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JS-K, a nitric oxide donor, induces autophagy as a complementary mechanism inhibiting ovarian cancer.

Bin Liu | Xiaojie Huang | Yifang Li | Weiguo Liao | Mingyi Li | Yi Liu | Rongrong He | Du Feng | Runzhi Zhu | Hiroshi Kurihara
BMC cancer | 2019

Ovarian cancer (OC) is the second most frequent gynecological cancer and is associated with a poor prognosis because OC progression is often asymptoma-tic and is detected at a late stage. There remains an urgent need for novel targeted therapies to improve clinical outcomes in ovarian cancer. As a nitric oxide prodrug, JS-K is reported highly cytotoxic to human cancer cells such as acute myeloid leukemia, multiple myeloma and breast cancer. This study is aim to investigate the influence of JS-K on proliferation and apoptosis in ovarian cancer cells and explored possible autophagy-related mechanisms, which will contribute to future ovarian cancer therapy and supply theory support that JS-K holds great promise as a novel therapeutic agent against ovarian cancer.

Pubmed ID: 31262254

Associated grants

None

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