Apoptosis ProteinsMitochondriaNecrosisProto-Oncogene Proteins c-bcl-2Receptors, Tumor Necrosis FactorRecurrenceSignal TransductionSurvivinTNF-Related Apoptosis-Inducing LigandBIRC5 protein, humanInhibitor of Apoptosis ProteinsProto-Oncogene Proteins c-bcl-2Receptors, Tumor Necrosis FactorSurvivinTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanApoptosisAutophagyBcl-2 proteinsBH-3 mimeticsClinical trialColorectal cancerInflammatory bowel diseaseNecroptosis

Identifiers

PMID24587670
PMCPMC3934462
OpenAlexW1995784978

What OpenQuestion holds

Textmetadata
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.