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首页> 外文期刊>Critical reviews in oncology/hematology >The erythropoietin receptor in normal and cancer tissues.
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The erythropoietin receptor in normal and cancer tissues.

机译:正常组织和癌组织中的促红细胞生成素受体。

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摘要

The hormone erythropoietin (EPO) is essential for the survival, proliferation and differentiation of the erythrocytic progenitors. The EPO receptor (EPO-R) of erythrocytic cells belongs to the cytokine class I receptor family and signals through various protein kinases and STAT transcription factors. The EPO-R is also expressed in many organs outside the bone marrow, suggesting that EPO is a pleiotropic anti-apoptotic factor. The controversial issue as to whether the EPO-R is functional in tumor tissue is critically reviewed. Importantly, most studies of EPO-R detection in tumor tissue have provided falsely positive results because of the lack of EPO-R specific antibodies. However, endogenous EPO appears to be necessary to maintain the viability of endothelial cells and to promote tumor angiogenesis. Although there is no clinical proof that the administration of erythropoiesis stimulating agents (ESAs) promotes tumor growth and mortality, present recommendations are that (i) ESAs should be administeredat the lowest dose sufficient to avoid the need for red blood cell transfusions, (ii) ESAs should not be used in patients with active malignant disease not receiving chemotherapy or radiotherapy, (iii) ESAs should be discontinued following the completion of a chemotherapy course, (iv) the target Hb should be 12g/dL and not higher and (v) the risks of shortened survival and tumor progression have not been excluded when ESAs are dosed to target Hb <12g/dL.
机译:促红细胞生成素(EPO)激素对于促红细胞祖细胞的存活,增殖和分化至关重要。红细胞的EPO受体(EPO-R)属于I类细胞因子受体家族,通过各种蛋白激酶和STAT转录因子发出信号。 EPO-R还在骨髓以外的许多器官中表达,表明EPO是多效抗凋亡因子。关于EPO-R是否在肿瘤组织中起作用的有争议的问题已得到严格审查。重要的是,由于缺乏EPO-R特异性抗体,大多数在肿瘤组织中检测EPO-R的研究提供了假阳性结果。但是,内源性EPO似乎对于维持内皮细胞的活力并促进肿瘤血管生成是必需的。尽管尚无临床证据表明给予红细胞生成刺激剂(ESA)会促进肿瘤生长和死亡率,但目前的建议是(i)ESAs应以足以避免红细胞输血的最低剂量给药;(ii)对于未接受化学疗法或放射疗法的活动性恶性肿瘤患者,不应使用ESA;(iii)在完成化学疗程后应停止使用ESAs;(iv)目标Hb应为12g / dL,且不得更高;以及(v) ESA的目标Hb <12g / dL剂量时,并未排除缩短生存期和肿瘤进展的风险。

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