Evidence map›Paper›PMID 36046085›Full record

ReviewExploration of targeted anti-tumor therapy2021

Aptamers and antibodies: rivals or allies in cancer targeted therapy?

Lisa Agnello, Simona Camorani, Monica Fedele, Laura Cerchia

Open access · diamondAbstract readReview
In one paragraph

Review in Exploration of targeted anti-tumor therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
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

26 citing papers in PubMed, 33 citations in OpenAlex.

  1. Design, Synthesis and Biophysical Characterisation of CPP-PNA Conjugates for Targeting Oncogenic microRNA-221.Journal of peptide science : an official publication of the European Peptide Society · 2026
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  12. Methods for cell- and tissue-specific DNA aptamer selection.Molecular therapy. Methods & clinical development · 2025
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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 at 1 institution in 2 countries.

Lisa Agnello *Institute of Experimental Endocrinology and Oncology "Gaetano Salvatore", National Research Council (CNR), Via S. Pansini 5, 80131 Naples, Italy.ORCID https://orcid.org/0000-0001-5923-1987
Simona Camorani *Institute of Experimental Endocrinology and Oncology "Gaetano Salvatore", National Research Council (CNR), Via S. Pansini 5, 80131 Naples, Italy.ORCID https://orcid.org/0000-0003-1144-0485
Monica FedeleInstitute of Experimental Endocrinology and Oncology "Gaetano Salvatore", National Research Council (CNR), Via S. Pansini 5, 80131 Naples, Italy.ORCID https://orcid.org/0000-0002-9171-1312
Laura CerchiaInstitute of Experimental Endocrinology and Oncology "Gaetano Salvatore", National Research Council (CNR), Via S. Pansini 5, 80131 Naples, Italy.ORCID https://orcid.org/0000-0002-7633-7932
Department of Physics, Mathematics and Informatics · BY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The goal of an efficacious cancer therapy is to specifically target diseased cells at high accuracy while sparing normal, healthy cells. Over the past three decades, immunotherapy, based on the use of monoclonal antibodies (mAbs) directed against tumor-associated antigens, to inhibit their oncogenic function, or against immune checkpoints, to modulate specific T cell responses against cancer, has proven to be an important strategy for cancer therapy. Nevertheless, the number of mAbs approved for clinical use is still limited because of significant drawbacks to their applicability. Oligonucleotide aptamers, similarly to antibodies, form high-affinity bonds with their specific protein targets, thus representing an effective tool for active cancer targeting. Compared to antibodies, aptamers' use as therapeutic agents benefits from their low size, low/no immunogenicity, simple synthesis and design flexibility for improving efficacy and stability. This review intends to highlight recently emerged applications of aptamers as recognition elements, from biomarker discovery to targeted drug delivery and targeted treatment, showing aptamers' potential to work in conjunction with antibodies for attacking cancer from multiple flanks.

Indexed as

Aptamersmonoclonal antibodiesSELEXtargeted therapytheranostics

Identifiers

PMID36046085
PMCPMC9400792
OpenAlexW3134066060

What OpenQuestion 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 OpenQuestion graph.