Evidence map›Paper›PMID 39126015›Full record

ReviewInternational journal of molecular sciences2024

Therapy-Induced Senescence: Novel Approaches for Markers Identification.

Francesco Pacifico, Fulvio Magni, Antonio Leonardi, Elvira Crescenzi

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

4 authors.

Francesco PacificoIstituto per l'Endocrinologia e l'Oncologia Sperimentale, CNR, Via S. Pansini 5, 80131 Naples, Italy.ORCID 0000-0001-9563-3596
Fulvio MagniProteomics and Metabolomics Unit, Department of Medicine and Surgery, University of Milano-Bicocca, 20854 Vedano al Lambro, Italy.ORCID 0000-0002-8663-0374
Antonio LeonardiDipartimento di Medicina Molecolare e Biotecnologie Mediche, University of Naples "Federico II", Via S. Pansini 5, 80131 Naples, Italy.ORCID 0000-0001-8636-9623
Elvira CrescenziIstituto per l'Endocrinologia e l'Oncologia Sperimentale, CNR, Via S. Pansini 5, 80131 Naples, Italy.ORCID 0000-0002-9258-8053

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapy-induced senescence (TIS) represents a major cellular response to anticancer treatments. Both malignant and non-malignant cells in the tumor microenvironment undergo TIS and may be harmful for cancer patients since TIS cells develop a senescence-associated secretory phenotype (SASP) that can sustain tumor growth. The SASP also modulates anti-tumor immunity, although the immune populations involved and the final results appear to be context-dependent. In addition, senescent cancer cells are able to evade senescence growth arrest and to resume proliferation, likely contributing to relapse. So, research data suggest that TIS induction negatively affects therapy outcomes in cancer patients. In line with this, new interventions aimed at the removal of senescent cells or the reprogramming of their SASP, called senotherapy, have become attractive therapeutic options. To date, the lack of reliable, cost-effective, and easy-to-use TIS biomarkers hinders the application of recent anti-senescence therapeutic approaches in the clinic. Hence, the identification of biomarkers for the detection of TIS tumor cells and TIS non-neoplastic cells is a high priority in cancer research. In this review article, we describe the current knowledge about TIS, outline critical gaps in our knowledge, and address recent advances and novel approaches for the discovery of TIS biomarkers.

Indexed as

Biomarkers, TumorCellular SenescenceNeoplasmsSenescence-Associated Secretory PhenotypeTumor MicroenvironmentAnimalsBiomarkersHumansSenotherapeuticsBiomarkersBiomarkers, TumorSenotherapeuticsbiomarkersSASPsenolyticssenotherapytherapy-induced senescence

Identifiers

PMID39126015
PMCPMC11313450

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.