德诺苏马布
破骨细胞
兰克尔
骨溶解
医学
骨转移
癌症研究
乳腺癌
转移
骨吸收
机制(生物学)
癌症
骨重建
后天抵抗
双膦酸盐
肿瘤科
骨密度保护剂
雌激素
内科学
骨质疏松症
生物信息学
乳腺癌转移
唑来膦酸
成骨细胞
作者
Q F Lin,Jinpeng Luo,Zhuxi Duan,Jieer Luo,Wei Zhang,Yuan Xia,Yinduo Zeng,Xiaolin Fang,J-J Liang,Jiayi Chen,Q F Lin,Yilin Quan,Ruiyu Hu,Hongcai Liu,Qiang Liu,Jun Li,Chang Gong
摘要
Bone metastasis remains a major cause of morbidity in estrogen receptor-positive breast cancer, with RANKL inhibitor resistance emerging as a critical clinical challenge. Nearly 40% of patients develop progressive skeletal lesions despite denosumab therapy, highlighting an urgent need to identify resistance mechanisms and alternative therapeutic strategies. We identified a RANKL-independent osteoclast activation pathway mediated by the CRKL/circCCDC50/NFATc1 axis. Mechanistically, CRKL promoted EIF4A3-dependent circCCDC50 biogenesis, which was packaged into large oncosomes and transferred to osteoclast precursors. Nuclear circCCDC50 recruited CARM1 to epigenetically activate NFATc1 transcription, establishing a self-reinforcing loop that sustained osteolysis despite RANKL blockade. Pharmacological inhibition of CARM1 (TP-064) effectively suppressed osteoclastogenesis and bone metastasis in denosumab-resistant models. These findings revealed a targetable resistance mechanism and provided a clinically actionable strategy to overcome microenvironment-driven metastasis through dual targeting of tumor and bone niches.
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