Evidence map›Paper›PMID 41820318›Full record

ReviewAnti-cancer agents in medicinal chemistry2026

Aptamers in Osteosarcoma: New Paths for Diagnosis and Treatment.

Guy Awad, Marc Boutros, Antoine Chartouni, Juan Pretell-Mazzini

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In one paragraph

Review in Anti-cancer agents in medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Guy AwadFaculty of Medicine, Saint Joseph University, Beirut, Lebanon.ORCID 0009-0003-9902-7878
Marc BoutrosFaculty of Medicine, Saint Joseph University, Beirut, Lebanon.ORCID 0000-0003-1765-4222
Antoine ChartouniFaculty of Medicine, Saint Joseph University, Beirut, Lebanon.ORCID 0000-0002-8140-8520
Juan Pretell-MazziniMiami Cancer Institute, Baptist Health South Florida, Miami, FL, USA.ORCID 0000-0002-4893-0341

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOsteosarcoma remains the most common primary malignant bone tumor, with poor outcomes in metastatic or recurrent cases. Current treatments often fail to prevent relapse, highlighting the need for innovative therapeutic strategies. Aptamers, short and single-stranded oligonucleotides capable of folding into three-dimensional shapes, have emerged as promising tools for targeted cancer diagnostics and therapy due to their high affinity, specificity, and modifiability.

methodsA structured search was conducted through PubMed, Scopus, and Google Scholar up to March 2025, focusing on peer-reviewed articles exploring the use of aptamers in osteosarcoma. A total of 158 studies were included, highlighting aptamer applications in tumor diagnosis, pathway targeting, and precision drug delivery.

resultsAptamers demonstrated significant potential in osteosarcoma research, notably in identifying tumorigenesis pathways, enhancing diagnostic accuracy through ELISA and biosensors, and improving targeted drug delivery. SELEX-derived aptamers effectively targeted molecules such as CD133, EGFR, VEGFA, and FGFR1, leading to enhanced cytotoxicity, reduced off-target effects, and greater specificity for osteosarcoma cells and cancer stem cells. The integration of aptamers with nanoparticles further optimized therapeutic delivery, highlighting their capability to enhance precision medicine in osteosarcoma. DISCUSSION: Aptamers offer clear benefits over traditional osteosarcoma treatments. Their strong binding affinity to cancer cells, low risk of immune reactions, and flexible chemical modifications make them powerful tools for diagnosis and therapy, especially when combined with nanoparticle delivery systems.

conclusionAptamers represent a promising class of targeted agents for osteosarcoma. Future research should prioritize optimizing delivery strategies and validating clinical efficacy to accelerate their integration into clinical practice.

Indexed as

Antineoplastic AgentsAptamers, NucleotideBone NeoplasmsOsteosarcomaCell ProliferationDrug Screening Assays, AntitumorHumansSELEX Aptamer TechniqueAntineoplastic AgentsAptamers, Nucleotideaptamermolecular diagnosticsnanoparticle conjugatesOsteosarcomaprecision oncologyRNASELEXssDNAtargeted drug deliverytumorigenesis pathways

Identifiers

PMID41820318

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.