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Radiosensitization with combined use of olaparib and PI-103 in triple-negative breast cancer

机译:放射增敏联合奥拉帕尼和PI-103在三阴性乳腺癌中的应用

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摘要

BackgroundTriple-negative breast cancer (TNBC) shows aggressive clinical behavior, but the treatment options are limited due to lack of a specific target. TNBC shares many clinical and pathological similarities with BRCA-deficient breast cancer, for which poly(ADP-ribose) polymerase (PARP) inhibitor is effective, but PARP inhibitor alone failed to show clinical effects in patients with sporadic TNBC. Radiation induces DNA double-strand breaks, and the phosphoinositide 3-kinase (PI3K) signaling pathway has been known to regulate steady-state levels of homologous recombination. A recent preclinical study showed that PI3K inhibition impairs BRCA1/2 expression and sensitizes BRCA-proficient TNBC to PARP inhibition. Therefore, we assessed the radiosensitizing effect, and the underlying mechanism of combination treatment with PARP inhibitor olaparib and PI3K inhibitor PI-103 in BRCA-proficient TNBC cells.
机译:背景三阴性乳腺癌(TNBC)表现出侵略性的临床行为,但由于缺乏特异性靶标,治疗选择受到限制。 TNBC与BRCA缺乏型乳腺癌有许多临床和病理相似之处,其中聚(ADP-核糖)聚合酶(PARP)抑制剂有效,但单独的PARP抑制剂不能在散发性TNBC患者中显示临床效果。辐射诱导DNA双链断裂,并且已知磷酸肌醇3激酶(PI3K)信号传导途径可调节稳态水平的同源重组。最近的临床前研究表明,PI3K抑制作用会削弱BRCA1 / 2的表达,并使BRCA熟练的TNBC对PARP抑制作用敏感。因此,我们评估了BRCA敏感的TNBC细胞的放射增敏作用以及与PARP抑制剂olaparib和PI3K抑制剂PI-103联合治疗的潜在机制。

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