Recent Advances in Cancer Diagnosis and Therapy

A special issue of Pharmaceuticals (ISSN 1424-8247). This special issue belongs to the section "Pharmacology".

Deadline for manuscript submissions: 30 July 2025 | Viewed by 1001

Special Issue Editors


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Guest Editor
Department of Histology, University of Medicine and Pharmacy "Gr. T. Popa” Iasi, Iasi, Romania
Interests: obesity-related pathology; tumor pathology; histology
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Guest Editor
Department of Toxicology and Cancer Biology, College of Medicine, University of Kentucky, Lexington, KY, USA
Interests: drug resistance; cancer; signaling pathways; natural products

Special Issue Information

Dear Colleagues,

According to the World Health Organization report, cancer continues to be one of the leading causes of death worldwide. A cancer diagnosis is often made in advanced stages when it is associated with a high risk of recurrence and metastasis. Thus, the early diagnosis of cancer is one the most significant strategies to decrease the cancer mortality rate. Currently, the approach for cancer diagnosis includes non-invasive imaging exams combined with molecular biology techniques and the pathological examination of tissue samples to establish the type and stage of the cancer. In addition, another main cancer-related research priority is to develop new therapeutic tools with a high response rate and limited side-effects.

This Special Issue aims to provide a platform for gathering updated research in cancer-related diagnosis and treatment, which may improve the prognosis of the oncologic patient.

Dr. Adriana Grigoraș
Dr. Hsin-Sheng Yang
Guest Editors

Manuscript Submission Information

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Keywords

  • early diagnosis
  • advanced therapy
  • biomarkers
  • immunohistochemistry
  • molecular diagnosis
  • metastasis
  • prognosis
  • targeted therapies
  • combination therapies
  • cancer pharmacology

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Published Papers (1 paper)

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Research

20 pages, 6012 KiB  
Article
Novel Anthraquinone Derivatives and Their Complexes with Metal Ions with Anticancer Activity: Structure/Redox and Chelation Activity Correlations
by Olga Yu. Selyutina, Maya A. Ul’yanova, Olga A. Chinak, Viktor A. Timoshnikov, Lidiya G. Fedenok, Alexander A. Stepanov, Vadim V. Yanshole, Leonid V. Kulik, Sergey F. Vasilevsky, Nikolay E. Polyakov and George J. Kontoghiorghes
Pharmaceuticals 2024, 17(12), 1717; https://doi.org/10.3390/ph17121717 - 19 Dec 2024
Viewed by 670
Abstract
Background/Objectives: Some specific anthraquinone derivatives (AQs) are known to be used widely as effective chemotherapeutic agents in the treatment of cancer. However, their fundamental shortcoming is the high rate of cardiotoxicity observed in treated patients, which is thought to be caused by the [...] Read more.
Background/Objectives: Some specific anthraquinone derivatives (AQs) are known to be used widely as effective chemotherapeutic agents in the treatment of cancer. However, their fundamental shortcoming is the high rate of cardiotoxicity observed in treated patients, which is thought to be caused by the increase in production of reactive oxygen species (ROS) catalyzed by iron and copper. The development of improved AQs and other anticancer drugs with enhanced efficacy but reduced toxicity remains a high priority. The aim of this study was to evaluate the cytotoxic and ROS production effects of chelate iron and copper complexes of two novel AQs, namely 4-hydroxynaphto[2,3-h]cinnoline-7,12-dione (Q2) and 3-(hydroxymethyl)naphto[2,3-h]cinnoline-4,7,12(1H)-trione (Q3). Methods: The chelation ability of Q2 and Q3 was studied using NMR and UV–Vis spectroscopy. Cytotoxicity studies were carried out using the MTT assay. The influence of chelation on ROS production was studied using NMR spectroscopy in linoleic acid micelles. Results: It was found that only Q3 forms complexes with Fe(III) and Cu(II) ions, whereas Q2 does not demonstrate chelating properties. A cytotoxicity study revealed that Fe[Q3]3 significantly decreased the viability of lung cancer A549 cells, while Q3 and Cu[Q3]2 did not demonstrate cytotoxic properties in this cell line. Furthermore, the presence of Q3 lowered the rate of iron-induced lipid peroxidation in linoleic acid micelles. By contrast, Q2 did not influence the rate of lipid peroxidation, probably due to the absence of effective metal chelating ability. Conclusions: The high cytotoxic effects observed with the iron complex of Q3 against cancer cells in combination with a reduced rate of iron induced lipid peroxidation in the presence of Q3, make Q3 and its iron complex promising for further evaluation and use as chemotherapeutic agents in cancer. Full article
(This article belongs to the Special Issue Recent Advances in Cancer Diagnosis and Therapy)
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