Joanna Olejnik-Wojciechowska

Mrs. Joanna Olejnik-Wojciechowska

orcid

Research Focus & Metrics

Academic Career Length

4Years (2023-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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EBEstera Bakinowska
Estera Bakinowska
JOJoanna Olejnik-Wojciechowska
Joanna Olejnik-Wojciechowska
KKKajetan Kiełbowski
Kajetan Kiełbowski
ASAnastasiia Skoryk
Anastasiia Skoryk
APAndrzej Pawlik
Andrzej Pawlik
Chronic kidney disease (CKD) is a progressive disorder associated with a decline in kidney function. Consequently, patients with advanced stages of CKD require renal replacement therapies, such as dialysis and kidney transplantation. Various conditions lead to the development of CKD, including diabetes mellitus, hypertension, and glomerulonephritis, among others. The disease is associated with metabolic and hormonal dysregulation, including uraemia and hyperparathyroidism, as well as with low-grade systemic inflammation. Altered homeostasis increases the risk of developing severe comorbidities, such as cardiovascular diseases or sarcopenia, which increase mortality. Sarcopenia is defined as a progressive decline in muscle mass and function. However, the precise mechanisms that link CKD and the development of sarcopenia are poorly understood. Knowledge about these linking mechanisms might lead to the introduction of precise treatment strategies that could prevent muscle wasting. This review discusses inflammatory mediators, metabolic and hormonal dysregulation, gut microbiota dysbiosis, and non-coding RNA alterations that could link CKD and sarcopenia.

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JOJoanna Olejnik-Wojciechowska
Joanna Olejnik-Wojciechowska
DBDominika Boboryko
Dominika Boboryko
Aleksandra Wiktoria BratborskaAleksandra Wiktoria Bratborska
Aleksandra Wiktoria Bratborska
KRKlaudia Rusińska
Klaudia Rusińska
POPiotr Ostrowski
Piotr Ostrowski
APAndrzej Pawlik
Andrzej Pawlik
Psoriasis is a chronic inflammatory skin disease, the prevalence of which is increasing. Genetic, genomic, and epigenetic changes play a significant role in the pathogenesis of psoriasis. This review summarizes the impact of epigenetics on the development of psoriasis and highlights challenges for the future. The development of epigenetics provides a basis for the search for genetic markers associated with the major histocompatibility complex. Genome-wide association studies have made it possible to link psoriasis to genes and therefore to epigenetics. The acquired knowledge may in the future serve as a solid foundation for developing newer, increasingly effective methods of treating psoriasis. In this narrative review, we discuss the role of epigenetic factors in the pathogenesis of psoriasis.

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EBEstera Bakinowska
Estera Bakinowska
KKKajetan Kiełbowski
Kajetan Kiełbowski
DBDominika Boboryko
Dominika Boboryko
Aleksandra Wiktoria BratborskaAleksandra Wiktoria Bratborska
Aleksandra Wiktoria Bratborska
JOJoanna Olejnik-Wojciechowska
Joanna Olejnik-Wojciechowska
APAndrzej Pawlik
Andrzej Pawlik
Cardiovascular diseases (CVDs) are the leading cause of death and include several vascular and cardiac disorders, such as atherosclerosis, coronary artery disease, cardiomyopathies, and heart failure. Multiple treatment strategies exist for CVDs, but there is a need for regenerative treatment of damaged heart. Stem cells are a broad variety of cells with a great differentiation potential that have regenerative and immunomodulatory properties. Multiple studies have evaluated the efficacy of stem cells in CVDs, such as mesenchymal stem cells and induced pluripotent stem cell-derived cardiomyocytes. These studies have demonstrated that stem cells can improve the left ventricle ejection fraction, reduce fibrosis, and decrease infarct size. Other studies have investigated potential methods to improve the survival, engraftment, and functionality of stem cells in the treatment of CVDs. The aim of the present review is to summarize the current evidence on the role of stem cells in the treatment of CVDs, and how to improve their efficacy.

