Agnieszka Klupczynska-Gabryszak

Dr. Agnieszka Klupczynska-Gabryszak

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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1 January 2017 in International Journal of Medical Sciences
Verified
Journal Article
Open access
PDPaweł Dereziński
Paweł Dereziński
AKAgnieszka Klupczynska-Gabryszak
Agnieszka Klupczynska-Gabryszak
WSWojciech Sawicki
Wojciech Sawicki
JPJerzy Palka
Jerzy Palka
ZKZenon J. Kokot
Zenon J. Kokot
There is a great interest in searching for diagnostic biomarkers in prostate cancer patients. The aim of the pilot study was to evaluate free amino acid profiles in their serum and urine. The presented paper shows the first comprehensive analysis of a wide panel of amino acids in two different physiological fluids obtained from the same groups of prostate cancer patients (n = 49) and healthy men (n = 40). The potential of free amino acids, both proteinogenic and non-proteinogenic, as prostate cancer biomarkers and their utility in classification of study participants have been assessed. Several metabolites, which deserve special attention in the further metabolomic investigations on searching for prostate cancer markers, were indicated. Moreover, free amino acid profiles enabled to classify samples to one of the studied groups with high sensitivity and specificity. The presented research provides a strong evidence that ethanolamine, arginine and branched-chain amino acids metabolic pathways can be a valuable source of markers for prostate cancer. The altered concentrations of the above-mentioned metabolites suggest their role in pathogenesis of prostate cancer and they should be further evaluated as clinically useful markers of prostate cancer.

17 March 2020 in Scientific Reports
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Journal Article
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ASAnna Sulej-Suchomska
Anna Sulej-Suchomska
AKAgnieszka Klupczynska-Gabryszak
Agnieszka Klupczynska-Gabryszak
PDPaweł Dereziński
Paweł Dereziński
JMJan Matysiak
Jan Matysiak
PPPiotr Przybyłowski
Piotr Przybyłowski
ZKZenon J. Kokot
Zenon J. Kokot
The use of illicit drugs causes unquestionable societal and economic damage. To implement actions aimed at combating drug abuse, it is necessary to assess illicit drug consumption patterns. The purpose of this paper was to develop, optimize, validate and apply a procedure for determining new psychoactive substances (NPSs) and classic drugs of abuse and their main metabolites in wastewater samples by using solid phase extraction (SPE) and high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS). Moreover, detailed validation of the procedure was conducted. The developed SPE–HPLC-MS/MS procedure (within the sewage-based epidemiology strategy) allowed for the simultaneous, selective, very sensitive, accurate (recoveries ≥ 80.1%) and precise (CV ≤ 8.1%) determination of new and classic psychoactive substances in wastewater samples. This study is characterized by new scientific elements, especially in terms of the freeze-thaw and post-preparative stability of the selected psychoactive substances. This is the first time that NPSs (mephedrone and ketamine), the main metabolites of heroin (6-acetylmorphine, 6-AM) and marijuana (11-nor-9-carboxy-Δ9-tetrahydrocannabinol, THC-COOH) have been detected and monitored in Poland. This study is also the first to corroborate the data available from the EMCDDA and EUROPOL report and indicates that the retail market for cocaine is expanding in Eastern Europe.

1 October 2016 in Lung Cancer
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Journal Article
Closed access
AKAgnieszka Klupczynska-Gabryszak
Agnieszka Klupczynska-Gabryszak
PDPaweł Dereziński
Paweł Dereziński
WDWojciech Dyszkiewicz
Wojciech Dyszkiewicz
KPKrystian Pawlak
Krystian Pawlak
MKMariusz Kasprzyk
Mariusz Kasprzyk
ZKZenon J. Kokot
Zenon J. Kokot

