Role of SLC7A11/xCT in Ovarian Cancer.

Scientific Direction, IRCCS INRCA, 60124 Ancona, Italy. Hypertension and Cardiovascular Risk Research Center, Medical and Surgical Sciences Department, Alma Mater Studiorum University of Bologna, 40126 Bologna, Italy. Department of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, 60126 Ancona, Italy. Obstetrics and Gynecology Unit, Sant'Anna e San Sebastiano Hospital, 81100 Caserta, Italy. Department of Biomedical Sciences, Humanitas University, 20072 Milan, Italy. IRCCS Humanitas Research Hospital, 20089 Rozzano, Italy. Department of Experimental and Clinical Medicine, Università Politecnica delle Marche, 60126 Ancona, Italy.

International journal of molecular sciences. 2024;(1)
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Abstract

Ovarian cancer is one of the most dangerous gynecologic cancers worldwide and has a high fatality rate due to diagnosis at an advanced stage of the disease as well as a high recurrence rate due to the occurrence of chemotherapy resistance. In fact, chemoresistance weakens the therapeutic effects, worsening the outcome of this pathology. Solute Carrier Family 7 Member 11 (SLC7A11, also known as xCT) is the functional subunit of the Xc- system, an anionic L-cystine/L-glutamate antiporter expressed on the cell surface. SLC7A11 expression is significantly upregulated in several types of cancers in which it can inhibit ferroptosis and favor cancer cell proliferation, invasion and chemoresistance. SLC7A11 expression is also increased in ovarian cancer tissues, suggesting a possible role of this protein as a therapeutic target. In this review, we provide an overview of the current literature regarding the role of SLC7A11 in ovarian cancer to provide new insights on SLC7A11 modulation and evaluate the potential role of SLC7A11 as a therapeutic target.

Methodological quality

Publication Type : Review

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