TY  - JOUR
T1  - DETERMINATION OF THE THERAPEUTIC EFFECT OF VULPINIC ACID AND VULPINIC ACID-RESPONSIVE miR-197-3P IN BREAST CANCER TREATMENT BY IN VITRO AND IN VIVO STUDIES
TT  - DETERMINATION OF THE THERAPEUTIC EFFECT OF VULPINIC ACID AND VULPINIC ACID-RESPONSIVE miR-197-3P IN BREAST CANCER TREATMENT BY IN VITRO AND IN VIVO STUDIES
AU  - Cansaran Duman, Doç. Dr. Demet
PY  - 2022
DA  - August
DO  - 10.26650/JARHS2021-1136842
JF  - Journal of Advanced Research in Health Sciences
JO  - SABİAD
PB  - Istanbul University
WT  - DergiPark
SN  - 2651-4060
SP  - 26
EP  - 26
VL  - 5
IS  - S-1
LA  - tr
AB  - Breast cancer is the most common type of cancer in women and an effective treatment method has not been developed yet. Researchers are working onalternative treatment options that do not have toxic side effects based on the patient’s resistance to chemotherapeutics over time. Our study revealedmolecular characterization and in vivo experimental studies of vulpinic acid and vulpinic acid-responsive miRNAs on breast cancer. miRNAs formed by theapplication of vulpinic acid on breast cancer and normal cells were determined by microarray analysis. The genes and pathway analyses targeted bymiRNAs were determined using bioinformatics tools. As a result of the bioinformatic analysis, it was determined that miR-197-3p was associated withbreast cancer. The anti-proliferative activity of miR-197-3p responsive to vulpinic acid was determined in MCF-7 breast cancer and MCF-12A cells. Peptideidentification was performed to evaluate the effect of vulpinic acid-responsive miR-197-3p at the proteome level, and the relationship between targetproteins was determined using bioinformatics tools. A xenograft breast cancer model was used to understand the in vivo effects of vulpinic acid and miR-197-3p on breast cancer. The obtained results revealed the effect of vulpinic acid-responsive miR-197-3p on the development of breast cancer andstrengthened the possibility of an alternative treatment method in the future. With the data obtained, the effect of vulpinic acid-responsive miR-197-3pin breast cancer treatment was determined for the first time and presented to the literature and the pharmaceutical industry as an effective, reliable, andcost-effective treatment approach.
KW  - Vulpinic acid
KW  - Drug Candidate Molecule
KW  - miR-197-3p
N2  - Breast cancer is the most common type of cancer in women and an effective treatment method has not been developed yet. Researchers are working on alternative treatment options that do not have toxic side effects based on the patient’s resistance to chemotherapeutics over time. Our study revealed molecular characterization and in vivo experimental studies of vulpinic acid and vulpinic acid-responsive miRNAs on breast cancer. miRNAs formed by the application of vulpinic acid on breast cancer and normal cells were determined by microarray analysis. The genes and pathway analyses targeted by miRNAs were determined using bioinformatics tools. As a result of the bioinformatic analysis, it was determined that miR-197-3p was associated with breast cancer. The anti-proliferative activity of miR-197-3p responsive to vulpinic acid was determined in MCF-7 breast cancer and MCF-12A cells. Peptide identification was performed to evaluate the effect of vulpinic acid-responsive miR-197-3p at the proteome level, and the relationship between target proteins was determined using bioinformatics tools. A xenograft breast cancer model was used to understand the in vivo effects of vulpinic acid and miR- 197-3p on breast cancer. The obtained results revealed the effect of vulpinic acid-responsive miR-197-3p on the development of breast cancer and strengthened the possibility of an alternative treatment method in the future. With the data obtained, the effect of vulpinic acid-responsive miR-197-3p in breast cancer treatment was determined for the first time and presented to the literature and the pharmaceutical industry as an effective, reliable, and cost-effective treatment approach.
CR  - Grozescu T, Popa F. Prostate cancer between prognosis and adequate/proper therapy. J Med Life. 2017;10(1):5-12
UR  - https://doi.org/10.26650/JARHS2021-1136842
L1  - https://dergipark.org.tr/en/download/article-file/2511367
ER  -