Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Goldoost, Solmaza | Zarredar, Habibb | Asadi, Miladc | Shirvaliloo, Miladd; e | Raeisi, Mortazaf;
Affiliations: [a] Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran | [b] Tuberculosis and Lung Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran | [c] Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran | [d] Future Science Group, London, UK | [e] Infectious and Tropical Diseases Research Center, Tabriz University of Medical Sciences, Tabriz, Iran | [f] Hematology and Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
Correspondence: [*] Corresponding author: Mortaza Raeisi, Hematology and Oncology Research Center, Tabriz University of Medical Sciences, 15731 Tabriz, Iran. E-mail: raiisy@yahoo.com, raeisim@tbzmed.ac.ir. ORCIDs: https://orcid.org/0000-0002-3173-1610
Abstract: AIM:In the present study, we sought to explore potential differences in the expression and promoter methylation of mitogen-activated protein kinase 1 (MAPK1) between tumor and marginal cells of breast cancer lesions. METHODS:A total of 50 randomly selected patients with breast cancer (BCa) undergoing needle biopsy were enrolled. Clinical specimens containing both tumor and marginal cells were collected and preserved. After DNA extraction using specific primers, MAPK1 mRNA and promoter methylation were measured with spectrophotometry at 260/280 nm absorption wavelengths. To deliver a comparative analysis, data from The Cancer Genome Atlas (TCGA) program regarding breast cancer (BRCA), were downloaded from Xena Functional Genomics Explorer and separately analyzed. The suitability of MAPK1 expression and promoter methylation as biomarkers for BCa was analyzed with receiver operating characteristic (ROC) curves. RESULTS:We found a positive correlation between tumor stage and MAPK1 expression (P-value: 0.029) in BCa. Likewise, MAPK1 expression was significantly associated with lymph node metastasis (P-value: 0.018). There was a significant difference in the expression of MAPK1 mRNA between tumor and marginal cells of BCa and BRCA (P-value < 0.001). However, we did not find any statistically significant difference in MAPK1 promoter methylation between tumor and marginal cells of both BCa and BRCA. With an area under the curve (AUC) of 0.71, the diagnostic accuracy of MAPK1 expression in BCa and BRCA was validated. However, MAPK1 promoter methylation was not found to be a suitable biomarker. CONCLUSION:Our findings suggest that while MAPK1 expression, might be a promising biomarker for evaluating oncogenic activity in patients suspected of BCa. We were not able to detect a prognostic/diagnostic role for MAPK1 promoter methylation.
Keywords: Breast cancer, mitogen-activated protein kinase 1, MAPK1, ERK2, promoter methylation
DOI: 10.3233/BD-230001
Journal: Breast Disease, vol. 42, no. 1, pp. 437-445, 2023
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
sales@iospress.com
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
info@iospress.nl
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office info@iospress.nl
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
china@iospress.cn
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
如果您在出版方面需要帮助或有任何建, 件至: editorial@iospress.nl