21 April 2021 in Molecules
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Journal Article
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EMEliza Matuszewska-Mach
Eliza Matuszewska-Mach
AKAgnieszka Klupczynska-Gabryszak
Agnieszka Klupczynska-Gabryszak
KMKrzysztof Maciołek
Krzysztof Maciołek
ZKZenon J. Kokot
Zenon J. Kokot
JMJan Matysiak
Jan Matysiak
Beehive products possess nutritional value and health-promoting properties and are recommended as so-called “superfoods”. However, because of their natural origin, they may contain relevant elemental contaminants. Therefore, to assess the quality of bee products, we examined concentrations of a broad range of 24 selected elements in propolis, bee pollen, and royal jelly. The quantitative analyses were performed with inductively coupled plasma-mass spectrometry (ICP-MS) and inductively coupled plasma optical emission spectrometry (ICP-OES) techniques. The results of our research indicate that bee products contain essential macronutrients (i.e., K, P, and S) and micronutrients (i.e., Zn and Fe) in concentrations depending on the products’ type. However, the presence of toxic heavy metals makes it necessary to test the quality of bee products before using them as dietary supplements. Bearing in mind that bee products are highly heterogenous and, depending on the environmental factors, differ in their elemental content, it is necessary to develop standards regulating the acceptable levels of inorganic pollutants. Furthermore, since bees and their products are considered to be an effective biomonitoring tool, our results may reflect the environment’s condition in west-central Poland, affecting the health and well-being of both humans and bees.

6 February 2017 in Journal of Cancer Research and Clinical Oncology
Verified
Journal Article
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AKAgnieszka Klupczynska-Gabryszak
Agnieszka Klupczynska-Gabryszak
PDPaweł Dereziński
Paweł Dereziński
TGTimothy J. Garrett
Timothy J. Garrett
VRVanessa Y. Rubio
Vanessa Y. Rubio
WDWojciech Dyszkiewicz
Wojciech Dyszkiewicz
ZKZenon J. Kokot
Zenon J. Kokot
Purpose The aim of the project was to apply ultra-high-performance liquid chromatography–quadrupole-Orbitrap-high-resolution mass spectrometry for serum metabolite profiling of non-small-cell lung cancer (NSCLC). This Orbitrap-based methodology has been applied for a study of NSCLC potential markers for the first time. Methods After extraction using protein precipitation, sera were separated on the ACE Excel 2 C18-PFP (100 × 2.1 mm, 2.0 µm) column using gradient elution and analyzed within the range of 70–1000 m/z. Only patients with early stage disease (stages IA–IIB) were included in the study, providing opportunity to find biomarkers for early lung cancer detection. The resulting metabolite profiles were subjected to univariate and multivariate statistical tests. Results 36 features were found significantly changed between NSCLC group and controls after FDR adjustment and 19 were identified using various metabolite databases (in-house library, HMDB, mzCloud). The study revealed a number of NSCLC biomarker candidates which belong to such compound classes as acylcarnitines, organic acids, and amino acids. Multivariate ROC curve built using 12 identified metabolites was characterized by AUC = 0.836 (0.722–0.946). There were no significant differences in the serum metabolite profiles between two most common histological types of lung cancer—adenocarcinoma and squamous cell carcinoma. Conclusions Through identification of novel potential tumor markers, Orbitrap-based global metabolic profiling is a useful strategy in cancer research. Our study can accelerate development of new diagnostic and therapeutic strategies in NSCLC. The metabolites involved in discrimination between NSCLC patients and the control subjects should be further explored using a targeted approach.

Verified
Journal Article
Open access
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SPSzymon Plewa
Szymon Plewa
AHAgnieszka Horała
Agnieszka Horała
PDPaweł Dereziński
Paweł Dereziński
AKAgnieszka Klupczynska-Gabryszak
Agnieszka Klupczynska-Gabryszak
ENEwa Nowak-Markwitz
Ewa Nowak-Markwitz
ZKZenon J. Kokot
Zenon J. Kokot
The aim of this study was to quantitate 42 serum-free amino acids, propose the biochemical explanation of their role in tumor development, and identify new ovarian cancer (OC) biomarkers for potential use in OC screening. The additional value of this work is the schematic presentation of the interrelationship between metabolites which were identified as significant for OC development and progression. The liquid chromatography-tandem mass spectrometry technique using highly-selective multiple reaction monitoring mode and labeled internal standards for each analyzed compound was applied. Performed statistical analyses showed that amino acids are potentially useful as OC biomarkers, especially as variables in multi-marker models. For the distinguishing metabolites the following metabolic pathways involved in cancer growth and development were proposed: histidine metabolism; tryptophan metabolism; arginine biosynthesis; arginine and proline metabolism; and alanine, aspartate and glutamine metabolism. The presented research identifies histidine and citrulline as potential new OC biomarkers. Furthermore, it provides evidence that amino acids are involved in metabolic pathways related to tumor growth and play an important role in cancerogenesis.