Maryam Rahimi - Department of Microbiology, Karaj Branch, Islamic Azad University, Karaj, Iran
Setareh Talebi Kakroodi - Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
Mansoureh Tajvidi - Clinical care and Health Promotion Research Center, Karaj Branch, Islamic Azad University, Karaj, Iran

Receptor tyrosine kinase (RTK) signaling is a crucial pathway in the development of many cancers. KIT, PI۳K, and AKT are the major genes in this pathway. KIT RTK functions in cell signal transduction in various cell types, such as cancer cells. A central element of RTK signaling is phosphatidylinositol-۴, ۵-bisphosphate ۳-kinase catalytic subunit A (PIK۳CA), involved in cell proliferation, survival, and growth. AKT is a serine/threonine-specific protein kinase that has an important role in several processes, such as apoptosis and cell proliferation. The importance of mutations and overexpression of KIT, PI۳K, and AKT genes in breast cancer has been previously demonstrated. This review investigated the relationship between gene mutations and overexpression and clinicopathological variable of KIT, PI۳K, and AKT in breast cancer. Finally, the role of inhibitor drugs of these genes in breast cancer treatment. These data were collected from PubMed and Google Scholar databases from ۲۰۰۰ to ۲۰۲۱. The expression of KIT, PI۳K, and AKT genes in normal breast tissues has been observed. However, mutations and overexpression of these genes are associated with malignancies. The mutations in KIT, PI۳K, and AKT genes are different from those found in other malignancies. Also, most of the drugs that inhibit the RTK signaling are being tested in clinical trials for the treatment of breast cancer. Monitoring and timely management of adverse effects are critical to minimize toxicities and optimize the efficacy of this targeted therapy. Therefore, further development of predictive biomarkers can better select patients who will benefit from RTK inhibitors.

AKT gene, Breast cancer, KIT gene, PI۳K gene, RTK signaling