Evidence mapPaperPMID 40141362Full record

ReviewInternational journal of molecular sciences2025

Prolonged Low-Dose Administration of FDA-Approved Drugs for Non-Cancer Conditions: A Review of Potential Targets in Cancer Cells.

Olivia Chang, Sarah Cheon, Nina Semenova, Neelam Azad, Anand Krishnan Iyer, Juan Sebastian Yakisich

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Olivia ChangGovernor's School for Science and Technology, Hampton, VA 23666, USA.ORCID 0000-0003-1545-1376
Sarah CheonGovernor's School for Science and Technology, Hampton, VA 23666, USA.ORCID 0009-0009-6457-0727
Nina SemenovaDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA 23668, USA.
Neelam AzadThe Office of the Vice President for Research, Hampton University, Hampton, VA 23668, USA.
Anand Krishnan IyerDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA 23668, USA.
Juan Sebastian YakisichDepartment of Pharmaceutical Sciences, School of Pharmacy, Hampton University, Hampton, VA 23668, USA.

Funding

NIH HHS HU-180004
6 · The paper itself

Abstract

Though not specifically designed for cancer therapy, several FDA-approved drugs such as metformin, aspirin, and simvastatin have an effect in lowering the incidence of cancer. However, there is a great discrepancy between in vitro concentrations needed to eliminate cancer cells and the plasma concentration normally tolerated within the body. At present, there is no universal explanation for this discrepancy and several mechanisms have been proposed including targeting cancer stem cells (CSCs) or cellular senescence. CSCs are cells with the ability of self-renewal and differentiation known to be resistant to chemotherapy. Senescence is a response to damage and stress, characterized by permanent cell-cycle arrest and apoptotic resistance. Although, for both situations, there are few examples where low concentrations of the FDA-approved drugs were the most effective, there is no satisfactory data to support that either CSCs or cellular senescence are the target of these drugs. In this review, we concisely summarize the most used FDA-approved drugs for non-cancer conditions as well as their potential mechanisms of action in lowering cancer incidence. In addition, we propose that prolonged low-dose administration (PLDA) of specific FDA-approved drugs can be useful for effectively preventing metastasis formation in selected patients.

Indexed as

Antineoplastic AgentsNeoplasmsAnimalsCellular SenescenceDrug ApprovalHumansNeoplastic Stem CellsUnited StatesUnited States Food and Drug AdministrationAntineoplastic Agentscarcinogenesis metastasischemopreventionplasticitysenescencestem cells

Identifiers

PMID40141362
PMCPMC11942989

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.