Sabbatino Francesco, Wang Yangyang, Wang Xinhui, Schwab Joseph H, Ferrone Soldano, Ferrone Cristina R
Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Department Orthopaedic Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Semin Oncol. 2014 Oct;41(5):685-99. doi: 10.1053/j.seminoncol.2014.08.007. Epub 2014 Aug 12.
A growing body of experimental and clinical evidence strongly suggests that the resistance of cancer-initiating cells (CICs) to conventional therapies represents a major obstacle to the successful treatment of a malignant disease. To overcome this limitation a novel combinatorial tumor antigen (TA)-specific monoclonal antibody (mAb) strategy has been developed. In this strategy TA-specific mAbs are combined with chemotherapeutic agents and/or small molecules that inhibit aberrantly activated signaling pathways in cancer cells and especially in CICs. The in vitro results we have obtained indicate that this strategy is very effective in eradicating both differentiated cancer cells and CICs in several types of malignant disease. If the in vitro results have in vivo relevance, the strategy we have designed may have an impact on the treatment of malignant diseases.
越来越多的实验和临床证据有力地表明,癌症起始细胞(CICs)对传统疗法的抗性是成功治疗恶性疾病的主要障碍。为克服这一局限,已开发出一种新型组合肿瘤抗原(TA)特异性单克隆抗体(mAb)策略。在该策略中,TA特异性mAb与化疗药物和/或小分子相结合,这些化疗药物和小分子可抑制癌细胞尤其是CICs中异常激活的信号通路。我们获得的体外实验结果表明,该策略在根除多种恶性疾病中的分化癌细胞和CICs方面非常有效。如果体外实验结果具有体内相关性,那么我们设计的策略可能会对恶性疾病的治疗产生影响。