Evidence map›Paper›PMID 39169897›Full record

ArticleThoracic cancer2024

Age-related features of lung cancer treatment using reprogrammed CD8 positive T cells in mice subjected to injection of Lewis lung carcinoma cells.

Evgenii Skurikhin, Mariia Zhukova, Natalia Ermakova, Edgar Pan, Darius Widera, Lubov Sandrikina, Lena Kogai, Nikolai Kushlinskii, Aslan Kubatiev, Sergey Morozov and 1 more

Abstract read
In one paragraph

Article in Thoracic cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Evgenii SkurikhinInstitute of General Pathology and Pathophysiology, Moscow, Russia.ORCID 0000-0001-7445-4767
Mariia ZhukovaInstitute of General Pathology and Pathophysiology, Moscow, Russia.
Natalia ErmakovaInstitute of General Pathology and Pathophysiology, Moscow, Russia.
Edgar PanInstitute of General Pathology and Pathophysiology, Moscow, Russia.ORCID 0000-0002-2163-7647
Darius WideraStem Cell Biology and Regenerative Medicine Group, School of Pharmacy, Whiteknights Campus, Reading, UK.
Lubov SandrikinaGoldberg ED Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Centre of the Russian Academy of Sciences, Tomsk, Russia.
Lena KogaiGoldberg ED Research Institute of Pharmacology and Regenerative Medicine, Tomsk National Research Medical Centre of the Russian Academy of Sciences, Tomsk, Russia.
Nikolai KushlinskiiBlokhin National Medical Research Center of Oncology, Moscow, Russia.
Aslan KubatievInstitute of General Pathology and Pathophysiology, Moscow, Russia.
Sergey MorozovInstitute of General Pathology and Pathophysiology, Moscow, Russia.
Alexander DygaiInstitute of General Pathology and Pathophysiology, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAwareness of age-related features of carcinogenesis and the importance of cellular immunity is crucial for developing effective antitumor therapies for specific patient groups.

methodsIn this study, we examined different populations of cancer stem cells (CSCs) and circulating tumor cells (CTCs) in "young" (8-10 weeks) and "aged" (80-82 weeks) C57BL/6 male mice. We used an orthotopic model of Lewis lung carcinoma (LLC) to evaluate the effectiveness of cell therapy targeting lung cancer through reprogrammed CD8-positive T cells (rCD8+ T cells) in mice from two different ages.

resultsThe findings revealed that tumor progression with age is primarily caused by impaired recruitment of T cells to the lungs. Additionally, a lower number of CTCs and CSCs were observed in younger mice compared to the older mice. The antitumor effect of rCD8+ T cells in aged mice was found to be inferior to that in young mice, which can be attributed to the reduced impact of therapy on specific CSCs populations.

conclusionsThese results offer new insights into the treatment of lung cancer using rCD8+ T cells. Considering the age-related characteristics influencing disease progression, this therapy has the potential to significantly enhance the effectiveness of treatment methods.

Indexed as

Carcinoma, Lewis LungCD8-Positive T-LymphocytesLung NeoplasmsAge FactorsAnimalsDisease Models, AnimalHumansMaleMiceMice, Inbred C57BLNeoplastic Cells, CirculatingNeoplastic Stem Cellsaged and young micecancer stem cellscell therapycirculating tumor cellsreprogrammed CD8+ T cells

Identifiers

PMID39169897
PMCPMC11444928

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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.