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首页> 外文期刊>Journal of Pathology: Journal of the Pathological Society of Great Britain and Ireland >The hypoxia-regulated transcription factor DEC1 (Stra13, SHARP-2) and its expression in human tissues and tumours.
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The hypoxia-regulated transcription factor DEC1 (Stra13, SHARP-2) and its expression in human tissues and tumours.

机译:低氧调节的转录因子DEC1(Stra13,SHARP-2)及其在人体组织和肿瘤中的表达。

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摘要

DEC1, also known as SHARP-2 or Stra13, is an important molecule in embryonic differentiation and has recently been identified to be strongly inducible by hypoxia. Its distribution in normal human tissues and most tumour types is unknown. In the present study, a polyclonal antiserum to a 10-amino acid peptide from DEC1 has been raised. Using this antiserum, DEC1 was shown to be widely expressed in most normal human tissues, but usually only in a proportion of cells and typically with a nuclear localization. In tumours, expression was either augmented (the commonest pattern) or occasionally decreased. Similarly, in most normal tissues, low or absent expression was observed in endothelial cells, whereas in many tumour samples endothelium was usually strongly positive. In tumours, there was a striking pattern of staining seen in connection with areas of necrosis, with absence of DEC1 expression within a zone of morphologically viable cells immediately adjacent to the necrotic zone. This suggests that whileDEC1 may be up-regulated by hypoxia in cancer, in more extreme hypoxia it may have a role in cell death. Its interrelationship with other hypoxically regulated molecules, such as the hypoxia-inducible factors or carbonic anhydrase IX, and differentiation of tumours now requires further investigation.
机译:DEC1,也称为SHARP-2或Stra13,是胚胎分化中的重要分子,最近已被确定为可被缺氧强烈诱导。其在正常人组织和大多数肿瘤类型中的分布是未知的。在本研究中,已经提出了针对来自DEC1的10个氨基酸的肽的多克隆抗血清。使用这种抗血清,DEC1已显示在大多数正常人组织中广泛表达,但通常仅在一定比例的细胞中表达,并且通常具有核定位。在肿瘤中,表达要么增强(最常见的模式),要么偶尔降低。类似地,在大多数正常组织中,在内皮细胞中观察到低或无表达,而在许多肿瘤样品中,内皮通常是强阳性的。在肿瘤中,与坏死区域相关的染色明显,在紧邻坏死区域的形态学上有活力的细胞区域内没有DEC1表达。这表明尽管DEC1可能在癌症中被缺氧所上调,但在更极端的缺氧中它可能在细胞死亡中起作用。它与其他低氧调节分子(如低氧诱导因子或碳酸酐酶IX)之间的相互关系以及肿瘤的分化现在需要进一步研究。

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