Evidence map›Paper›PMID 42611162›Full record

ReviewCell biochemistry and biophysics2026

Nanobodies Open New Avenues in Cancer Treatment: From Molecular Engineering to Therapeutic Platforms.

Glenda Romero-Hernández, Mario S Valdés-Tresanco, Ernesto Moreno

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cell biochemistry and biophysics, 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

3 authors.

Glenda Romero-HernándezDepartment of Biological Sciences, University of Calgary, Calgary, Alberta, Canada. glenda.romerohernand@ucalgary.ca.ORCID http://orcid.org/0000-0002-0172-5041
Mario S Valdés-TresancoInstitute of Basic Sciences, Faculty of Engineering, University of Medellin, Medellin, Colombia.ORCID http://orcid.org/0000-0002-1291-1587
Ernesto MorenoInstitute of Basic Sciences, Faculty of Engineering, University of Medellin, Medellin, Colombia. emoreno@udemedellin.edu.co.ORCID http://orcid.org/0000-0002-2309-4826

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanobody technology is a promising approach in cancer research and treatment. Monoclonal antibodies have long been central to targeted therapies; however, their large size, complex production, and limited tissue penetration restrict their clinical performance. Nanobodies, derived from camelid heavy-chain antibodies, possess unique properties, including small size (~15 kDa), high stability, and the ability to access otherwise inaccessible epitopes. At the molecular and cellular levels, these characteristics arise from a defined structure-function relationship that governs antigen binding, receptor modulation, and downstream signaling. Beyond affinity, nanobody function is influenced by binding kinetics and intracellular trafficking. Their ease of production in bacterial systems further enhances cost-effectiveness compared to conventional antibodies. Nanobody-based strategies have evolved from diagnostic and imaging tools to multifunctional therapeutic platforms, including nanobody-drug conjugates, bispecific and multispecific engagers, immune checkpoint modulators, and engineered cell-based therapies such as CAR-T systems. Preclinical studies have demonstrated improved tumor targeting, enhanced immune activation, and reduced off-target effects. Emerging clinical evidence, including approved nanobody therapeutics and ongoing trials, supports their safety, feasibility, and translational potential in cancer patients. Together, these findings highlight nanobodies as versatile platforms capable of overcoming key limitations of conventional therapies and facilitating clinical translation in precision oncology.

Indexed as

NeoplasmsProtein EngineeringSingle-Domain AntibodiesAnimalsHumansSingle-Domain AntibodiesCancer therapyNanobodiesNanobody engineeringNanomedicine

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.