4.6 Review

Therapeutic Strategies Focused on Cancer-Associated Hypercoagulation for Ovarian Clear Cell Carcinoma

期刊

CANCERS
卷 14, 期 9, 页码 -

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MDPI
DOI: 10.3390/cancers14092125

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ovarian clear cell carcinoma; tissue factor; IL6; D-dimer; cancer-associated thrombosis; inflammation; hypoxia; tisotumab vedotin; immunotherapy

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Ovarian clear cell carcinoma (OCCC) is characterized by chemotherapy resistance and poor prognosis, especially in advanced cases. This review focuses on the association between cancer-associated hypercoagulation and molecular biology in OCCC. Additionally, potential drug therapies targeting hypercoagulation for OCCC are summarized. The review is expected to contribute to novel research and trials for the prevention, early detection, and treatment of OCCC.
Simple Summary Ovarian clear cell carcinoma (OCCC) has a poor prognosis in advanced cases and displays resistance to standard treatments for epithelial ovarian cancer. OCCC shows a specific clinical characteristic of a high incidence of cancer-associated thromboembolism. In this review, we focused on the association between cancer-related hypercoagulation and molecular biology in OCCC. Moreover, we summarized potential drugs targeting hypercoagulation to contribute to novel therapies for OCCC. Ovarian clear cell carcinoma (OCCC) is associated with chemotherapy resistance and poor prognosis, especially in advanced cases. Although comprehensive genomic analyses have clarified the significance of genomic alterations such as ARID1A and PIK3CA mutations in OCCC, therapeutic strategies based on genomic alterations have not been confirmed. On the other hand, OCCC is clinically characterized by a high incidence of thromboembolism. Moreover, OCCC specifically shows high expression of tissue factor and interleukin-6, which play a critical role in cancer-associated hypercoagulation and may be induced by OCCC-specific genetic alterations or the endometriosis-related tumor microenvironment. In this review, we focused on the association between cancer-associated hypercoagulation and molecular biology in OCCC. Moreover, we reviewed the effectiveness of candidate drugs targeting hypercoagulation, such as tissue factor- or interleukin-6-targeting drugs, anti-inflammatory drugs, anti-hypoxia signaling drugs, anticoagulants, and combined immunotherapy with these drugs for OCCC. This review is expected to contribute to novel basic research and clinical trials for the prevention, early detection, and treatment of OCCC focused on hypercoagulation.

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