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Review Open Access

New use of microsatellite instability analysis in endometrial cancer (Review)

  • Authors:
    • Haruko Kunitomi
    • Kouji Banno
    • Megumi Yanokura
    • Takashi Takeda
    • Moito Iijima
    • Kanako Nakamura
    • Miho Iida
    • Masataka Adachi
    • Keiko Watanabe
    • Yusuke Matoba
    • Yusuke Kobayashi
    • Eiichiro Tominaga
    • Daisuke Aoki
  • View Affiliations / Copyright

    Affiliations: Department of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo 160‑8582, Japan
    Copyright: © Kunitomi et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 3297-3301
    |
    Published online on: July 20, 2017
       https://doi.org/10.3892/ol.2017.6640
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Abstract

The increasing incidence of obesity and diabetes due to changes in diet, earlier menarche, delayed menopause, late marriage, and declining birth rate have resulted in an increase in the number of endometrial cancer cases over the last few decades. Although surgical therapy is sufficient for early endometrial cancer, there is no effective therapy for patients with advanced and recurrent endometrial cancer. The oncogenic mechanism of endometrial cancer involves microsatellite instability (MSI) caused by dysfunction of DNA mismatch repair genes in 30% of patients. Immune checkpoint inhibitors, including anti‑programmed death (PD)‑1 and anti‑PD‑ligand 1 antibodies, are of interest as novel anticancer drugs; however, these drugs are currently expensive, and there is a need to select patients who will benefit from their use. The use of MSI analysis as a predictive biomarker for the therapeutic efficacy of these drugs may be useful for reducing the costs of drug therapy.
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Copy and paste a formatted citation
Spandidos Publications style
Kunitomi H, Banno K, Yanokura M, Takeda T, Iijima M, Nakamura K, Iida M, Adachi M, Watanabe K, Matoba Y, Matoba Y, et al: New use of microsatellite instability analysis in endometrial cancer (Review). Oncol Lett 14: 3297-3301, 2017.
APA
Kunitomi, H., Banno, K., Yanokura, M., Takeda, T., Iijima, M., Nakamura, K. ... Aoki, D. (2017). New use of microsatellite instability analysis in endometrial cancer (Review). Oncology Letters, 14, 3297-3301. https://doi.org/10.3892/ol.2017.6640
MLA
Kunitomi, H., Banno, K., Yanokura, M., Takeda, T., Iijima, M., Nakamura, K., Iida, M., Adachi, M., Watanabe, K., Matoba, Y., Kobayashi, Y., Tominaga, E., Aoki, D."New use of microsatellite instability analysis in endometrial cancer (Review)". Oncology Letters 14.3 (2017): 3297-3301.
Chicago
Kunitomi, H., Banno, K., Yanokura, M., Takeda, T., Iijima, M., Nakamura, K., Iida, M., Adachi, M., Watanabe, K., Matoba, Y., Kobayashi, Y., Tominaga, E., Aoki, D."New use of microsatellite instability analysis in endometrial cancer (Review)". Oncology Letters 14, no. 3 (2017): 3297-3301. https://doi.org/10.3892/ol.2017.6640
Copy and paste a formatted citation
x
Spandidos Publications style
Kunitomi H, Banno K, Yanokura M, Takeda T, Iijima M, Nakamura K, Iida M, Adachi M, Watanabe K, Matoba Y, Matoba Y, et al: New use of microsatellite instability analysis in endometrial cancer (Review). Oncol Lett 14: 3297-3301, 2017.
APA
Kunitomi, H., Banno, K., Yanokura, M., Takeda, T., Iijima, M., Nakamura, K. ... Aoki, D. (2017). New use of microsatellite instability analysis in endometrial cancer (Review). Oncology Letters, 14, 3297-3301. https://doi.org/10.3892/ol.2017.6640
MLA
Kunitomi, H., Banno, K., Yanokura, M., Takeda, T., Iijima, M., Nakamura, K., Iida, M., Adachi, M., Watanabe, K., Matoba, Y., Kobayashi, Y., Tominaga, E., Aoki, D."New use of microsatellite instability analysis in endometrial cancer (Review)". Oncology Letters 14.3 (2017): 3297-3301.
Chicago
Kunitomi, H., Banno, K., Yanokura, M., Takeda, T., Iijima, M., Nakamura, K., Iida, M., Adachi, M., Watanabe, K., Matoba, Y., Kobayashi, Y., Tominaga, E., Aoki, D."New use of microsatellite instability analysis in endometrial cancer (Review)". Oncology Letters 14, no. 3 (2017): 3297-3301. https://doi.org/10.3892/ol.2017.6640
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