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Evaluation of the Gene Encoding Carnitine Transporter (Octn2/Slc22a5) Expression in Human Breast Cancer and Its Association With Clinicopathological Characteristics Publisher Pubmed



Dinarvand N1, 6 ; Karimi F2 ; Azizi R3 ; Rastaghi S4 ; Sheikhi A5 ; Pourfarzam M6
Authors
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Authors Affiliations
  1. 1. Hyperlipidemia Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  2. 2. Department of Physiology, Behbahan Faculty of Medical Sciences, Behbahan, Iran
  3. 3. Molecular and Medicine Research Center, Khomein University of Medical Sciences, Khomein, Iran
  4. 4. Department of Biostatistics, School of Public Health, Mashhad University of Medical Sciences, Mashhad, Iran
  5. 5. Department of Immunology, School of Medicine, Dezful University of Medical Sciences, Dezful, Iran
  6. 6. Department of Clinical Biochemistry, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Molecular Biology Reports Published:2023


Abstract

Background: Fatty acid oxidation (FAO) is a major energy-generating process in the mitochondria and supports proliferation, growth, and survival of cancer cells. l-Carnitine is an essential co-factor for carrying long-chain fatty acids into the mitochondria. The entry of l-carnitine across cell membrane is regulated by OCTN2 (SLC22A5). Thus, it can plays a significant role in the mitochondrial fatty acid oxidation. This study aimed to evaluate the OCTN2 expression and its association with clinicopathological characteristics in breast cancer. Methods: In this work, OCTN2 was examined in 54 pairs of fresh samples of breast cancer (BC) and adjacent noncancerous tissue using quantitative real-time polymerase chain reaction and immunohistochemistry (IHC). The IHC approach was also used to investigate the expression of additional clinicopathological features. Results: The present research findings revealed that the relative expression of OCTN2 in BC tissues was substantially higher than the adjacent normal tissues. This up-regulation was correlated positively with tumor size and Ki-67 and negatively with the progesterone receptor (PR) status, providing evidence of the opposite effects of OCTN2 and PR on tumor development. Conclusion: The study shows that the OCTN2 expression in BC patients may be used as a prognostic biomarker and a tumor oncogene. As a result, it could be considered a possible therapeutic target. Nevertheless, the significance of the findings needs to be confirmed by further studies. © 2022, The Author(s), under exclusive licence to Springer Nature B.V.