Evidence map›Paper›PMID 39590321›Full record

ArticleCurrent issues in molecular biology2024

Preliminary Study on Lutetium-177 and Gold Nanoparticles: Apoptosis and Radiation Enhancement in Hepatic Cancer Cell Line.

Maria Anthi Kouri, Anastasios Georgopoulos, George E Manios, Eirini Maratou, Aris Spathis, Sofia Chatziioannou, Kalliopi Platoni, Efstathios P Efstathopoulos

Abstract read
In one paragraph

Article in Current issues in molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. [Wiener klinische Wochenschrift · 2026
    Article
  2. Combination therapy strategies in engineeredCell communication and signaling : CCS · 2026
    Review
  3. NeoadjuvantCancers · 2025
    Review
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

8 authors.

Maria Anthi Kouri2nd Department of Radiology, Medical Physics Unit, Medical School, National and Kapodistrian University of Athens, 1 Rimini Str., 12462 Athens, Greece.ORCID 0000-0002-3296-3317
Anastasios Georgopoulos2nd Department of Radiology, Medical Physics Unit, Medical School, National and Kapodistrian University of Athens, 1 Rimini Str., 12462 Athens, Greece.
George E Manios2nd Department of Radiology, Medical Physics Unit, Medical School, National and Kapodistrian University of Athens, 1 Rimini Str., 12462 Athens, Greece.
Eirini MaratouClinical Biochemistry Laboratory, Attikon General Hospital, Medical School, National and Kapodistrian University of Athens, 12462 Athens, Greece.
Aris Spathis2nd Department of Pathology, School of Medicine, Attikon University Hospital, National and Kapoditrian University of Athens, 12462 Athens, Greece.ORCID 0000-0001-8867-3661
Sofia Chatziioannou2nd Department of Radiology, Medical Physics Unit, Medical School, National and Kapodistrian University of Athens, 1 Rimini Str., 12462 Athens, Greece.ORCID 0000-0002-8344-8219
Kalliopi Platoni2nd Department of Radiology, Medical Physics Unit, Medical School, National and Kapodistrian University of Athens, 1 Rimini Str., 12462 Athens, Greece.
Efstathios P Efstathopoulos2nd Department of Radiology, Medical Physics Unit, Medical School, National and Kapodistrian University of Athens, 1 Rimini Str., 12462 Athens, Greece.ORCID 0000-0003-2747-3353

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigates a novel approach toward enhancing the efficacy of Lutetium-177 (Lu-177) radiopharmaceutical therapy by combining it with gold nanoparticles (AuNPs) in the HepG2 hepatic cancer cell line. Lu-177, known for its effective β radiation, also emits gamma rays at energies (113 keV and 208 keV) near the photoelectric absorption range, suggesting potential for targeted and localized radiation enhancement when used in conjunction with AuNPs. Thus, HepG2 cells were treated at two different activity levels (74 MBq and 148 MBq), with Lu-177 alone, with a combination of Lu-177 and AuNPs in two sizes (10 nm and 50 nm), while some received no treatment. Treatment efficacy was assessed by quantifying the radiation enhancement ratio (RER) and the apoptosis levels. The results reveal that combining Lu-177 with AuNPs significantly increases cell death and apoptosis compared to Lu-177 alone, with 10 nm AuNPs demonstrating superior effectiveness. Additionally, varying Lu-177 activity levels influenced the treatment outcomes, with higher activity levels further augmenting the therapeutic impact of combined therapy. These findings underscore the potential of utilizing Lu-177's beta, but also gamma, emissions, traditionally considered non-therapeutic, for localized radiation enhancement when combined with AuNPs. This novel strategy leverages Lu-177 as an internal irradiator to exploit gamma radiation for a targeted therapeutic advantage without requiring nanoparticle functionalization. The study provides a promising approach to improving radionuclide therapy and sets the stage for future research aimed at optimizing cancer treatments through the combined use of Lu-177 and AuNPs.

Indexed as

apoptosisgold nanoparticlesgold nanospheresHepG2 cancer cell lineLutetium-177molecular therapyradiation enhancement ratio (RER)radionuclide therapyradiosensitization

Identifiers

PMID39590321
PMCPMC11592690

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Registered trials

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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.