Evidence map›Paper›PMID 40891511›Full record

ArticleJournal of cellular biochemistry2025

Current Advances in Anticancer Properties of Heptamethine Carbocyanine DZ-1 Conjugated to Artesunate: Generation of Reactive Oxygen Species.

Badrinath Narayanasamy, Sarah Helmueller, Yi Zhang, Yong J Lee

Abstract read
In one paragraph

Article in Journal of cellular biochemistry, 2025. 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. Article
  2. Implications of the molecular toxicity and cytocompatibility by the nano-caged CNaunyn-Schmiedeberg's archives of pharmacology · 2026
    Article
  3. 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

4 authors.

Badrinath NarayanasamyDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Sarah HelmuellerDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA.ORCID 0009-0003-9164-0459
Yi ZhangDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Yong J LeeDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, California, USA.ORCID 0000-0001-5914-8489

Funding

Assessment of hyperthermia-based multimodal approach for hepatic colorectal metastasesR01CA265827 · NCI · CEDARS-SINAI MEDICAL CENTER · PI YONG JUN LEE · 2023 to 2026
$1.8M
ROS Targeted Therapy for Lethal Prostate CancerR21CA256419 · NCI · CEDARS-SINAI MEDICAL CENTER · PI WANG, RUOXIANG, ZHANG, YI · 2021 to 2022
$425k
Application of in vivo humanized PDX mouse model and ex vivo organoid model to assess the therapeutic efficacy of combinatorial therapy for pseudomyxoma peritoneiR21CA259243 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEE, YONG J · 2022 to 2023
$412k
NCI NIH HHS R01 CA265827NCI NIH HHS R21 CA256419NCI NIH HHS R21 CA259243
6 · The paper itself

Abstract

Heptamethine cyanine dyes and anticancer agents based conjugates are being developed for enhanced targeting and killing of cancer cells. DZ-1 dye conjugated agents induced cytotoxicity and mechanism of action have been shown in previous studies. In this study, a conjugated form of DZ-1 and artesunate (DZ-1-ART) was used to evaluate its cytotoxicity and elucidate the mechanism of actions in various cancer cell lines. Cells survival assays indicated dose-dependent cytotoxic activities of DZ-1-ART in HCT116, BxPC-3, and OVCAR-3 cell lines. Immunoblotting and terminal deoxynucleotidyl transferase dUTP nick-end labeling assay confirmed involvement of apoptosis in DZ-1-ART-induced cytotoxicity. To elucidate the anticancer mechanism of the action of DZ-1-ART, MitoTracker and JC-1 assay were used. The results showed that translocation of DZ-1-ART in the mitochondria was followed by disruption of mitochondrial outer membrane potential. Dichlorofluorescin diacetate assay confirmed the generation of reactive oxygen species (ROS) in DZ-1-ART treated cancer cells. An antioxidant, N-acetyl cysteine treatment with DZ-1-ART showed reduction in cell death as well as suppression of ROS generation. When compared to HCT116 wild-type cells, Bak and Bax-deficient HCT116 cells also showed similar levels of cytotoxicity of DZ-1-ART. Taken together, this study's results reported that DZ-1-ART could induce mitochondria-mediated, ROS-generated, and Bak and Bax-independent apoptosis in cancer cells.

Indexed as

Antineoplastic AgentsArtemisininsCarbocyaninesReactive Oxygen SpeciesApoptosisArtesunateCell Line, TumorCell SurvivalHCT116 CellsHumansMembrane Potential, MitochondrialMitochondriaAntineoplastic AgentsArtemisininsArtesunateCarbocyaninesReactive Oxygen Speciesartesunateheptamethine carbocyanine DZ‐1mitochondriaoxidative stressreactive oxygen species

Identifiers

PMID40891511
PMCPMC12706113

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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.