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RUNX1-Regulated Signaling Pathways in Ovarian Cancer

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BIOMEDICINES
卷 11, 期 9, 页码 -

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MDPI
DOI: 10.3390/biomedicines11092357

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Runt-related transcription factor 1 (RUNX1); ovarian cancer; apoptosis; signaling pathways; clinical therapeutic target

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Ovarian cancer is a leading cause of gynecological death worldwide, and RUNX1 plays an important role in its occurrence, development, and response to therapy. Decreased expression of RUNX1 improves chemotherapy sensitivity and provides support for diagnosis and treatment of ovarian cancer. However, the role of RUNX1 in ovarian cancer needs further investigation.
Ovarian cancer is the leading cause of gynecological death worldwide, and its poor prognosis and high mortality seriously affect the life of ovarian cancer patients. Runt-related transcription factor 1 (RUNX1) has been widely studied in hematological diseases and plays an important role in the occurrence and development of hematological diseases. In recent years, studies have reported the roles of RUNX1 in solid tumors, including the significantly increased expression of RUNX1 in ovarian cancer. In ovarian cancer, the dysregulation of the RUNX1 signaling pathway has been implicated in tumor progression, metastasis, and response to therapy. At the same time, the decreased expression of RUNX1 in ovarian cancer can significantly improve the sensitivity of clinical chemotherapy and provide theoretical support for the subsequent diagnosis and treatment target of ovarian cancer, providing prognosis and treatment options to patients with ovarian cancer. However, the role of RUNX1 in ovarian cancer remains unclear. Therefore, this article reviews the relationship between RUNX1 and the occurrence and development of ovarian cancer, as well as the closely regulated signaling pathways, to provide some inspiration and theoretical support for future research on RUNX1 in ovarian cancer and other diseases.

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