Department of Orthopedics Surgery, The Provincial Hospital Affiliated to Shandong University, Shandong, China.
Biochem Biophys Res Commun. 2013 Sep 6;438(4):635-9. doi: 10.1016/j.bbrc.2013.07.131. Epub 2013 Aug 8.
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.
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。