Department of Oncology, University of Calgary, Calgary, Alberta, Canada.
Autophagy. 2013 Mar;9(3):413-4. doi: 10.4161/auto.22867. Epub 2013 Jan 15.
Multiple myeloma (MM) is a clonal plasma cell malignancy that accounts for 10-15% of newly diagnosed hematological cancers. Although significant advances have been made in the treatment of MM the disease still remains incurable. The oncolytic potential of reovirus has previously been demonstrated by others and us and is currently in phase III clinical trials for solid tumors. In addition a phase I clinical trial has recently been initiated for MM. Despite the clinical activity, the mechanism(s) of cell death caused by reovirus in MM is yet not yet well elucidated. A comprehensive understanding of reovirus-mediated histology-specific cell death mechanisms is imperative if this therapeutic is to become a standard of care for patients. Previously we have shown that reovirus-mediated cell death of breast and prostate cancer is orchestrated via apoptosis. The present study demonstrates for the first time that in addition to inducing apoptosis reovirus also upregulates autophagy during oncolysis of MM.
多发性骨髓瘤(MM)是一种克隆性浆细胞恶性肿瘤,占新发血液系统恶性肿瘤的 10-15%。尽管在 MM 的治疗方面取得了重大进展,但该病仍然无法治愈。其他人及我们已经证明了呼肠孤病毒的溶瘤潜力,目前正在进行针对实体瘤的 III 期临床试验。此外,最近还启动了一项针对 MM 的 I 期临床试验。尽管具有临床活性,但呼肠孤病毒在 MM 中引起细胞死亡的机制尚不清楚。如果这种治疗方法要成为患者的标准治疗方法,则需要全面了解呼肠孤病毒介导的组织特异性细胞死亡机制。以前我们已经表明,呼肠孤病毒介导的乳腺癌和前列腺癌细胞死亡是通过凋亡来协调的。本研究首次表明,除了诱导细胞凋亡外,呼肠孤病毒在 MM 的溶瘤过程中还会上调自噬。