TWIST1 GENE EXPRESSION AS A BIOMARKER FOR PREDICTING PRIMARY DOXORUBICIN RESISTANCE IN BREAST
Staninova-Stojovska M1, Matevska-Geskovska N1, Panovski M2, Angelovska B3, Mitrevski N3, Ristevski M3, Jovanovic R4, Dimovski AJ1,5,
*Corresponding Author: Professor Aleksandar J. Dimovski, M.D., Ph.D., Center for Biomolecular Pharmaceutical Analyses, UKIM Faculty of Pharmacy, Majka Tereza 47, and Research Center for Genetic Engineering and Biotechnology, Macedonian Academy of Sciences and Arts, Krste Misirkov 2, 1000 Skopje, RN Macedonia. Tel/Fax: +389-2-3235411. E-mail: adimovski@ff.ukim.edu.mk
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INTRODUCTION

Breast cancer is the most common cancer in women and is also responsible for a great number of cancer-associated deaths among women worldwide [1,2]. Several chemo-therapeutic agents, either alone or in addition to other therapies, are used in the treatment of breast cancer patients. Anthracyclines and taxanes are the most commonly used chemo-therapeutics for breast cancer treatment [3]. Benefit and risk assessment for therapeutic agents for each patient is important because chemotherapy is a conventional method targeting all fast-dividing cells of the organism [4]. Toxicity and primary or secondary resistance are common problems of conventional chemotherapy. Thus, studies focusing on finding biomarkers to predict the response of the patients and tumors to the drugs used are an important part of precision medicine [5]. The twist transcription factor, encoded by the TWIST1 gene (TWIST1; OMIM* 601622) is a member of the basic helix loop helix transcription factor family and has an



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