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Runx2 通过转录抑制 TSSC1 诱导骨骨溶解。

Runx2 induces bone osteolysis by transcriptional suppression of TSSC1.

机构信息

Department of Orthopedics Surgery, The Provincial Hospital Affiliated to Shandong University, Shandong, China.

出版信息

Biochem Biophys Res Commun. 2013 Sep 6;438(4):635-9. doi: 10.1016/j.bbrc.2013.07.131. Epub 2013 Aug 8.

Abstract

Advanced breast cancers frequently metastasize to bone, resulting in osteolytic lesions, however, the underlying mechanisms are poorly understood. Runx2, a bone-specific transcriptional factor, is abnormally expressed in highly metastatic breast cancer cells. Here, we found that TSSC1 inhibits breast cancer cell invasion. Subsequently, TSSC1 is confirmed as a target of Runx2 and is negatively regulated by Runx2. Furthermore, overexpression of Runx2 induces bone osteolysis in a TSSC1-dependent manner. Our results may provide a strategy for the treatment of breast cancer and the prevention of skeletal metastasis.

摘要

晚期乳腺癌常转移至骨骼,导致溶骨性病变,但其中的潜在机制尚不清楚。Runx2 是一种骨骼特异性转录因子,在高转移性乳腺癌细胞中异常表达。在这里,我们发现 TSSC1 可抑制乳腺癌细胞侵袭。随后,证实 TSSC1 是 Runx2 的靶标,并受 Runx2 负调控。此外,Runx2 的过表达以 TSSC1 依赖的方式诱导骨溶骨。我们的研究结果可能为治疗乳腺癌和预防骨骼转移提供一种策略。

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