Advances in Medical Genetics, Genomics and Precision Medicine: From a Molecular Perspective to Clinical Practice

A special issue of Medicina (ISSN 1648-9144). This special issue belongs to the section "Genetics and Molecular Medicine".

Deadline for manuscript submissions: 31 July 2024 | Viewed by 830

Special Issue Editors


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Guest Editor
1. Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia
2. Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia
Interests: internal medicine; molecular medicine; medical genetics; medical genomics; hematology; medical oncology; molecular biology; endocrinology; endocrine oncology; precision medicine

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Guest Editor
Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia
Interests: mental health; cardiogenetics; genetic epidemiology; circadian rhythm; molecular biology research

Special Issue Information

Dear Colleagues,

The breathtaking developments in molecular diagnostics over the past decades and their translation to clinical practice have enabled insight into the pathophysiology of diseases that could only be recognized at the supracellular level until now. The introduction of molecular techniques for the detection of genetic and chromosomal disorders has opened up a range of possibilities for precise diagnostics. This progress also enables the development of completely new therapies with influence at the subcellular level, such as targeted therapy, immunotherapy, cell therapy and gene therapy. Nevertheless, its implementation is not without barriers, including difficulties in the assessment and interpretation of genomic data, deficient training of professionals in this field and unequal access to units with scientific expertise, as well as infrastructures necessary for the incorporation of genomic technologies.

The main aim of this Special Issue of Medicina will be to deliver new insight from the fields of molecular and cellular medicine that describe the impact of medical genetics- and genomics-disruptive innovations on the healthcare system in order to provide better diagnosis and treatment.

I invite colleagues around the world to report their experience and knowledge in medical genetics and genomics with basic, translational and clinical research, original studies, comparative studies, reviews, systematic reviews and meta-analyses. Only rare clinical entities and case reports that are novel are welcome.

Prof. Dr. Darko Katalinić
Dr. Ivana Škrlec
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Medicina is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 1800 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • molecular medicine
  • medical genetics
  • genomics
  • precision medicine
  • clinical practice

Published Papers (1 paper)

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Research

14 pages, 1994 KiB  
Article
Olmutinib Reverses Thioacetamide-Induced Cell Cycle Gene Alterations in Mice Liver and Kidney Tissues, While Wheat Germ Treatment Exhibits Limited Efficacy at Gene Level
by Seema Zargar, Tanveer A. Wani, Salman Alamery and Fatimah Yaseen
Medicina 2024, 60(4), 639; https://doi.org/10.3390/medicina60040639 - 16 Apr 2024
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Abstract
Background and Objectives: TAA is potent hepatic/renal toxicant. Conversely, WGO is a potent dietary supplement with impressive antioxidant properties. Olmutinib is an apoptotic chemotherapy drug that does not harm the liver or kidney. This study investigated the impact of olmutinib and wheat [...] Read more.
Background and Objectives: TAA is potent hepatic/renal toxicant. Conversely, WGO is a potent dietary supplement with impressive antioxidant properties. Olmutinib is an apoptotic chemotherapy drug that does not harm the liver or kidney. This study investigated the impact of olmutinib and wheat germ oil (WGO) on Thioacetamide (TAA)-induced gene alterations in mice liver and kidney tissues. Materials and Methods: Adult male C57BL/6 mice were exposed to 0.3% TAA in drinking water for 14 days, followed by the oral administration of olmutinib (30 mg/kg) and WGO (1400 mg/kg) for 5 consecutive days. Treatment groups included the following: groups I (control), II (TAA-exposed), III (TAA + olmutinib), IV (TAA + WGO), and V (TAA + olmutinib + WGO). Results: The findings revealed that TAA exposure increased MKi67 and CDKN3 gene expression in liver and kidney tissues. Olmutinib treatment effectively reversed these TAA-induced effects, significantly restoring MKi67 and CDKN3 gene expression. WGO also reversed MKi67 effects in the liver but exhibited limited efficacy in reversing CDKN3 gene alterations induced by TAA exposures in both the liver and kidney. TAA exposure showed the tissue-specific expression of TP53, with decreased expression in the liver and increased expression in the kidney. Olmutinib effectively reversed these tissue-specific alterations in TP53 expression. While WGO treatment alone could not reverse the gene alterations induced by TAA exposure, the co-administration of olmutinib and WGO exhibited a remarkable potentiation of therapeutic effects in both the liver and kidney. The gene interaction analysis revealed 77.4% of physical interactions and co-localization between MKi67, CDKN3, and TP53 expressions. Protein–protein interaction networks also demonstrated physical interactions between MKi67, TP53, and CDKN3, forming complexes or signaling cascades. Conclusions: It was predicted that the increased expression of the MKi67 gene by TAA leads to the increase in TP53, which negatively regulates the cell cycle via increased CDKN3 expression in kidneys and the restoration of TP53 levels in the liver. These findings contribute to our understanding of the effects of olmutinib and WGO on TAA-induced gene expression changes and highlight their contrasting effects based on cell cycle alterations. Full article
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Planned Papers

The below list represents only planned manuscripts. Some of these manuscripts have not been received by the Editorial Office yet. Papers submitted to MDPI journals are subject to peer-review.

Title: Primary lymphoma of the bone
Authors: Jasminka Talapko
Affiliation: Faculty of Medicine and Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia
Abstract: /

Title: Targeted therapy in non-small cell lung cancer
Authors: Ivan Alerić
Affiliation: Faculty of Medicine and Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia
Abstract: /

Title: Molecular diagnostic in lyposarcoma
Authors: Ivana Škrlec
Affiliation: Faculty of Medicine and Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia
Abstract: /

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