Evidence map›Paper›PMID 40682710›Full record

ReviewMolecular and cellular biochemistry2025

Balancing senescence and apoptosis: therapeutic insights into aging and cancer.

Nusrat Jan, Shazia Sofi, Aijaz Ahmad Mir, Gowhar Masoodi, Manzoor Ahmad Mir

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Molecular and cellular biochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Nusrat JanCancer Biology Laboratory, Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, 190006, India.
Shazia SofiCancer Biology Laboratory, Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, 190006, India.
Aijaz Ahmad MirCancer Biology Laboratory, Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, 190006, India.
Gowhar MasoodiCancer Biology Laboratory, Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, 190006, India.
Manzoor Ahmad MirCancer Biology Laboratory, Department of Bioresources, School of Biological Sciences, University of Kashmir, Srinagar, 190006, India. drmanzoor@kashmiruniversity.ac.in.ORCID http://orcid.org/0000-0003-3297-1402

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging and cancer are interconnected processes resulting from irreversible dysfunctions, primarily caused by stress-induced DNA and cellular damage. While aging is characterized by the accumulation of senescent cells (SnCs), cancer development is linked to a progressive decline in the ability of cells to undergo senescence and apoptosis. Both processes serve as crucial tumor suppressor mechanisms in early life but may contribute to aging-related pathologies over time. Cellular senescence and apoptosis are stress responses that play vital roles in maintaining tissue homeostasis. In aging, SnCs accumulate in tissues due to dysregulated apoptotic pathways, while in cancer, reduced senescence and apoptosis enable uncontrolled proliferation. Recent findings suggest that several anticancer drugs, including classical apoptosis inducers, can also promote senescence, highlighting the potential for pro-senescence strategies in cancer therapy. Understanding the mechanistic pathways and biomarkers of these processes can provide insight into their interplay and their impact on disease progression. Exploring the balance between cellular senescence and apoptosis may lead to novel therapeutic approaches for both aging and cancer. Targeting these mechanisms could help develop anti-aging and anticancer treatments with minimized adverse effects, offering promising avenues for future research and clinical applications.

Indexed as

AgingAntineoplastic AgentsApoptosisCellular SenescenceNeoplasmsAnimalsHumansAntineoplastic AgentsAgingApoptosisBCL2 familyOncogenesPrognosisSenescenceSenolytics

Identifiers

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.