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The expression of cancer-testis antigen in ovarian cancer and the development of immunotherapy

期刊

AMERICAN JOURNAL OF CANCER RESEARCH
卷 12, 期 2, 页码 681-694

出版社

E-CENTURY PUBLISHING CORP

关键词

Cancer-testis antigen; ovarian cancer; immunotherapy; MAGE-A/NY-ESO-1/CT45/Sp17

类别

资金

  1. NSFC [U20A20413]
  2. Natural Science Fund of Liaoning Province of China [2020-M S-141]
  3. Scientific Research Fund of Liaoning Provincial Education Department of China [QN2019-033]
  4. Major Special S&T Projects in Liaoning Province [2019JH1/10300005]
  5. Shenyang ST Projects [20-204-4-22, 19-109-4-09]
  6. Program for Shenyang High Level Talent Innovation and Entrepreneurship Team [2019-SYRCCY-B-01]
  7. Key Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Cancer of Ministry of Education (China Medical University)

向作者/读者索取更多资源

Ovarian cancer is a common and highly mortal tumor in the female reproductive system. It is often diagnosed at an advanced stage due to lack of apparent early symptoms and effective screening strategies. Immunotherapy using tumor-associated antigens shows promise in improving the treatment of ovarian cancer. Cancer-testis antigens (CTAs), including MAGE-A, NY-ESO-1, CT45, and Sp17, are highly expressed in ovarian cancer and are considered ideal targets for immunotherapy.
Ovarian cancer is a relatively common tumor in women with the highest mortality among female reproductive system tumors. The lack of apparent early symptoms and effective screening strategies often leads to ovarian cancer being diagnosed at an advanced stage. Immunotherapy relying on tumor-associated antigens might improve the treatment of ovarian cancer. Cancer-testis antigens (CTAs) are ideal tumor-associated antigens, and MAGE-A, NY-ESO-1, CT45, and Sp17 are classic CTAs highly expressed in ovarian cancer. Here, we review the research on CTAs in ovarian cancer, including prognostic value and advances in immunotherapy, all of which are essential for developing a theoretical basis for targeted therapy strategies.

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