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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Identification of truncated chemokine receptor 7 in human colorectal cancer unable to localize to the cell surface and unreactive to external ligands.
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Identification of truncated chemokine receptor 7 in human colorectal cancer unable to localize to the cell surface and unreactive to external ligands.

机译:人结肠直肠癌中无法定位到细胞表面且对外部配体不反应的截短趋化因子受体7的鉴定。

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摘要

Chemokine receptors are thought to be involved in the process of cancer metastases. When investigating cell lines and tissues from colorectal cancer (CRC), the CCR7 protein unexpectedly was confined to the cytoplasm and not present on the cell surface. This study investigated at the DNA, mRNA and protein level, the mechanism and the consequences of the failure of CCR7 to localize to the cell membrane. In all 15 CRC cell lines tested, no surface CCR7 was detected and no chemotactic response was elicited upon in-vitro exposure to CCR7 chemokine ligands (CCL) 19 and CCL21. Integrity of CCR7 DNA and mRNA was examined with respect to signal peptide expression in cell lines and CRC tissues by real-time RT-PCR and sequencing. Nine of 15 CRC cell lines and 8 of 14 CRC tissues revealed a truncated CCR7 mRNA species containing various incomplete signal peptide encoding sequences, while the corresponding DNA was intact. These results indicate in CRC frequent alternative splicing or post-transcriptional mRNA modification resulting in a CCR7 molecule lacking an intact signal peptide prohibiting membrane translocation. Further studies would be necessary to identify a potential intracellular role of the truncated CCR7, abundantly present in the cytoplasm.
机译:趋化因子受体被认为与癌症转移过程有关。在调查来自大肠癌(CRC)的细胞系和组织时,CCR7蛋白出乎意料地局限于细胞质,并且不存在于细胞表面。这项研究在DNA,mRNA和蛋白质水平上研究了CCR7未能定位于细胞膜的机制及其后果。在所有测试的15种CRC细胞系中,在体外暴露于CCR7趋化因子配体(CCL)19和CCL21时,未检测到表面CCR7,也未引发趋化反应。关于CCR7 DNA和mRNA的完整性,通过实时RT-PCR和测序检查了细胞系和CRC组织中信号肽的表达。 15个CRC细胞系中的9个和14个CRC组织中的8个显示出截短的CCR7 mRNA物种,其中包含各种不完整的信号肽编码序列,而相应的DNA是完整的。这些结果表明在CRC中频繁进行选择性剪接或转录后mRNA修饰,导致CCR7分子缺少完整的信号肽,禁止膜移位。有必要进行进一步的研究以鉴定大量存在于细胞质中的截短的CCR7的潜在细胞内作用。

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