Evidence map›Paper›PMID 31195370›Full record

ArticleAging2019

Immune senescence and immune activation in elderly colorectal cancer patients.

Silvia Giunco, Maria Raffaella Petrara, Francesca Bergamo, Paola Del Bianco, Marisa Zanchetta, Francesco Carmona, Vittorina Zagonel, Anita De Rossi, Sara Lonardi

Abstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Observational
  6. Article
  7. Article
  8. Article
  9. Article
  10. Cellular Senescence, Inflammation, and Cancer in the Gastrointestinal Tract.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Observational
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.

Silvia Giunco *Section of Oncology and Immunology, Department of Surgery, Oncology and Gastroenterology - DiSCOG, University of Padova, Padova 35128, Italy.
Maria Raffaella Petrara *Section of Oncology and Immunology, Department of Surgery, Oncology and Gastroenterology - DiSCOG, University of Padova, Padova 35128, Italy.
Francesca BergamoMedical Oncology Unit 1, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.
Paola Del BiancoClinical trials and Biostatistic Unit, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.
Marisa ZanchettaImmunology and Molecular Oncology Unit, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.
Francesco CarmonaImmunology and Molecular Oncology Unit, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.
Vittorina ZagonelMedical Oncology Unit 1, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.
Anita De RossiSection of Oncology and Immunology, Department of Surgery, Oncology and Gastroenterology - DiSCOG, University of Padova, Padova 35128, Italy.
Sara LonardiMedical Oncology Unit 1, Veneto Institute of Oncology IOV - IRCCS, Padova 35128, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In our previous study, we found that low thymic output and short telomere length were associated with a higher risk of tumor in elderly cancer patients. Here, we aimed to examine in depth the impact of immunological and biological senescence and immune activation on disease outcome in elderly patients with colorectal cancer (CRC).Peripheral blood samples from 81 CRC patients were studied for immune activation, immune senescence and recent thymic emigrant(RTE) CD4 and CD8 cells by flow cytometry. T-cell receptor rearrangement excision circle (TREC) levels and telomere lengths were measured by real-time PCR. Plasma levels of microbial translocation markers, LPS and sCD14, were quantified by ELISA. While TREC levels and telomere length were not prognostic of disease outcome, high percentages of immune senescent and immune activated CD8 cells were associated with a higher risk of a negative event (relapse, progression, or death) in all studied patients and disease relapse in I-III staged patients. Levels of sCD14 and LPS were higher in patients who will experience a negative event than in patients who will not. In conclusion, in elderly CRC patients higher immunological senescence and immune activation negatively impact the disease outcome; how these characteristics influence the antineoplastic treatments remains to be investigated.

Indexed as

AgedAged, 80 and overBiomarkersCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesColorectal NeoplasmsFemaleFlow CytometryHumansMaleTelomereBiomarkerscolorectal cancerelderlyimmune senescenceinflammation/immune activation

Identifiers

PMID31195370
PMCPMC6594805

What OpenQuestion holds

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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.