Evidence map›Paper›PMID 34440171›Full record

ArticleBiomedicines2021

Core Circadian Clock Proteins as Biomarkers of Progression in Colorectal Cancer.

María I Aroca-Siendones, Sara Moreno-SanJuan, Jose D Puentes-Pardo, Michela Verbeni, Javier Arnedo, Julia Escudero-Feliu, María García-Costela, Adelina García-Robles, Ángel Carazo, Josefa León

Abstract read
In one paragraph

Article in Biomedicines, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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.

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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Circadian rhythm disruption and endocrine-related tumors.World journal of clinical oncology · 2024
    Review
  9. Review
  10. Article
  11. Review
  12. Article
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

10 authors.

María I Aroca-SiendonesBiobank of the Public Health System of Andalusia, 18016 Granada, Spain.
Sara Moreno-SanJuanCytometry and Microscopy Research Service, Biosanitary Research Institute of Granada (ibs.GRANADA), 18012 Granada, Spain.
Jose D Puentes-PardoBiosanitary Research Institute of Granada (ibs.GRANADA), 18012 Granada, Spain.ORCID 0000-0002-6417-6019
Michela VerbeniDepartment of Computer Science and Artificial Intelligence, University of Granada, 18071 Granada, Spain.
Javier ArnedoBioinformatics Service, Instituto de Investigación Biosanitaria de Granada, ibs.GRANADA, 18012 Granada, Spain.ORCID 0000-0002-0380-5248
Julia Escudero-FeliuBiosanitary Research Institute of Granada (ibs.GRANADA), 18012 Granada, Spain.
María García-CostelaBiosanitary Research Institute of Granada (ibs.GRANADA), 18012 Granada, Spain.
Adelina García-RoblesBiosanitary Research Institute of Granada (ibs.GRANADA), 18012 Granada, Spain.
Ángel CarazoBiosanitary Research Institute of Granada (ibs.GRANADA), 18012 Granada, Spain.
Josefa LeónBiosanitary Research Institute of Granada (ibs.GRANADA), 18012 Granada, Spain.ORCID 0000-0002-0543-4823

Funding

Instituto de Salud Carlos III PI18/01947Ministerio de Economía, Industria y Competitividad, Gobierno de España DPI2017-84439-R
6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the most common tumours in developed countries. Although its incidence and mortality rates have decreased, its prognosis has not changed, and a high percentage of patients with CRC develop relapse (metachronous metastasis, MM, or local recurrence, LR) during their disease. The identification of these patients is very important for their correct management, but the lack of prognostic markers makes it difficult. Given the connection between circadian disruption and cancer development and progression, we aimed to analyse the prognostic significance of core circadian proteins in CRC. We measured the expression of PER1-3, CRY1-2, BMAL1 and NR1D2 in a cohort of CRC patients by immunohistochemistry (IHC) and analysed their prognostic potential in this disease. A low expression of PER2 and BMAL1 was significantly associated with metastasis at the moment of disease diagnosis, whereas a high expression of CRY1 appeared as an independent prognostic factor of MM development. A high expression of NR1D2 appeared as an independent prognostic factor of LR development after disease diagnosis. Moreover, patients with a low expression of BMAL1 and a high expression of CRY1 showed lower OS and DFS at five years. Although these markers need to be validated in larger and different ethnic cohorts, the simplicity of IHC makes these proteins candidates for personalizing CRC treatment.

Indexed as

colorectal cancercore circadian clockdisease free survivallocal recurrencemetachronous metastasisoverall survival

Identifiers

PMID34440171
PMCPMC8391187

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.