Recent Development of Anticancer Agents

A special issue of Applied Sciences (ISSN 2076-3417). This special issue belongs to the section "Applied Biosciences and Bioengineering".

Deadline for manuscript submissions: closed (10 September 2022) | Viewed by 5957

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Dipartimento di Scienze Chimiche e Geologiche, Università degli Studi di Modena e Reggio Emilia, 41125 Modena, Italy
Interests: medicinal chemistry; organic synthesis; drug discovery
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Special Issue Information

Dear Colleagues,

Recent fundamental breakthroughs in the understanding of the molecular mechanisms regulating the development and spread of tumours and the immune response to cancer have led to an increasing number and variety of cancer therapies. The options available to cancer patients now include immunotherapy and targeted therapy alongside classical endocrine, radiation and chemo therapies. There is, however, a pressing medical need linked to the intrinsic or acquired resistance to cancer drugs. Drug resistance is still responsible for most relapses of cancer, and is one of the major causes of death of the disease. Current cancer research is often aimed at the development of therapeutic agents for cancer treatment that will also be able to overcome drug resistance.

This Special Issue, “Recent Development of Anticancer Agents”, will focus on original research articles and reviews on the drug discovery and development process translating basic research in new anticancer therapies, with a particular focus on the elucidation of the molecular mechanisms involved in neoplastic processes and the development of small molecule inhibitors for cancer treatment.

Prof. Dr. Alfonso Zambon
Guest Editor

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Keywords

  • small molecule inhibitors
  • cancer therapy
  • cancer drug resistance
  • drug discovery

Published Papers (2 papers)

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Research

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19 pages, 7275 KiB  
Article
Anticancer Activity of Some Ruthenium(III) Complexes with Quinolone Antibiotics: In Vitro Cytotoxicity, Cell Cycle Modulation, and Apoptosis-Inducing Properties in LoVo Colon Cancer Cell Line
by Mirela Mihaila, Camelia Mia Hotnog, Marinela Bostan, Alexandra Cristina Munteanu, Ileana Adela Vacaroiu, Lorelei Irina Brasoveanu and Valentina Uivarosi
Appl. Sci. 2021, 11(18), 8594; https://doi.org/10.3390/app11188594 - 16 Sep 2021
Cited by 8 | Viewed by 1674
Abstract
Cisplatin is one of the most effective anticancer agents used to treat colon cancer, which is the third malignancy between the most common human cancers in the world, but the resistance developed represents an obstacle against the full success of chemotherapy. An emerging [...] Read more.
Cisplatin is one of the most effective anticancer agents used to treat colon cancer, which is the third malignancy between the most common human cancers in the world, but the resistance developed represents an obstacle against the full success of chemotherapy. An emerging interest appeared in finding other metallic compounds, such as ruthenium(III) complexes, for chemotherapeutic application in cancer. Our study focused on the anticancer activity of several ruthenium (Ru) complexes with quinolone antibiotics in colon tumor cell cultures. Real-time cell analysis and drug-mediated cytotoxicity tests monitored the inhibitory effects in the drug-treated LoVo colon cancer cells. Flow cytometry assays were performed to evaluate cell cycle phases distribution and apoptotic events. The obtained results showed dose-dependent increased levels of cell lysis and induction of apoptosis in LoVo cancer cells treated with the Ru(III) complexes. In addition, data showed a major decrease in cell proliferation, since the percentages of cells distributed in the S cell cycle phase diminished, and a G0/G1 cell arrest was observed. Therefore, our results strongly suggest that the newly synthesized Ru(III) complexes might play an important role in future chemotherapeutic approaches, since their activity is based on diminishing cell proliferation, induction of apoptosis, and modulation of cell cycle phases. Full article
(This article belongs to the Special Issue Recent Development of Anticancer Agents)
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Review

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17 pages, 1090 KiB  
Review
Phytochemicals Block Glucose Utilization and Lipid Synthesis to Counteract Metabolic Reprogramming in Cancer Cells
by Qiong Wu, Bo Zhao, Guangchao Sui and Jinming Shi
Appl. Sci. 2021, 11(3), 1259; https://doi.org/10.3390/app11031259 - 29 Jan 2021
Cited by 5 | Viewed by 3625
Abstract
Aberrant metabolism is one of the hallmarks of cancers. The contributions of dysregulated metabolism to cancer development, such as tumor cell survival, metastasis and drug resistance, have been extensively characterized. “Reprogrammed” metabolic pathways in cancer cells are mainly represented by excessive glucose consumption [...] Read more.
Aberrant metabolism is one of the hallmarks of cancers. The contributions of dysregulated metabolism to cancer development, such as tumor cell survival, metastasis and drug resistance, have been extensively characterized. “Reprogrammed” metabolic pathways in cancer cells are mainly represented by excessive glucose consumption and hyperactive de novo lipogenesis. Natural compounds with anticancer activities are constantly being demonstrated to target metabolic processes, such as glucose transport, aerobic glycolysis, fatty acid synthesis and desaturation. However, their molecular targets and underlying anticancer mechanisms remain largely unclear or controversial. Mounting evidence indicated that these natural compounds could modulate the expression of key regulatory enzymes in various metabolic pathways at transcriptional and translational levels. Meanwhile, natural compounds could also inhibit the activities of these enzymes by acting as substrate analogs or altering their protein conformations. The actions of natural compounds in the crosstalk between metabolism modulation and cancer cell destiny have become increasingly attractive. In this review, we summarize the activities of natural small molecules in inhibiting key enzymes of metabolic pathways. We illustrate the structural characteristics of these compounds at the molecular level as either inhibitor of various enzymes or regulators of metabolic pathways in cancer cells. Our ultimate goal is to both facilitate the clinical application of natural compounds in cancer therapies and promote the development of novel anticancer therapeutics. Full article
(This article belongs to the Special Issue Recent Development of Anticancer Agents)
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