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: Sadeghi, Minoosha | Gholizadeh, Majidb | Safataj, Nedac; d | Tahmasebivand, Mahsae | Mohajeri, Gholamrezaf | Lotfi, Hajieg | Bostanabad, Saber Yarih | Safar, Behnaza; | Salehi, Mansoori; j;
Affiliations: [a] Department of Genetics, Faculty of Science, Shahrekord University, Shahrekord, Iran | [b] Department of Hematology and Blood Banking, Faculty of Allied Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran | [c] Department of Genetics, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran | [d] Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran | [e] Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran | [f] Department of Surgery, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran | [g] Cellular and Molecular Research Center, Research Institute for Prevention of Non-Communicable Disease, Qazvin University of Medical Sciences, Qazvin, Iran | [h] Department of Pharmacology, Faculty of Pharmacy, Istanbul Health and Technology University, Istanbul, Turkey | [i] Cellular, Molecular and Genetics Research Center, Isfahan University of Medical Sciences, Isfahan, Iran | [j] Medical Genetics Research Center of Genome, Isfahan University of Medical Sciences, Isfahan, Iran
Correspondence: [*] Corresponding authors: Dr. Behnaz Safar, Department of Genetics, Faculty of Science, Shahrekord University, Shahrekord, Iran. Tel.: +98 3832324419; E-mail: saffar_b@sci.sku.ac.ir and Dr. Mansoor Salehi, Cellular, Molecular, and Genetics Research Center, Isfahan University of Medical Sciences, Isfahan 8175954319, Iran and Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan 8175954319, Iran. Tel.: +98 3136246922; Fax: +98 3136258320; E-mail: m_salehi@med.mui.ac.ir, genome.res.cent@gmail.com
Abstract: BACKGROUND:Breast cancer (BC) is the most prevalent cancer in women, with increasing incidence and death rates in recent years. Disruptions of different signaling pathways partially cause breast cancer. Hence, different genes through particular pathways are involved in BC tumorigenesis. METHODS:In this study, we evaluated the expression level of GLIS2 and CCND1 genes in 50 patients. Also, in-silico analyses were used to enrich related signaling pathways involving the mentioned genes. RESULTS:The results showed an increased expression level of Cyclin D1 and decreased expression level of GLIS2 in BC patients. Moreover, a relationship between aberrant expression levels of GLIS2 and CCND1 and BC development was determined. CONCLUSION:These observations could help uncover new therapeutic targets for treating patients with BC in the progressive stage.
Keywords: Breast cancer, GLIS2 , CCND1 , signaling pathway
DOI: 10.3233/BD-220068
Journal: Breast Disease, vol. 42, no. 1, pp. 251-259, 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