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首页> 外文期刊>British Journal of Cancer >Colocalisation of matrix metalloproteinase-9-mRNA and protein in human colorectal cancer stromal cells
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Colocalisation of matrix metalloproteinase-9-mRNA and protein in human colorectal cancer stromal cells

机译:基质金属蛋白酶-9-mRNA和蛋白质在人大肠癌基质细胞中的共定位

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The matrix metalloproteinases (MMPs) are perceived as essential for tumour invasion and metastases. The purpose of this study was to determine the expression and cellular localisation of the 92 kDa type IV collagenase (MMP-9) protein and mRNA in human colorectal cancer (CRC). In CRC and matched normal mucosa specimens from 26 CRC patients, Northern blot hybridisation and Western blot analyses provide convincing evidence that MMP-9 is expressed in greater quantities in CRC than in normal tissue. The MMP-9 tumour to normal mucosa fold-increase (T/N) was 9.7 +/- 7.1 (mean +/- s.d.) (P < 0.001) for RNA and 7.1 +/- 3.9 (P < 0.001) for protein. The sites of MMP-9 mRNA and protein synthesis were colocalised in tumour stroma by in situ hybridisation and immunohistochemistry in 26 CRC samples. Both MMP-9 mRNA and protein signals were strongest in the population of stromal cells concentrated at the tumour-stroma interface of an invading tumour. Furthermore, MMP-9-positive cells were identified as macrophages using an antimacrophage antibody (KP1) in serial sections from ten CRC samples. Given the persistent localisation of MMP-9-producing macrophages to the interphase between CRC and surrounding stroma, our observations suggest that MMP-9 production is controlled, in part, by tumour-stroma cell interactions. Further studies are needed to determine the in vivo regulation of MMP-9 production from infiltrating peritumour macrophages.
机译:基质金属蛋白酶(MMPs)被认为是肿瘤侵袭和转移所必需的。这项研究的目的是确定人类结肠直肠癌(CRC)中92 kDa IV型胶原酶(MMP-9)蛋白和mRNA的表达和细胞定位。在来自26位CRC患者的CRC和匹配的正常黏膜标本中,Northern blot杂交和Western blot分析提供了令人信服的证据,表明MMP-9在CRC中的表达量高于正常组织。 MMP-9肿瘤到正常粘膜倍增(T / N)的RNA为9.7 +/- 7.1(平均值+/- s.d.)(P <0.001),蛋白质为7.1 +/- 3.9(P <0.001)。通过原位杂交和免疫组织化学方法在26个CRC样本中将MMP-9 mRNA和蛋白质合成的位点共定位在肿瘤基质中。在侵袭性肿瘤的肿瘤-基质界面上集中的基质细胞群中,MMP-9 mRNA和蛋白质信号均最强。此外,使用抗巨噬细胞抗体(KP1)在来自十个CRC样本的连续切片中将MMP-9阳性细胞鉴定为巨噬细胞。鉴于产生MMP-9的巨噬细胞持续定位于CRC与周围基质之间的相间,我们的观察结果表明,MMP-9的产生部分受肿瘤-基质细胞相互作用的控制。需要进一步的研究来确定从浸润性肿瘤周围巨噬细胞产生的MMP-9的体内调节。

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