De Maeyer-Guignard J, Lauret E, Eusèbe L, De Maeyer E
Centre National de la Recherche Scientifique, Unité de Recherche Associée 1343, Institut Curie, Orsay, France.
Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5708-12. doi: 10.1073/pnas.90.12.5708.
The Hyal-1 locus, which we have previously described and mapped to mouse chromosome 9, influences the serum levels and molecular weight forms of hyaluronidase. We have also shown that the growth of two transplantable tumors, the 3LL carcinoma and the B16F10 melanoma, is influenced by the alleles at Hyal-1, in that the tumors develop more slowly in congenic B6.C-Hyal-1a (also called HW23) mice than in the parental Hyal-1b C57BL/6 mice. Here we present evidence that tumor development is stimulated and mortality is accelerated in B6.C-Hyal-1a mice grafted with 3LL carcinoma cells when treated with alpha/beta interferon (IFN-alpha/beta) or with IFN-beta, whereas in IFN-treated C57BL/6 mice 3LL tumor growth is inhibited. Likewise, in B6.C-Hyal-1a mice grafted with B16F10 melanoma cells, IFN-alpha/beta treatment results in stimulation of tumor growth, whereas in IFN-treated C57BL/6 mice tumor growth, whereas in IFN-treated C57BL/6 mice tumor growth is inhibited and mortality delayed. Thus, IFN-alpha/beta treatment of B6.C-Hyal-1a mice results in stimulation of tumor development and sometimes in accelerated mortality. This is the opposite of the usually described effect of IFN treatment in mice, which is inhibition of tumor development and delayed mortality, as was indeed observed in the C57BL/6 mice in the present experiments. These results provide the first indication that host genes can up- or down-regulate the antitumor activity of IFN and that, on some genetic backgrounds, IFN treatment enhances rather than inhibits tumor development. This may help to explain the apparent discordance between mouse model studies, which hitherto have consistently reported inhibition of tumor formation by IFN, and the clinical trials, in which only a limited percentage of individuals show tumor regression while others have no beneficial effect or even have progression of disease in spite of the IFN treatment.
我们先前已描述过透明质酸酶1(Hyal-1)基因座并将其定位到小鼠9号染色体上,该基因座会影响透明质酸酶的血清水平和分子量形式。我们还表明,两种可移植肿瘤——3LL癌和B16F10黑色素瘤的生长受Hyal-1等位基因的影响,即与亲代Hyal-1b C57BL/6小鼠相比,3LL癌在同基因B6.C-Hyal-1a(也称为HW23)小鼠中生长更为缓慢。在此,我们提供证据表明,用α/β干扰素(IFN-α/β)或IFN-β处理接种3LL癌细胞的B6.C-Hyal-1a小鼠时,肿瘤发展会受到刺激且死亡率会加快,而在经IFN处理的C57BL/6小鼠中,3LL肿瘤生长受到抑制。同样,在接种B16F10黑色素瘤细胞的B6.C-Hyal-1a小鼠中,IFN-α/β处理会导致肿瘤生长受到刺激,而在经IFN处理的C57BL/6小鼠中肿瘤生长受到抑制且死亡率延迟。因此,对B6.C-Hyal-1a小鼠进行IFN-α/β处理会导致肿瘤发展受到刺激,有时还会加快死亡率。这与通常所描述的IFN对小鼠的作用相反,即在本实验中C57BL/6小鼠中观察到的IFN抑制肿瘤发展并延迟死亡率。这些结果首次表明宿主基因可以上调或下调IFN的抗肿瘤活性,并且在某些遗传背景下,IFN处理会增强而非抑制肿瘤发展。这可能有助于解释小鼠模型研究与临床试验之间明显的不一致,迄今为止小鼠模型研究一直报告IFN可抑制肿瘤形成,而在临床试验中,只有有限比例的个体显示肿瘤消退,而其他个体尽管接受了IFN治疗却没有有益效果甚至疾病进展。