软骨肉瘤
褪黑素
癌症研究
失巢
转移
基质金属蛋白酶
细胞生长
生物
癌变
医学
病理
内分泌学
癌症
生物化学
遗传学
作者
Nguyen Bao Tran,Chih‐Yang Lin,Ting‐Kuo Chang,Yi‐Chin Fong,Louis Anoop Thadevoos,Chao‐Yang Lai,Yuan‐Li Huang,Chang‐Hai Tsai,Chih‐Yuan Ko,Ju‐Fang Liu,Shun‐Fa Yang,Chih‐Hsin Tang
摘要
Chondrosarcoma has a high propensity to metastasize and responds poorly to chemotherapy and radiation treatment. The enzymatic activity of matrix metalloproteinases (MMPs) is very important in chondrosarcoma metastasis. Melatonin exhibits anticarcinogenic activity in many types of cancers by suppressing the expression of certain MMP family members, but this has not yet been clearly determined in chondrosarcoma. Our study demonstrates that MMP7 plays an essential role in chondrosarcoma cell proliferation, migration, and anoikis resistance. We also found that MMP7 is highly expressed in chondrosarcomas. Our in vitro and in vivo investigations show that melatonin strongly inhibits chondrosarcoma cell proliferation, migration, and anoikis resistance by directly suppressing MMP7 expression. Melatonin reduced MMP7 synthesis by promoting levels of miR-520f-3p expression, which were downregulated in human chondrosarcoma tissue samples. Pharmacological inhibition of miR-520f-3p markedly reversed the effects of melatonin upon chondrosarcoma proliferation and metastasis. Thus, our study suggests that melatonin has therapeutic potential for reducing the tumorigenesis and metastatic potential of chondrosarcoma via the miR-520f-3p/MMP7 axis.
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