Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
Cell Cycle. 2010 Jun 1;9(11):2118-23. doi: 10.4161/cc.9.11.11726.
A major goal of tumor suppressor research is to neutralize the tumorigenic effects of their loss. Since loss of pRb does not induce tumorigenesis in many types of cells, natural mechanisms may neutralize the tumorigenic effects of pRb loss in these cells. For susceptible cells, neutralizing the tumorigenic effects of pRb loss could logically be achieved by correcting the deregulated activities of pRb targets to render pRb-deficient cells less abnormal. This line of research has unexpectedly revealed that knocking out the pRb target Skp2 did not render Rb1 deficient cells less abnormal but, rather, induced apoptosis in them, thereby completely blocking tumorigenesis in Rb1+/- mice and after targeted deletion of Rb1 in pituitary intermediate lobe (IL). Skp2 is a substrate-recruiting component of the SCFSkp2 E3 biquitin ligase; one of its substrates is Thr187-phosphorylated p27Kip1. A p27T187A knockin (KI) mutation phenocopied Skp2 knockout (KO) in inducing apoptosis following Rb1 loss. Thus, Skp2 KO or p27T187A KI are synthetic lethal with pRb inactivation. Since homozygous p27T187A KI mutations show no adverse effects in mice, inhibiting p27T187 phosphorylation or p27T187p ubiquitination could be a highly therapeutic and minimally toxic intervention strategy for pRb deficiency-induced tumorigenesis.
肿瘤抑制因子研究的一个主要目标是中和其失活的致瘤效应。由于 pRb 的缺失并不会在许多类型的细胞中诱导肿瘤发生,因此自然机制可能会中和这些细胞中 pRb 缺失的致瘤效应。对于易感性细胞,通过纠正 pRb 靶标的失调活性,使 pRb 缺失的细胞不那么异常,从而逻辑上可以中和 pRb 缺失的致瘤效应。这条研究路线出人意料地揭示,敲除 pRb 靶标 Skp2 并没有使 Rb1 缺失的细胞不那么异常,而是诱导它们凋亡,从而完全阻断了 Rb1+/- 小鼠和垂体中间叶(IL)中 Rb1 靶向缺失后的肿瘤发生。Skp2 是 SCFSkp2 E3 泛素连接酶的底物募集成分;其底物之一是 Thr187 磷酸化的 p27Kip1。p27T187A 敲入(KI)突变在 Rb1 缺失后诱导凋亡,与 Skp2 敲除(KO)表现出相似的表型。因此,Skp2 KO 或 p27T187A KI 与 pRb 失活具有合成致死性。由于纯合子 p27T187A KI 突变在小鼠中没有不良影响,抑制 p27T187 磷酸化或 p27T187p 泛素化可能是一种针对 pRb 缺失诱导的肿瘤发生的高度治疗性和最小毒性干预策略。