CEA, Institute of Emerging Diseases and Innovative Therapies (iMETI), F-92265 Fontenay-aux-Roses, France.
Département de biologie médicale, Hôpital Mignot, F-78150 Le Chesnay, France.
Nature. 2015 Sep 17;525(7569):380-3. doi: 10.1038/nature15248. Epub 2015 Sep 2.
Whether cancer is maintained by a small number of stem cells or is composed of proliferating cells with approximate phenotypic equivalency is a central question in cancer biology. In the stem cell hypothesis, relapse after treatment may occur by failure to eradicate cancer stem cells. Chronic myeloid leukaemia (CML) is quintessential to this hypothesis. CML is a myeloproliferative disorder that results from dysregulated tyrosine kinase activity of the fusion oncoprotein BCR-ABL. During the chronic phase, this sole genetic abnormality (chromosomal translocation Ph(+): t(9;22)(q34;q11)) at the stem cell level causes increased proliferation of myeloid cells without loss of their capacity to differentiate. Without treatment, most patients progress to the blast phase when additional oncogenic mutations result in a fatal acute leukaemia made of proliferating immature cells. Imatinib mesylate and other tyrosine kinase inhibitors (TKIs) that target the kinase activity of BCR-ABL have improved patient survival markedly. However, fewer than 10% of patients reach the stage of complete molecular response (CMR), defined as the point when BCR-ABL transcripts become undetectable in blood cells. Failure to reach CMR results from the inability of TKIs to eradicate quiescent CML leukaemia stem cells (LSCs). Here we show that the residual CML LSC pool can be gradually purged by the glitazones, antidiabetic drugs that are agonists of peroxisome proliferator-activated receptor-γ (PPARγ). We found that activation of PPARγ by the glitazones decreases expression of STAT5 and its downstream targets HIF2α and CITED2, which are key guardians of the quiescence and stemness of CML LSCs. When pioglitazone was given temporarily to three CML patients in chronic residual disease in spite of continuous treatment with imatinib, all of them achieved sustained CMR, up to 4.7 years after withdrawal of pioglitazone. This suggests that clinically relevant cancer eradication may become a generally attainable goal by combination therapy that erodes the cancer stem cell pool.
癌症是由少数干细胞维持的,还是由具有近似表型等效性的增殖细胞组成,这是癌症生物学中的一个核心问题。在干细胞假说中,治疗后复发可能是由于未能根除癌症干细胞所致。慢性髓系白血病(CML)是该假说的典型代表。CML 是一种骨髓增生性疾病,由融合致癌蛋白 BCR-ABL 的酪氨酸激酶活性失调引起。在慢性期,这种单一的遗传异常(干细胞水平的染色体易位 Ph(+): t(9;22)(q34;q11))导致髓系细胞过度增殖,而不丧失其分化能力。未经治疗,大多数患者会进展为急变期,此时额外的致癌突变导致由增殖未成熟细胞组成的致命急性白血病。甲磺酸伊马替尼和其他针对 BCR-ABL 激酶活性的酪氨酸激酶抑制剂(TKI)显著改善了患者的生存。然而,只有不到 10%的患者达到完全分子缓解(CMR)的阶段,定义为血液细胞中 BCR-ABL 转录本无法检测到的阶段。未能达到 CMR 是由于 TKI 无法根除静止的 CML 白血病干细胞(LSCs)。在这里,我们表明,残留的 CML LSC 池可以通过过氧化物酶体增殖物激活受体-γ(PPARγ)激动剂,即抗糖尿病药物格列酮逐渐清除。我们发现,格列酮激活 PPARγ会降低 STAT5 及其下游靶标 HIF2α 和 CITED2 的表达,这是 CML LSCs 静止和干性的关键保护者。当在慢性残留疾病中给三名 CML 患者暂时给予吡格列酮时,尽管他们一直在接受伊马替尼治疗,但他们都实现了持续的 CMR,在停用吡格列酮后长达 4.7 年。这表明通过侵蚀癌症干细胞池的联合治疗,临床上相关的癌症根除可能成为一个普遍可实现的目标。