Tai Yu-Tzu, Anderson Kenneth C
Oncotarget. 2012 Sep;3(9):913-4. doi: 10.18632/oncotarget.655.
Our findings therefore provide a strong rationale for investigating Btk inhibitors in MM and WM to target both tumor cells and their supporting BM microenvironment and thereby both suppress tumor cell growth and abrogate MM-induced bone disease.
因此,我们的研究结果为在多发性骨髓瘤和华氏巨球蛋白血症中研究布鲁顿酪氨酸激酶(Btk)抑制剂提供了有力的理论依据,以靶向肿瘤细胞及其支持性骨髓微环境,从而既抑制肿瘤细胞生长,又消除多发性骨髓瘤引起的骨病。