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EBEstera Bakinowska
Estera Bakinowska
KKKajetan Kiełbowski
Kajetan Kiełbowski
PSPatryk Skorka
Patryk Skorka
ADAleksandra Dach
Aleksandra Dach
JOJoanna Olejnik-Wojciechowska
Joanna Olejnik-Wojciechowska
APAndrzej Pawlik
Andrzej Pawlik
Non-coding RNAs (ncRNAs) represent a broad family of molecules that regulate gene expression, including microRNAs, long non-coding RNAs and circular RNAs, amongst others. Dysregulated expression of ncRNAs alters gene expression, which is implicated in the pathogenesis of several malignancies and inflammatory diseases. Gastric cancer is the fifth most frequently diagnosed cancer and the fourth most common cause of cancer-related death. Studies have found that altered expression of ncRNAs may contribute to tumourigenesis through regulating proliferation, apoptosis, drug resistance and metastasis. This review describes the potential use of ncRNAs as diagnostic and prognostic biomarkers. Moreover, we discuss the involvement of ncRNAs in the pathogenesis of gastric cancer, including their interactions with the members of major signalling pathways.

24 October 2023 in Journal of Clinical Medicine
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MMMonika Marzanna Modrzejewska
Monika Marzanna Modrzejewska
JOJoanna Olejnik-Wojciechowska
Joanna Olejnik-Wojciechowska
ARAgnieszka Roszyk
Agnieszka Roszyk
ESElwira Szychot
Elwira Szychot
TKTomasz Dariusz Konczak
Tomasz Dariusz Konczak
JPJarosław Władysław Peregud-Pogorzelski
Jarosław Władysław Peregud-Pogorzelski
In this paper, the authors present a clinical picture of the diagnosis and current treatment regimens of optic pathway glioma in the pediatric population, with an emphasis on the role of an ophthalmic diagnosis in the differentiation and monitoring of lesions. Glioma is the most common optic nerve tumor in children. Material: Articles in PubMed, Scholar and Website were reviewed, taking into account current standards of management related to sporadic or NF1-related optic glioma, epidemiology, location, course of the disease, clinical manifestations, histological types of the tumor, genetic predisposition, diagnostic ophthalmic tests currently applicable in therapeutic monitoring of the tumor, neurological diagnosis, therapeutic management and prognosis. The importance of current screening recommendations, in line with standards, was emphasized. Results: Glioma occurs in children most often in the first decade of life. Initially, they may be asymptomatic, and clinically ophthalmic changes are associated with the organ of vision or with systemic changes. Gliomas associated with the NF1 mutation have a better prognosis for sporadic gliomas. Diagnosis includes radiological imaging methods/MRI/ophthalmology/OCT and visual acuity log MAR assessment. The basis of treatment is clinical observation. In the case of disease progression, surgical treatment, chemotherapy and targeted therapy are used. Conclusion: Further research into novel techniques for detecting gliomas would allow for early monitoring of the disease.

10 August 2024 in Biomolecules
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JŻJustyna Żychowska
Justyna Żychowska
MĆMaciej Ćmil
Maciej Ćmil
PSPatryk Skorka
Patryk Skorka
JOJoanna Olejnik-Wojciechowska
Joanna Olejnik-Wojciechowska
PPPaulina Plewa
Paulina Plewa
APAndrzej Pawlik
Andrzej Pawlik
Hepatitis C virus (HCV) is a hepatotropic virus that can be transmitted through unsafe medical procedures, such as injections, transfusions, and dental treatment. The infection may be self-limiting or manifest as a chronic form that induces liver fibrosis, cirrhosis, or progression into hepatocellular carcinoma (HCC). Epigenetic mechanisms are major regulators of gene expression. These mechanisms involve DNA methylation, histone modifications, and the activity of non-coding RNAs, which can enhance or suppress gene expression. Abnormal activity or the dysregulated expression of epigenetic molecules plays an important role in the pathogenesis of various pathological disorders, including inflammatory diseases and malignancies. In this review, we summarise the current evidence on epigenetic mechanisms involved in HCV infection and progression to HCC.