Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Doxorubicin and Cisplatin Modulate miR-21, miR-106, miR-126, miR-155 and miR-199 Levels in MCF7, MDA-MB-231 and SK-BR-3 Cells That Makes Them Potential Elements of the DNA-Damaging Drug Treatment Response Monitoring in Breast Cancer Cells—A Preliminary Study
by
Lisiak, Natalia
, Mizielska, Anna
, Szczepański, Radosław
, Ślężak, Jan
, Kopczyński, Przemysław
, Rymarczyk, Marta
, Dąbrowska, Małgorzata
, Dziechciowska, Iga
, Cisek, Małgorzata
, Totoń, Ewa
, Kosmalska, Izabela
, Rubiś, Błażej
, Wilkowska, Klaudia
, Jacczak, Barbara
in
Angiogenesis
/ Apoptosis
/ Biomarkers
/ Breast cancer
/ breast neoplasms
/ Breast Neoplasms - drug therapy
/ Breast Neoplasms - genetics
/ Breast Neoplasms - metabolism
/ Cancer
/ Cancer cells
/ Cancer therapies
/ cell lines
/ Cells
/ Chemotherapy
/ Cisplatin
/ Cisplatin - pharmacology
/ DNA
/ DNA damage
/ DNA repair
/ Doxorubicin
/ Doxorubicin - pharmacology
/ Drug therapy
/ Drugs
/ Epigenetics
/ Female
/ Gene amplification
/ Genetic aspects
/ Humans
/ MCF-7 Cells
/ Medical innovations
/ Metabolism
/ Metastasis
/ MicroRNA
/ MicroRNAs
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ miRNA
/ neoplasm cells
/ Oncology, Experimental
/ Pharmacovigilance
/ Product safety
/ Tumor cell lines
2023
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Doxorubicin and Cisplatin Modulate miR-21, miR-106, miR-126, miR-155 and miR-199 Levels in MCF7, MDA-MB-231 and SK-BR-3 Cells That Makes Them Potential Elements of the DNA-Damaging Drug Treatment Response Monitoring in Breast Cancer Cells—A Preliminary Study
by
Lisiak, Natalia
, Mizielska, Anna
, Szczepański, Radosław
, Ślężak, Jan
, Kopczyński, Przemysław
, Rymarczyk, Marta
, Dąbrowska, Małgorzata
, Dziechciowska, Iga
, Cisek, Małgorzata
, Totoń, Ewa
, Kosmalska, Izabela
, Rubiś, Błażej
, Wilkowska, Klaudia
, Jacczak, Barbara
in
Angiogenesis
/ Apoptosis
/ Biomarkers
/ Breast cancer
/ breast neoplasms
/ Breast Neoplasms - drug therapy
/ Breast Neoplasms - genetics
/ Breast Neoplasms - metabolism
/ Cancer
/ Cancer cells
/ Cancer therapies
/ cell lines
/ Cells
/ Chemotherapy
/ Cisplatin
/ Cisplatin - pharmacology
/ DNA
/ DNA damage
/ DNA repair
/ Doxorubicin
/ Doxorubicin - pharmacology
/ Drug therapy
/ Drugs
/ Epigenetics
/ Female
/ Gene amplification
/ Genetic aspects
/ Humans
/ MCF-7 Cells
/ Medical innovations
/ Metabolism
/ Metastasis
/ MicroRNA
/ MicroRNAs
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ miRNA
/ neoplasm cells
/ Oncology, Experimental
/ Pharmacovigilance
/ Product safety
/ Tumor cell lines
2023
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Doxorubicin and Cisplatin Modulate miR-21, miR-106, miR-126, miR-155 and miR-199 Levels in MCF7, MDA-MB-231 and SK-BR-3 Cells That Makes Them Potential Elements of the DNA-Damaging Drug Treatment Response Monitoring in Breast Cancer Cells—A Preliminary Study
by
Lisiak, Natalia
, Mizielska, Anna
, Szczepański, Radosław
, Ślężak, Jan
, Kopczyński, Przemysław
, Rymarczyk, Marta
, Dąbrowska, Małgorzata
, Dziechciowska, Iga
, Cisek, Małgorzata
, Totoń, Ewa
, Kosmalska, Izabela
, Rubiś, Błażej
, Wilkowska, Klaudia
, Jacczak, Barbara
in
Angiogenesis
/ Apoptosis
/ Biomarkers
/ Breast cancer
/ breast neoplasms
