Peter MacCallum Cancer Centre, Melbourne, 3000, VIC, Australia.
Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, 3010, VIC, Australia.
Nat Commun. 2019 Mar 20;10(1):1295. doi: 10.1038/s41467-019-09312-9.
ABCB1 encodes Multidrug Resistance protein (MDR1), an ATP-binding cassette member involved in the cellular efflux of chemotherapeutic drugs. Here we report that ovarian and breast samples from chemotherapy treated patients are positive for multiple transcriptional fusions involving ABCB1, placing it under the control of a strong promoter while leaving its open reading frame intact. We identified 15 different transcriptional fusion partners involving ABCB1, as well as patients with multiple distinct fusion events. The partner gene selected depended on its structure, promoter strength, and chromosomal proximity to ABCB1. Fusion positivity was strongly associated with the number of lines of MDR1-substrate chemotherapy given. MDR1 inhibition in a fusion positive ovarian cancer cell line increased sensitivity to paclitaxel more than 50-fold. Convergent evolution of ABCB1 fusion is therefore frequent in chemotherapy resistant recurrent ovarian cancer. As most currently approved PARP inhibitors (PARPi) are MDR1 substrates, prior chemotherapy may precondition resistance to PARPi.
ABCB1 编码多药耐药蛋白(MDR1),这是一种参与化疗药物细胞外排的 ATP 结合盒成员。在这里,我们报告说,接受化疗治疗的卵巢和乳腺癌样本中存在涉及 ABCB1 的多种转录融合,这些融合将其置于强启动子的控制下,同时保持其开放阅读框完整。我们确定了 15 种不同的涉及 ABCB1 的转录融合伙伴,以及具有多种不同融合事件的患者。所选的伙伴基因取决于其结构、启动子强度和与 ABCB1 的染色体接近程度。融合阳性与给予的 MDR1 底物化疗线数密切相关。在融合阳性卵巢癌细胞系中抑制 MDR1 将紫杉醇的敏感性提高了 50 多倍。因此,ABCB1 融合的趋同进化在化疗耐药性复发性卵巢癌中非常常见。由于大多数目前批准的 PARP 抑制剂(PARPi)都是 MDR1 的底物,因此先前的化疗可能会使对 PARPi 的耐药性预先形成条件。