/ Breast Neoplasms - drug therapy
/ Breast Neoplasms - genetics
/ Breast Neoplasms - metabolism
/ Cancer
/ Cancer cells
/ Cancer therapies
/ cell lines
/ Cells
/ Chemotherapy
/ Cisplatin
/ Cisplatin - pharmacology
/ DNA
/ DNA damage
/ DNA repair
/ Doxorubicin
/ Doxorubicin - pharmacology
/ Drug therapy
/ Drugs
/ Epigenetics
/ Female
/ Gene amplification
/ Genetic aspects
/ Humans
/ MCF-7 Cells
/ Medical innovations
/ Metabolism
/ Metastasis
/ MicroRNA
/ MicroRNAs
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ miRNA
/ neoplasm cells
/ Oncology, Experimental
/ Pharmacovigilance
/ Product safety
/ Tumor cell lines
2023
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Doxorubicin and Cisplatin Modulate miR-21, miR-106, miR-126, miR-155 and miR-199 Levels in MCF7, MDA-MB-231 and SK-BR-3 Cells That Makes Them Potential Elements of the DNA-Damaging Drug Treatment Response Monitoring in Breast Cancer Cells—A Preliminary Study
Journal Article
Doxorubicin and Cisplatin Modulate miR-21, miR-106, miR-126, miR-155 and miR-199 Levels in MCF7, MDA-MB-231 and SK-BR-3 Cells That Makes Them Potential Elements of the DNA-Damaging Drug Treatment Response Monitoring in Breast Cancer Cells—A Preliminary Study
2023
Request Book From Autostore
and Choose the Collection Method
Overview
One of the most innovative medical trends is personalized therapy, based on simple and reproducible methods that detect unique features of cancer cells. One of the good prognostic and diagnostic markers may be the miRNA family. Our work aimed to evaluate changes in selected miRNA levels in various breast cancer cell lines (MCF7, MDA-MB-231, SK-BR-3) treated with doxorubicin or cisplatin. The selection was based on literature data regarding the most commonly altered miRNAs in breast cancer (21-3p, 21-5p, 106a-5p, 126-3p, 126-5p, 155-3p, 155-5p, 199b-3p, 199b-5p, 335-3p, 335-5p). qPCR assessment revealed significant differences in the basal levels of some miRNAs in respective cell lines, with the most striking difference in miR-106a-5p, miR-335-5p and miR-335-3p—all of them were lowest in MCF7, while miR-153p was not detected in SK-BR-3. Additionally, different alterations of selected miRNAs were observed depending on the cell line and the drug. However, regardless of these variables, 21-3p/-5p, 106a, 126-3p, 155-3p and 199b-3p miRNAs were shown to respond either to doxorubicin or to cisplatin treatment. These miRNAs seem to be good candidates for markers of breast cancer cell response to doxorubicin or cisplatin. Especially since some earlier reports suggested their role in affecting pathways and expression of genes associated with the DNA-damage response. However, it must be emphasized that the preliminary study shows effects that may be highly related to the applied drug itself and its concentration. Thus, further examination, including human samples, is required.
Publisher
MDPI AG,MDPI
Subject
/ Breast Neoplasms - drug therapy
/ Breast Neoplasms - metabolism
/ Cancer
/ Cells
/ DNA
/ Drugs
/ Female
/ Humans
/ MicroRNA
/ miRNA
MBRLCatalogueRelatedBooks
Related Items
Related Items
We currently cannot retrieve any items related to this title. Kindly check back at a later time.
This website uses cookies to ensure you get the best experience on our website.